Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Effect: The variant's effect on the function of the gene/protein, displayed in the format 'R/C'. R is the value reported by the source (publication, submitter) and this classification may vary between records. C is the value concluded by the curator. Note that in some database the curator uses Summary records to give details on the classification of the variant.Values used: '+' indicating the variant affects function, '+?' probably affects function, '-' does not affect function, '-?' probably does not affect function, '?' effect unknown, '.' effect was not classified.
Exon: number of exon/intron containing variant; 2 = exon 2, 12i = intron 12, 2i_7i = from intron 2 to intron 7, 8i_9 = intron 8/exon 9 boundary, _1 = 5' to exon 1, 18_ = 3' of exon 18, _1_18_ = encompassing the entire 18-exon gene
DNA change (cDNA): description of variant at DNA level, based on a coding DNA reference sequence (following HGVS recommendations); e.g. c.123C>T, c.123_145del, c.123_126dup. For deletions/duplications extending beyond the reference transcript resp. {0}/{2} is used to replace del/dup. Extent of the deletion/duplication should be specified using the genomic description (g.). "-" indicates the variant described on genomic level does not affect the coding DNA reference sequence.
RNA change: description of variant at RNA level (following HGVS recommendations).
- r.123c>u
- r.? = unknown
- r.(?) = RNA not analysed but probably transcribed copy of DNA variant
- r.spl? = RNA not analysed but variant probably affects splicing
- r.(spl?) = RNA not analysed but variant may affect splicing
- r.0? = change expected to abolish transcription
Protein: description of variant at protein level (following HGVS recommendations).
- p.(Arg345Pro) = change predicted from DNA (RNA not analysed)
- p.Arg345Pro = change derived from RNA analysis
- p.? = unknown effect
- p.0? = probably no protein produced
Allele: On which allele is the variant located? Does not necessarily imply inheritance! 'Paternal' (confirmed or inferred), 'Maternal' (confirmed or inferred), 'Parent #1' or #2 for compound heterozygosity without having screened the parents, 'Unknown' for heterozygosity without having screened the parents, 'Both' for homozygozity.
Classification method: The method used for the clinical classification of this variant.
All options:
- ACMG
- ACGS
- EAHAD-CFDB
- ENIGMA
- IARC
- InSiGHT
- kConFab
- other
Clinical classification: Clinical classification of variant, preferably based on standardised criteria (e.g. ACMG), directed on the clinical consequences as published/submitted, indicated using an enriched system including inheritance: e.g. pathogenic, pathogenic (dominant), pathogenic (recessive), pathogenic (!), pathogenic (maternal), pathogenic (paternal). Standard inheritance is covered by dominant/recessive, imprinting by maternal/paternal. A '!' warns for exceptional circumstances to be explained in the 'Remarks' field (low penetrance, variants pathogenic in heterozygous state only, hypomorphic/hypermorphic variants, protective variants, etc.). Non-disease consequences (e.g. drug metabolism (pharmacogenetics), risk factor, blood group, tasting bitter) are indicated using additions to the benign classification; benign (dominant), benign (recessive), benign (!), etc. The value 'association' is used for variants associated with a phenotype and 'NA' for variants from in vitro/in silico records. NOTE: classification may differ from the opinion of the curator as given in a variant SUMMARY-record or the 'Functional effect concluded'). NOTE: pathogenic/likely pathogenic should go together with "variant (probably) affects function" In ClassFunctional.
All options:
- pathogenic
- pathogenic (dominant)
- pathogenic (recessive)
- pathogenic (!)
- pathogenic (maternal)
- pathogenic (paternal)
- likely pathogenic
- likely pathogenic (dominant)
- likely pathogenic (recessive)
- likely pathogenic (!)
