Variant #0000332494 (NC_000008.10:g.145742850T>C, NM_004260.3:c.161A>G (RECQL4))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.145742850T>C
DNA change (hg38) g.144517466T>C
Published as RECQL4(NM_004260.3):c.161A>G (p.Q54R, p.(Gln54Arg)), RECQL4(NM_004260.4):c.161A>G (p.Q54R)
ISCN -
DB-ID RECQL4_000045 See all 5 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00365 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C8orf82 NM_001001795.1 -?/. - c.*9876A>G r.(=) p.(=)
LRRC24 NM_001024678.3 -?/. - c.*5009A>G r.(=) p.(=)
RECQL4 NM_004260.3 -?/. - c.161A>G r.(?) p.(Gln54Arg)
LRRC14 NM_014665.3 -?/. - c.-687T>C r.(?) p.(=)


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