Variant #0000622918 (NC_000012.11:g.50497834A>G, NM_005276.3:c.1A>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.50497834A>G
DNA change (hg38) g.50104051A>G
Published as GPD1(NM_001257199.1):c.1A>G (p.(Met1?)), GPD1(NM_005276.4):c.1A>G (p.M1?)
ISCN -
DB-ID SMARCD1_000008 See all 2 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) 0.00028 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCD1 NM_003076.4 ?/. - c.*5051A>G r.(=) p.(=)
GPD1 NM_005276.3 ?/. - c.1A>G r.(?) p.(Met1?)


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