Variant #0000990792 (NC_000001.10:g.209849118_209849129del, NM_015714.3:c.89_100del (G0S2))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.209849118_209849129del
DNA change (hg38) -
Published as G0S2(NM_015714.3):c.89_100delGCAGCGTGCTGG (p.(Gly30_Leu33del))
ISCN -
DB-ID G0S2_000002
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
G0S2 NM_015714.3 ?/. - c.89_100del r.(?) p.(Gly30_Leu33del)


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