- likely pathogenic (maternal)
- likely pathogenic (paternal)
- VUS
- VUS (!)
- likely benign
- likely benign (dominant)
- likely benign (recessive)
- likely benign (!)
- likely benign (maternal)
- likely benign (paternal)
- benign
- benign (dominant)
- benign (recessive)
- benign (!)
- benign (maternal)
- benign (paternal)
- association
- unclassified
- NA
DNA change (genomic) (hg19): HGVS description of variant at DNA level, based on the genomic (chromosomal) DNA reference sequence; e.g. g.12345678C>T, g.12345679del, g.12345678_12345890dup
DNA change (hg38): HGVS description of variant at DNA level, based on the hg38 genomic (chromosomal) eference sequence; e.g. g.12345678C>T, g.12345679del, g.12345678_12345890dup
Published as: listed only when different from "DNA change"; variant as reported originally (e.g. 521delT). Variants seen in animal models, tested in vitro, predicted from RNA analysis, etc. are described between brackets like c.(456C>G)
ISCN: description of the variant according to ISCN nomenclature
DB-ID: database ID of variant, grouping multiple observations of the same variant together, starting with the HGNC gene symbol, followed by an underscore (_) and a six digit number (e.g. DMD_012345). _000000 is used for variants where DNA was not analysed (change predicted from RNA analysis), variants seen in animal models or variants not seen in humans but functionally tested in vitro
Variant remarks: remarks regarding variant described, e.g. germline mosaicism in mother, 345 kb deletion, muscle RNA analysed, not in 200 control chromosomes tested, on founder haplotype, etc.
Reference: publication describing the variant submitted, incl. links to OMIM, PubMed or other source, e.g. "den Dunnen ASHG2003 P2346"
ClinVar ID: ID of variant in ClinVar database
dbSNP ID: the dbSNP ID
Origin: Origin of variant/record: Germline = in all cells, De novo = in all cells, but not in either parent, Germline/De novo (untested) = in all cells, parents not tested (use only when De novo is likely, e.g. isolated/sporadic cases with dominant disease), Somatic = present in a subset of cells, but not in either parent, Uniparental disomy = from parental disomy (maternal or paternal), CLASSIFICATION record = submitter only sharing variant classification (note another report may share Individual data), SUMMARY record = master summary record from curator (may link to another database), In vitro (cloned) = data resulting from in vitro functional assays, animal model = data from animal model, Artefact = false positive variant call, DUPLICATE record = variant already described on another chromosome (e.g. unbalanced translocation, duplicating transposition, 2nd fusion transcript, etc.)
All options:
- Germline
- De novo
- Germline/De novo (untested)
- Somatic
- Uniparental disomy
- Uniparental disomy, maternal allele
- Uniparental disomy, paternal allele
- CLASSIFICATION record
- SUMMARY record
- In vitro (cloned)
- In silico
- animal model
- Artefact
- DUPLICATE record
- Unknown
- Not applicable
Segregation: Indicates whether the variant segregates with the phenotype (yes), does not segregate with the phenotype (no) or segregation is unknown (?)
All options:
- ? = unknown
- yes = segregates with phenotype
- no = does not segregate with phenotype
- - = not applicable
Frequency: frequency in which the variant was found; e.g 5/760 chromosomes (in 5 of 760 chromosomes tested), 1/33 patients (in 1 of 33 patients analysed in study), 0.05 controls (in 5% of control cases tested)
Re-site: restriction enzyme recognition site created (+) or destroyed (-); e.g. BglII+;BamHI-
VIP: variant VIP-status was requested for matchmaking - need collaboration(s) to crack the case - please contact the submitter/curator.
NOTE: to get VIP status ask the curator.
Methylation: result of methylation test; GOM (gain of methylation), LOM (loss of methylation), 30% (30% methylated). NOTE: when several tests were done mention the method as well (e.g. MS-PCR 75%)

