Variant #0000728162 (NC_000022.10:g.38369810C>G, NM_006941.3:c.1093G>C (SOX10))

Chromosome 22
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.38369810C>G
DNA change (hg38) -
Published as SOX10(NM_006941.3):c.1093G>C (p.G365R, p.(Gly365Arg))
ISCN -
DB-ID SOX10_000092 See all 2 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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOX10 NM_006941.3 ?/. - c.1093G>C r.(?) p.(Gly365Arg)
POLR2F NM_021974.3 ?/. - c.*6088C>G r.(=) p.(=)


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