Variant #0000298436 (NC_000022.10:g.38379388C>G, NM_006941.3:c.404G>C (SOX10))

Chromosome 22
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.38379388C>G
DNA change (hg38) g.37983381C>G
Published as SOX10(NM_006941.4):c.404G>C (p.S135T)
ISCN -
DB-ID SOX10_000007 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
SOX10 NM_006941.3 +/. 2 c.404G>C r.(?) p.(Ser135Thr)
POLR2F NM_021974.3 +/. - c.*15666C>G r.(=) p.(=)


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