Variant #0000804271 (NC_000010.10:g.103534948_103534965dup, NM_033163.3:c.86_103dup (FGF8))

Chromosome 10
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.103534948_103534965dup
DNA change (hg38) -
Published as FGF8(NM_001206389.1):c.-123-321_-123-304dup (p.(=)), FGF8(NM_033163.3):c.86_103dupGCCCTGCGCTGGGCAGGG (p.G29_R34dup), FGF8(NM_033163.4):c.86_103dupG...
ISCN -
DB-ID FGF8_000005 See all 4 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGF8 NM_033163.3 -?/. - c.86_103dup r.(?) p.(Gly29_Arg34dup)


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