 Effect
|

 Exon
|

 DNA change (cDNA)
|

 RNA change
|

 Protein
|

 Classification method
|

 Clinical classification
|

 DNA change (genomic) (hg19)
|

 DNA change (hg38)
|

 Published as
|

 ISCN
|

 DB-ID
|
 Variant remarks
|

 Reference
|

 ClinVar ID
|

 dbSNP ID
|

 Origin
|

 Segregation
|

 Frequency
|

 Re-site
|

 VIP
|

 Methylation
|

 Owner
|
+/. |
- |
c.-506041_*1935315del |
r.0 |
p.0 |
- |
pathogenic (dominant) |
g.92414689_94864863del |
- |
chr5:92,414,689-94,864,863 (hg19/GRCh37) |
- |
NR2F1_000063 |
- |
PubMed: Rech 2020 |
- |
- |
Germline |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.-325733_*639854del |
r.0 |
p.0 |
- |
pathogenic (dominant) |
g.92594997_93569402del |
- |
chr5:92,594,997-93,569,402 (hg19) |
- |
NR2F1_000064 |
- |
PubMed: Rech 2020 |
- |
- |
Unknown |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
_1_3_ |
c.-1687_*240{0} |
r.0 |
p.0 |
- |
pathogenic (dominant) |
g.(?_92845157)_(93679748_?)del |
- |
92845157–93679748del |
- |
NR2F1_000043 |
0.83 Mb deletion; variant on paternal allele, father (unaffected) not avialable |
PubMed: Bosch 2014, Journal: Bosch 2014 |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Marc Ferre |
+/. |
_1_3_ |
c.-1687_*240{0} |
r.0 |
p.0 |
- |
pathogenic (dominant) |
g.(?_91064110)_(93896378_?)del |
- |
91064110–93896378del |
- |
NR2F1_000006 |
2.85 Mb deletion |
PubMed: Bosch 2014, Journal: Bosch 2014 |
- |
- |
De novo |
yes |
- |
- |
- |
- |
Marc Ferre |
+?/. |
_1_3_ |
c.-1687_*240{0} |
r.0 |
p.0 |
- |
likely pathogenic (dominant) |
g.(?_92856299)_(93054636_?)del |
- |
92856299_93054636 del |
- |
NR2F1_000043 |
0.2Mb deletion |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
_1_3_ |
c.-1687_*240{0} |
r.0 |
p.0 |
- |
likely pathogenic (dominant) |
g.(?_92910393)_(93806933_?)del |
- |
92910393_93806933del |
- |
NR2F1_000043 |
0.9Mb deletion |
PubMed: Chen 2016 |
- |
- |
Unknown |
yes |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
_1_3_ |
c.-1687_*240{0} |
r.0 |
p.0 |
- |
likely pathogenic (dominant) |
g.(?_92910393)_(93806933_?)del |
- |
- |
- |
NR2F1_000043 |
0.9Mb deletion |
PubMed: Chen 2016 |
- |
- |
Uniparental disomy, paternal allele |
yes |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
_1_3_ |
c.-1687_*240{0} |
r.0 |
p.0 |
- |
likely pathogenic (dominant) |
g.(?_92878375)_(94046216_?)del |
- |
92878375_94046216del |
- |
NR2F1_000045 |
1.2Mb deletion |
PubMed: Chen 2016 |
- |
- |
Unknown |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
_1_3_ |
c.-1687_*240{0} |
r.0 |
p.0 |
- |
likely pathogenic (dominant) |
g.(?_92717119)_(93298594_?)del |
- |
hg18 del 92,742,875 to 93,324,350 bp |
- |
NR2F1_000049 |
582 kb deletion incl. FLJ42709, NR2F1, FAM172A, POU5F2, MIR2277 |
PubMed: Al-Kateb 2013 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
_1_3_ |
c.-1687_*240{0} |
r.0 |
p.0 |
- |
likely pathogenic (dominant) |
g.(92593206_92691223)_(92784673_93074143)del |
- |
- |
- |
NR2F1_000050 |
NR2F1 and AK124699 removed, C5ORF21 partially deleted, cryptic 450-460kB deletion near both q15 and 5q33.2 break points |
PubMed: Brown 2009 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
_1_3_ |
c.-1687_*240{0} |
r.0 |
p.0 |
- |
likely pathogenic (dominant) |
g.(?_90566268)_(95580992_?)del |
- |
90566268_95580992del |
- |
NR2F1_000062 |
5Mb deletion |
PubMed: Chen 2016 |
- |
- |
Unknown |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.1A>G |
r.0 |
p.0 |
- |
pathogenic (dominant) |
g.92920730A>G |
- |
- |
- |
NR2F1_000065 |
- |
PubMed: Rech 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.2T>C |
