Variant #0000970488 (NC_000022.10:g.38379670C>A, NM_006941.3:c.122G>T (SOX10))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38379670C>A
DNA change (hg38) -
Published as SOX10(NM_006941.3):c.122G>T (p.G41V, p.(Gly41Val)), SOX10(NM_006941.4):c.122G>T (p.G41V)
ISCN -
DB-ID SOX10_000101 See all 3 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) 0.00055 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOX10 NM_006941.3 -/. - c.122G>T r.(?) p.(Gly41Val)
POLR2F NM_021974.3 -/. - c.*15948C>A r.(=) p.(=)


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