Variant #0000890643 (NC_000012.11:g.50499364G>C, NM_005276.3:c.253G>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.50499364G>C
DNA change (hg38) -
Published as GPD1(NM_005276.4):c.253G>C (p.D85H)
ISCN -
DB-ID COX14_000094
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 2022-11-01 13:01:21 +01:00 (CET)
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     
SMARCD1 NM_003076.4 ?/. - c.*6581G>C r.(=) p.(=)
GPD1 NM_005276.3 ?/. - c.253G>C r.(?) p.(Asp85His)
COX14 NM_032901.3 ?/. - c.-6729G>C r.(?) p.(=)


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