r.0 |
p.0 |
- |
pathogenic (dominant) |
g.92920731T>C |
- |
- |
- |
NR2F1_000048 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.2T>C |
r.0 |
p.0 |
- |
pathogenic (dominant) |
g.92920731T>C |
- |
- |
- |
NR2F1_000048 |
- |
PubMed: Bertacchi 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.2T>C |
r.0 |
p.0 |
- |
pathogenic (dominant) |
g.92920731T>C |
- |
- |
- |
NR2F1_000048 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.2T>C |
r.0 |
p.0 |
- |
pathogenic (dominant) |
g.92920731T>C |
- |
- |
- |
NR2F1_000048 |
- |
PubMed: Rech 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.2T>G |
r.0 |
p.0 |
- |
pathogenic (dominant) |
g.92920731T>G |
- |
- |
- |
NR2F1_000052 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.2T>G |
r.0 |
p.0 |
- |
pathogenic (dominant) |
g.92920731T>G |
- |
- |
- |
NR2F1_000052 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.2_4delinsGGA |
r.0 |
p.0 |
- |
pathogenic (dominant) |
g.92920731_92920733delinsGGA |
- |
c.2_4delTGGinsGGA |
- |
NR2F1_000042 |
Inconsistency between the body of the manuscript (c.2_4delTGGinsGGA, p. 1146) and Table 1 (c.2_4delinsTGG) in the article by Chen et al, Genet Med (2016). Because the mutation named in the table is isosemantic and incompatible with the described protein consequence, the body of the manuscript was considered (c.2_4delTGGinsGGA, renamed according to HGVS nomenclature to c.2_4delinsGGA). |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
?/. |
- |
c.49G>C |
r.(?) |
p.(Gly17Arg) |
- |
VUS |
g.92920778G>C |
g.93585072G>C |
- |
- |
NR2F1_000015 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Nijmegen |
+?/. |
- |
c.51_69dup |
r.(?) |
p.(Asn24Glyfs*379) |
ACMG |
pathogenic |
g.92920780_92920798dup |
g.93585074_93585092dup |
- |
- |
NR2F1_000094 |
- |
- |
- |
- |
Germline/De novo (untested) |
- |
- |
- |
- |
- |
Jinu Han |
?/. |
- |
c.73C>G |
r.(?) |
p.(Pro25Ala) |
- |
VUS |
g.92920802C>G |
g.93585096C>G |
- |
- |
NR2F1_000016 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Nijmegen |
+?/. |
- |
c.78_96del |
r.(?) |
p.(Gln28Alafs*85) |
ACMG |
likely pathogenic (dominant) |
g.92920807_92920825del |
g.93585101_93585119del |
- |
- |
NR2F1_000033 |
ACMG grading: PVS1,PM2 |
- |
- |
- |
Germline |
- |
- |
- |
- |
- |
Andreas Laner |
+?/. |
- |
c.82C>T |
r.(?) |
p.(Gln28*) |
- |
likely pathogenic (dominant) |
g.92920811C>T |
- |
- |
- |
NR2F1_000037 |
- |
PubMed: Bojanek 2019 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.91_93dup |
r.(?) |
p.(Arg31dup) |
ACMG |
likely pathogenic |
g.92920820_92920822dup |
g.93585114_93585116dup |
- |
- |
NR2F1_000100 |
- |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Jinu Han |
+?/. |
- |
c.103_113delinsCGCCGCCGC |
r.(?) |
p.(Gly35Argfs*361) |
- |
likely pathogenic (dominant) |
g.92920832_92920842delinsCGCCGCCGC |
- |
- |
- |
NR2F1_000053 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
?/. |
- |
c.107G>C |
r.(?) |
p.(Gly36Ala) |
- |
VUS |
g.92920836G>C |
g.93585130G>C |
NR2F1(NM_005654.5):c.107G>C (p.G36A) |
- |
NR2F1_000022 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Rotterdam |
+?/. |
- |
c.115G>T |
r.(?) |
p.(Glu39*) |
- |
likely pathogenic (dominant) |
g.92920844G>T |
- |
- |
- |
NR2F1_000054 |
- |
PubMed: Bertacchi 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.192del |
r.(?) |
p.(Gly65Alafs*54) |
- |
likely pathogenic (dominant) |
g.92920921del |
- |
- |
- |
NR2F1_000092 |
- |
- |
- |
- |
Unknown |
? |
- |
- |
- |
- |
Benjamin Billiet |
-?/. |
- |
c.237G>C |
r.(?) |
p.(Gln79His) |
