Variant #0000927266 (NC_000023.10:g.139586494T>G, NM_005634.2:c.732A>C (SOX3))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.139586494T>G
DNA change (hg38) -
Published as SOX3(NM_005634.2):c.732A>C (p.A244=), SOX3(NM_005634.3):c.732A>C (p.A244=)
ISCN -
DB-ID SOX3_000013 See all 3 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) 0.0164 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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     
SOX3 NM_005634.2 -/. - c.732A>C r.(?) p.(Ala244=)


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