Variant #0000548438 (NC_000012.11:g.50500678T>C, NM_005276.3:c.590T>C (GPD1))

Chromosome 12
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.50500678T>C
DNA change (hg38) g.50106895T>C
Published as GPD1(NM_005276.3):c.590T>C (p.V197A), GPD1(NM_005276.4):c.590T>C (p.V197A)
ISCN -
DB-ID COX14_000004 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) 0.00075 View details
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     
GPD1 NM_005276.3 ?/. - c.590T>C r.(?) p.(Val197Ala)
COX14 NM_032901.3 ?/. - c.-5415T>C r.(?) p.(=)


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