Variant #0000984228 (NC_000022.10:g.38379688_38379690dup, NM_006941.3:c.114_116dup (SOX10))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.38379688_38379690dup
DNA change (hg38) -
Published as SOX10(NM_006941.3):c.114_116dupCGG (p.G39dup), SOX10(NM_006941.4):c.114_116dup (p.(Gly39dup))
ISCN -
DB-ID SOX10_000118 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
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.114_116dup r.(?) p.(Gly39dup)
POLR2F NM_021974.3 -?/. - c.*15966_*15968dup r.(=) p.(=)


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