Variant #0000980334 (NC_000012.11:g.50497873T>C, NM_005276.3:c.40T>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.50497873T>C
DNA change (hg38) -
Published as GPD1(NM_005276.4):c.40T>C (p.W14R)
ISCN -
DB-ID SMARCD1_000028
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCD1 NM_003076.4 ?/. - c.*5090T>C r.(=) p.(=)
GPD1 NM_005276.3 ?/. - c.40T>C r.(?) p.(Trp14Arg)


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