- |
likely benign |
g.92920966G>C |
g.93585260G>C |
NR2F1(NM_005654.6):c.237G>C (p.Q79H) |
- |
NR2F1_000008 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_AMC |
+?/. |
- |
c.237G>C |
r.(?) |
p.(Gln79His) |
- |
likely pathogenic (dominant) |
g.92920966G>C |
- |
- |
- |
NR2F1_000008 |
- |
- |
- |
- |
Germline |
yes |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.237G>C |
r.(?) |
p.(Gln79His) |
- |
likely pathogenic (dominant) |
g.92920966G>C |
- |
- |
- |
NR2F1_000008 |
- |
- |
- |
- |
Unknown |
yes |
- |
- |
- |
- |
Benjamin Billiet |
?/. |
- |
c.253G>T |
r.(?) |
p.(Glu85*) |
- |
likely pathogenic (dominant) |
g.92920982G>T |
- |
- |
- |
NR2F1_000084 |
- |
PubMed: Hobbs 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.256T>C |
r.(?) |
p.(Cys86Arg) |
- |
likely pathogenic (dominant) |
g.92920985T>C |
- |
- |
- |
NR2F1_000067 |
- |
PubMed: Rech 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.257G>T |
r.(?) |
p.(Cys86Phe) |
- |
likely pathogenic (dominant) |
g.92920986G>T |
- |
- |
- |
NR2F1_000039 |
- |
PubMed: Kaiwar 2017 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.262G>A |
r.(?) |
p.(Val88Met) |
- |
likely pathogenic (dominant) |
g.92920991G>A |
- |
- |
- |
NR2F1_000068 |
- |
PubMed: Rech 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.262G>T |
r.(?) |
p.(Val88Leu) |
- |
likely pathogenic |
g.92920991G>T |
- |
- |
- |
NR2F1_000102 |
- |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
MobiDetails |
?/. |
- |
c.284G>T |
r.(?) |
p.(Gly95Val) |
- |
VUS |
g.92921013G>T |
g.93585307G>T |
NR2F1(NM_005654.4):c.284G>T (p.(Gly95Val)) |
- |
NR2F1_000009 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Leiden |
+?/. |
- |
c.284G>T |
r.(?) |
p.(Gly95Val) |
- |
likely pathogenic (dominant) |
g.92921013G>T |
- |
- |
- |
NR2F1_000009 |
- |
PubMed: Rech 2020 |
- |
- |
Unknown |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.286A>G |
r.(?) |
p.(Lys96Glu) |
- |
pathogenic (dominant) |
g.92921015A>G |
- |
- |
- |
NR2F1_000040 |
- |
PubMed: Martin-Hernandez 2019 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.289C>T |
r.(?) |
p.(His97Tyr) |
ACMG |
likely pathogenic (dominant) |
g.92921018C>T |
g.93585312C>T |
- |
- |
NR2F1_000029 |
ACMG grading: PM6,PP3,PS1,PM2 |
- |
- |
- |
Germline |
- |
- |
- |
- |
- |
Andreas Laner |
+?/. |
- |
c.289C>T |
r.(?) |
p.(His97Tyr) |
- |
likely pathogenic (dominant) |
g.92921018C>T |
- |
- |
- |
NR2F1_000029 |
- |
- |
- |
- |
De novo |
- |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.290A>C |
r.(?) |
p.(His97Pro) |
- |
likely pathogenic (dominant) |
g.92921019A>C |
- |
- |
- |
NR2F1_000069 |
- |
PubMed: Rech 2020 |
- |
- |
Unknown |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.291del |
r.(?) |
p.(Tyr98Thrfs*21) |
- |
likely pathogenic (dominant) |
g.92921020del |
- |
291delC (His79Hisfs*22) |
- |
NR2F1_000055 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.292T>C |
r.(?) |
p.(Tyr98His) |
- |
likely pathogenic (dominant) |
g.92921021T>C |
- |
- |
- |
NR2F1_000056 |
- |
PubMed: Bertacchi 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.293A>G |
r.(?) |
p.(Tyr98Cys) |
- |
likely pathogenic (dominant) |
g.92921022A>G |
- |
- |
- |
NR2F1_000070 |
- |
PubMed: Rech 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.311A>G |
r.(?) |
p.(Glu104Gly) |
- |
likely pathogenic (dominant) |
g.92921040A>G |
- |
- |
- |
NR2F1_000071 |
- |
PubMed: Rech 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.313G>A |
r.(?) |
p.(Gly105Ser) |
- |
likely pathogenic (dominant) |
g.92921042G>A |
