Variant #0000572017 (NC_000022.10:g.38370180A>T, NM_006941.3:c.723T>A (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.38370180A>T
DNA change (hg38) g.37974173A>T
Published as SOX10(NM_006941.3):c.723T>A (p.P241=)
ISCN -
DB-ID SOX10_000090 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-10-29 08:47:38 +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.723T>A r.(?) p.(Pro241=)
POLR2F NM_021974.3 -?/. - c.*6458A>T r.(=) p.(=)


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