Variant #0000572018 (NC_000022.10:g.38370233_38370234dup, NC_000022.10(NM_006941.3):c.698-19_698-18dup (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.38370233_38370234dup
DNA change (hg38) g.37974226_37974227dup
Published as SOX10(NM_006941.4):c.698-19_698-18dupCT
ISCN -
DB-ID SOX10_000112
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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 -?/. 3i c.698-19_698-18dup r.(=) p.(=)
POLR2F NM_021974.3 -?/. - c.*6511_*6512dup r.(=) p.(=)


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