Variant #0001006060 (NC_000022.10:g.38370253_38370263del, NC_000022.10(NM_006941.3):c.698-52_698-42del (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.38370253_38370263del
DNA change (hg38) -
Published as SOX10(NM_006941.3):c.698-52_698-42delCTCTAACCTGC (p.?)
ISCN -
DB-ID POLR2F_000023 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 2024-08-28 13:16:32 +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.698-52_698-42del r.(=) p.(=)
POLR2F NM_021974.3 +/. - c.*6531_*6541del r.(=) p.(=)


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