Variant #0000339939 (NC_000022.10:g.38369976A>G, NM_006941.3:c.927T>C (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.38369976A>G
DNA change (hg38) g.37973969A>G
Published as POLR2F(NM_001301130.2):c.293+6799A>G, SOX10(NM_006941.3):c.927T>C (p.H309=), SOX10(NM_006941.4):c.927T>C (p.H309=)
ISCN -
DB-ID SOX10_000094 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) 0.64884 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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 -/. 4 c.927T>C r.(?) p.(His309=)
POLR2F NM_021974.3 -/. - c.*6254A>G r.(=) p.(=)


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