- |
- |
- |
NR2F1_000034 |
- |
PubMed: Mio 2020 |
- |
- |
De novo |
yes |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.313G>A |
r.(?) |
p.(Gly105Ser) |
- |
likely pathogenic (dominant) |
g.92921042G>A |
- |
- |
- |
NR2F1_000034 |
- |
PubMed: Mio 2020 |
- |
- |
De novo |
yes |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.314G>A |
r.(?) |
p.(Gly105Asp) |
- |
pathogenic |
g.92921043G>A |
g.93585337G>A |
- |
- |
NR2F1_000017 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Nijmegen |
+/. |
- |
c.314G>A |
r.(?) |
p.(Gly105Asp) |
- |
pathogenic (dominant) |
g.92921043G>A |
- |
- |
- |
NR2F1_000017 |
- |
PubMed: Vissers 2017 |
- |
- |
De novo |
- |
- |
- |
- |
- |
Marc Ferre |
+/. |
- |
c.319A>G |
r.(?) |
p.(Lys107Glu) |
- |
pathogenic (dominant) |
g.92921048A>G |
- |
- |
- |
NR2F1_000035 |
- |
PubMed: Starosta 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.319A>G |
r.(?) |
p.(Lys107Glu) |
- |
likely pathogenic |
g.92921048A>G |
- |
- |
- |
NR2F1_000035 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Nijmegen |
?/. |
- |
c.320A>G |
r.(?) |
p.(Lys107Arg) |
- |
VUS |
g.92921049A>G |
g.93585343A>G |
NR2F1(NM_005654.5):c.320A>G (p.K107R) |
- |
NR2F1_000023 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Rotterdam |
+?/. |
- |
c.323G>A |
r.(?) |
p.(Ser108Asn) |
- |
likely pathogenic (dominant) |
g.92921052G>A |
- |
- |
- |
NR2F1_000080 |
- |
- |
- |
- |
Germline |
yes |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.323G>A |
r.(?) |
p.(Ser108Asn) |
- |
likely pathogenic (dominant) |
g.92921052G>A |
- |
- |
- |
NR2F1_000080 |
- |
- |
- |
- |
Unknown |
yes |
- |
- |
- |
- |
Benjamin Billiet |
?/. |
- |
c.323G>C |
r.(?) |
p.(Ser108Thr) |
- |
VUS |
g.92921052G>C |
- |
NR2F1(NM_005654.6):c.323G>C (p.S108T) |
- |
NR2F1_000095 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Groningen |
+?/. |
- |
c.323G>T |
r.(?) |
p.(Ser108Ile) |
- |
likely pathogenic (dominant) |
g.92921052G>T |
- |
- |
- |
NR2F1_000072 |
- |
PubMed: Rech 2020 |
- |
- |
Unknown |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.328_330del |
r.(?) |
p.(Phe110del) |
- |
likely pathogenic (dominant) |
g.92921057_92921059del |
- |
- |
- |
NR2F1_000057 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.328_330del |
r.(?) |
p.(Phe110del) |
- |
likely pathogenic (dominant) |
g.92921057_92921059del |
- |
- |
- |
NR2F1_000057 |
- |
PubMed: Dimassi 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
1 |
c.335G>A |
r.(?) |
p.(Arg112Lys) |
- |
pathogenic (dominant) |
g.92921064G>A |
g.93585358G>A |
- |
- |
NR2F1_000004 |
- |
PubMed: Bosch 2014, Journal: Bosch 2014, OMIM:var0004 |
- |
rs587777277 |
De novo |
- |
- |
- |
- |
- |
Marc Ferre |
+/. |
1 |
c.339C>A |
r.(?) |
p.(Ser113Arg) |
- |
pathogenic (dominant) |
g.92921068C>A |
g.93585362C>A |
- |
- |
NR2F1_000001 |
- |
PubMed: Bosch 2014, Journal: Bosch 2014, OMIM:var0002, PubMed: Bosch 2016, Journal: Bosch 2016 |
- |
rs587777275 |
De novo |
- |
- |
- |
- |
- |
Danielle Bosch |
+/. |
- |
c.339C>A |
r.(?) |
p.(Ser113Arg) |
- |
pathogenic |
g.92921068C>A |
g.93585362C>A |
- |
- |
NR2F1_000001 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Nijmegen |
+/. |
1 |
c.344G>C |
r.(?) |
p.(Arg115Pro) |
- |
pathogenic (dominant) |
g.92921073G>C |
g.93585367G>C |
- |
- |
NR2F1_000002 |
- |
PubMed: Bosch 2014, Journal: Bosch 2014, OMIM:var0001 |
- |
- |
De novo |
- |
- |
- |
- |
- |
Danielle Bosch |
+?/. |
- |
c.365G>C |
r.(?) |
p.(Cys122Ser) |
- |
likely pathogenic (dominant) |
g.92921094G>C |
- |
- |
- |
NR2F1_000073 |
- |
PubMed: Rech 2020 |
