Variant #0000609592 (NC_000005.9:g.150407593A>G, NM_001252385.1:c.*2749T>C (TNIP1))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.150407593A>G
DNA change (hg38) g.151028032A>G
Published as GPX3(NM_002084.3):c.583A>G (p.(Ile195Val))
ISCN -
DB-ID GPX3_000002
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-18 09:04:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNIP1 NM_001252385.1 ?/. - c.*2749T>C r.(=) p.(=)
GPX3 NM_002084.3 ?/. - c.583A>G r.(?) p.?


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