Variant #0000723193 (NC_000011.9:g.111930670G>T, NM_001931.4:c.1558G>T (DLAT))

Chromosome 11
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.111930670G>T
DNA change (hg38) -
Published as DLAT(NM_001931.5):c.1558G>T (p.G520*)
ISCN -
DB-ID DLAT_000021
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +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     
DLAT NM_001931.4 ?/. - c.1558G>T r.(?) p.(Gly520Ter)
PIH1D2 NM_138789.3 ?/. - c.*7925C>A r.(=) p.(=)


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