- |
- |
Unknown |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.366C>G |
r.(?) |
p.(Cys122Trp) |
- |
likely pathogenic (dominant) |
g.92921095C>G |
- |
- |
- |
NR2F1_000086 |
- |
PubMed: Balciuniene 2019 |
- |
- |
Unknown |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.368G>T |
r.(?) |
p.(Arg123Leu) |
- |
likely pathogenic (dominant) |
g.92921097G>T |
- |
- |
- |
NR2F1_000093 |
- |
- |
- |
- |
Germline/De novo (untested) |
- |
- |
- |
- |
- |
Marc Ferre |
+?/. |
- |
c.380dup |
r.(?) |
p.(Asn127Lysfs*270) |
- |
likely pathogenic (dominant) |
g.92921109dup |
- |
- |
- |
NR2F1_000074 |
- |
PubMed: Rech 2020 |
- |
- |
Unknown |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.382T>C |
r.(?) |
p.(Cys128Arg) |
- |
likely pathogenic (dominant) |
g.92921111T>C |
- |
- |
- |
NR2F1_000041 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.403C>A |
r.(?) |
p.(Arg135Ser) |
- |
likely pathogenic (dominant) |
g.92921132C>A |
- |
- |
- |
NR2F1_000075 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.403C>T |
r.(?) |
p.(Arg135Cys) |
- |
likely pathogenic |
g.92921132C>T |
g.93585426C>T |
- |
- |
NR2F1_000018 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Nijmegen |
+?/. |
- |
c.403C>T |
r.(?) |
p.(Arg135Cys) |
- |
likely pathogenic (dominant) |
g.92921132C>T |
- |
- |
- |
NR2F1_000018 |
- |
PubMed: Hino-Fukuyo 2017 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
?/. |
- |
c.408C>A |
r.(?) |
p.(Asn136Lys) |
- |
VUS |
g.92921137C>A |
- |
NR2F1(NM_005654.5):c.408C>A (p.N136K) |
- |
NR2F1_000098 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Rotterdam |
+/. |
1 |
c.413G>A |
r.(?) |
p.(Cys138Tyr) |
- |
pathogenic (dominant) |
g.92921142G>A |
g.93585436G>A |
- |
- |
NR2F1_000007 |
- |
PubMed: Eldomery 2017, Journal: Eldomery 2017 |
- |
- |
De novo |
- |
- |
- |
- |
- |
Johan den Dunnen |
+?/. |
- |
c.413G>A |
r.(?) |
p.(Cys138Tyr) |
- |
likely pathogenic (dominant) |
g.92921142G>A |
- |
- |
- |
NR2F1_000007 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.417A>T |
r.(?) |
p.(Gln139His) |
- |
likely pathogenic (dominant) |
g.92921146A>T |
- |
- |
- |
NR2F1_000076 |
- |
PubMed: Rech 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.425G>A |
r.(?) |
p.(Arg142His) |
- |
likely pathogenic (dominant) |
g.92921154G>A |
- |
- |
- |
NR2F1_000059 |
- |
PubMed: Bertacchi 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.425G>T |
r.(?) |
p.(Arg142Leu) |
- |
likely pathogenic |
g.92921154G>T |
- |
- |
- |
NR2F1_000058 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
- |
c.436T>C |
r.(?) |
p.(Cys146Arg) |
- |
likely pathogenic |
g.92921165T>C |
g.93585459T>C |
NR2F1(NM_005654.6):c.436T>C (p.C146R) |
- |
NR2F1_000010 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Utrecht |
+?/. |
- |
c.436T>C |
r.(?) |
p.(Cys146Arg) |
- |
likely pathogenic (dominant) |
g.92921165T>C |
- |
- |
- |
NR2F1_000010 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
?/. |
- |
c.452T>C |
r.(?) |
p.(Met151Thr) |
- |
VUS |
g.92921181T>C |
g.93585475T>C |
NR2F1(NM_005654.5):c.452T>C (p.M151T) |
- |
NR2F1_000011 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Rotterdam |
+?/. |
- |
c.463G>A |
r.(?) |
p.(Ala155Thr) |
- |
likely pathogenic |
g.92921192G>A |
g.93585486G>A |
- |
- |
NR2F1_000024 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Nijmegen |
+?/. |
- |
c.463G>A |
r.(?) |
p.(Ala155Thr) |
- |
likely pathogenic (dominant) |
g.92921192G>A |
- |
- |
- |
NR2F1_000024 |
- |
PubMed: Chen 2016 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.513C>A |
