Variant #0000913872 (NC_000012.11:g.50499344A>C, NM_005276.3:c.233A>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.50499344A>C
DNA change (hg38) -
Published as GPD1(NM_005276.4):c.233A>C (p.D78A)
ISCN -
DB-ID COX14_000102
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCD1 NM_003076.4 ?/. - c.*6561A>C r.(=) p.(=)
GPD1 NM_005276.3 ?/. - c.233A>C r.(?) p.(Asp78Ala)
COX14 NM_032901.3 ?/. - c.-6749A>C r.(?) p.(=)


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