Variant #0000693192 (NC_000022.10:g.38379459G>T, NM_006941.3:c.333C>A (SOX10))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.38379459G>T
DNA change (hg38) -
Published as SOX10(NM_006941.3):c.333C>A (p.F111L)
ISCN -
DB-ID SOX10_000128
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2020-10-29 08:47:38 +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.333C>A r.(?) p.(Phe111Leu)
POLR2F NM_021974.3 +?/. - c.*15737G>T r.(=) p.(=)


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