Variant #0001014989 (NC_000012.11:g.50499348_50499350del, NM_005276.3:c.237_239del (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.50499348_50499350del
DNA change (hg38) -
Published as GPD1(NM_005276.4):c.237_239delGGT (p.V80del)
ISCN -
DB-ID COX14_000118
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 2024-10-29 21:08:56 +01:00 (CET)
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.*6565_*6567del r.(=) p.(=)
GPD1 NM_005276.3 ?/. - c.237_239del r.(?) p.(Val80del)
COX14 NM_032901.3 ?/. - c.-6745_-6743del r.(?) p.(=)


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