Variant #0000925649 (NC_000012.11:g.50501505T>G, NM_005276.3:c.768T>G (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.50501505T>G
DNA change (hg38) -
Published as GPD1(NM_001257199.1):c.699T>G (p.(Cys233Trp)), GPD1(NM_005276.4):c.768T>G (p.C256W)
ISCN -
DB-ID COX14_000005 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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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     
GPD1 NM_005276.3 ?/. - c.768T>G r.(?) p.(Cys256Trp)
COX14 NM_032901.3 ?/. - c.-4588T>G r.(?) p.(=)


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