Variant #0000569246 (NC_000020.10:g.25060079G>T, NM_014588.5:c.496C>A (VSX1))

Chromosome 20
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.25060079G>T
DNA change (hg38) g.25079443G>T
Published as VSX1(NM_001256272.1):c.496C>A (p.R166=)
ISCN -
DB-ID VSX1_000005
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) 3.0E-5 View details
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 2020-07-16 15:15:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
VSX1 NM_001256271.1 -?/. - c.496C>A r.(?) p.(Arg166=)
VSX1 NM_014588.5 -?/. - c.496C>A r.(?) p.(Arg166=)


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