Variant #0000614215 (NC_000012.11:g.50498405_50498406insTTTGTCTACCCAATAAAGCGTGTTTTTTC, NM_005276.3:c.90_91insTTTGTCTACCCAATAAAGCGTGTTTTTTC (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.50498405_50498406insTTTGTCTACCCAATAAAGCGTGTTTTTTC
DNA change (hg38) g.50104622_50104623insTTTGTCTACCCAATAAAGCGTGTTTTTTC
Published as GPD1(NM_001257199.1):c.90_91insTTTGTCTACCCAATAAAGCGTGTTTTTTC (p.?)
ISCN -
DB-ID SMARCD1_000014
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-02 15:24:14 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMARCD1 NM_003076.4 ?/. - c.*5622_*5623insTTTGTCTACCCAATAAAGCGTGTTTTTTC r.(=) p.(=)
GPD1 NM_005276.3 ?/. - c.90_91insTTTGTCTACCCAATAAAGCGTGTTTTTTC r.(?) p.(Gln31PhefsTer16)


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