r.(?) |
p.(Tyr171Ter) |
- |
pathogenic |
g.92923672C>A |
- |
NR2F1(NM_005654.6):c.513C>A (p.Y171*) |
- |
NR2F1_000012 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_AMC |
+?/. |
- |
c.513C>G |
r.(?) |
p.(Tyr171*) |
- |
likely pathogenic (dominant) |
g.92923672C>G |
- |
- |
- |
NR2F1_000038 |
- |
PubMed: Park 2019 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.513C>G |
r.(?) |
p.(Tyr171*) |
ACMG |
likely pathogenic |
g.92923672C>G |
- |
- |
- |
NR2F1_000038 |
- |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Jinu Han |
+/. |
- |
c.535dup |
r.(?) |
p.(Leu179Profs*218) |
- |
pathogenic |
g.92923694dup |
- |
NR2F1(NM_005654.5):c.535dupC (p.L179Pfs*218) |
- |
NR2F1_000096 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Rotterdam |
?/. |
- |
c.581G>T |
r.(?) |
p.(Arg194Leu) |
- |
VUS |
g.92923740G>T |
- |
NR2F1(NM_005654.6):c.581G>T (p.R194L) |
- |
NR2F1_000097 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Groningen |
+/. |
- |
c.602C>A |
r.(?) |
p.(Ser201*) |
- |
pathogenic (dominant) |
g.92923761C>A |
- |
- |
- |
NR2F1_000085 |
- |
PubMed: Zou 2020 |
- |
- |
De novo |
- |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.603_606del |
r.(?) |
p.(Arg202Thrfs*154) |
- |
pathogenic |
g.92923762_92923765del |
- |
NR2F1(NM_005654.5):c.603_606delGCGC (p.R202Tfs*154) |
- |
NR2F1_000088 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Rotterdam |
-?/. |
- |
c.708C>T |
r.(?) |
p.(Asn236=) |
- |
likely benign |
g.92923867C>T |
g.93588161C>T |
NR2F1(NM_005654.5):c.708C>T (p.N236=) |
- |
NR2F1_000030 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Rotterdam |
+?/. |
- |
c.729_730delinsCT |
r.(?) |
p.(Gln244*) |
- |
likely pathogenic (dominant) |
g.92923888_92923889delinsCT |
- |
- |
- |
NR2F1_000060 |
- |
PubMed: Bertacchi 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
2 |
c.755T>C |
r.(?) |
p.(Leu252Pro) |
- |
pathogenic (dominant) |
g.92923914T>C |
g.93588208T>C |
- |
- |
NR2F1_000003 |
- |
PubMed: Bosch 2014, Journal: Bosch 2014, OMIM:var0003 |
- |
rs587777276 |
De novo |
- |
- |
- |
- |
- |
Marc Ferre |
+/. |
2 |
c.854C>A |
r.(?) |
p.(Ser285*) |
- |
pathogenic (dominant) |
g.92924013C>A |
- |
- |
- |
NR2F1_000090 |
- |
- |
- |
- |
Germline/De novo (untested) |
? |
- |
- |
- |
- |
Marc Ferre |
?/. |
- |
c.883T>C |
r.(?) |
p.(Phe295Leu) |
- |
VUS |
g.92924042T>C |
- |
- |
- |
NR2F1_000081 |
- |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Benjamin Billiet |
?/. |
2 |
c.909G>C |
r.(?) |
p.(Gln303His) |
- |
VUS |
g.92924068G>C |
g.93588362G>C |
- |
- |
NR2F1_000005 |
not associated with disease phneotype |
PubMed: Bosch 2014, Journal: Bosch 2014 |
- |
- |
Germline |
no |
- |
- |
- |
- |
Johan den Dunnen |
+?/. |
- |
c.931G>C |
r.(?) |
p.(Ala311Pro) |
- |
likely pathogenic (dominant) |
g.92924090G>C |
- |
- |
- |
NR2F1_000077 |
- |
PubMed: Rech 2020 |
- |
- |
Unknown |
? |
- |
- |
- |
- |
Benjamin Billiet |
+/. |
- |
c.954G>C |
r.(?) |
p.(Glu318Asp) |
- |
pathogenic |
g.92924113G>C |
g.93588407G>C |
- |
- |
NR2F1_000019 |
VKGL data sharing initiative Nederland |
- |
- |
- |
CLASSIFICATION record |
- |
- |
- |
- |
- |
VKGL-NL_Nijmegen |
+?/. |
- |
c.954G>C |
r.(?) |
p.(Glu318Asp) |
- |
likely pathogenic (dominant) |
g.92924113G>C |
- |
- |
- |
NR2F1_000019 |
- |
PubMed: Rech 2020 |
- |
- |
De novo |
? |
- |
- |
- |
- |
Benjamin Billiet |
+?/. |
2 |
c.965T>A |
r.(?) |
p.(Leu322His) |
- |
likely pathogenic (dominant) |
g.92924124T>A |
- |
- |
- |
NR2F1_000091 |
- |
- |
- |
- |
Germline/De novo (untested) |
? |
- |
- |
- |
- |
Marc Ferre |