Variant #0000533594 (NC_000008.10:g.11607693C>T, NM_002052.3:c.857C>T (GATA4))

Chromosome 8
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.11607693C>T
DNA change (hg38) g.11750184C>T
Published as GATA4(NM_002052.3):c.857C>T (p.(Ala286Val)), GATA4(NM_002052.4):c.857C>T (p.A286V), GATA4(NM_002052.5):c.857C>T (p.A286V)
ISCN -
DB-ID GATA4_000043 See all 3 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) 4.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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     
GATA4 NM_002052.3 ?/. - c.857C>T r.(?) p.(Ala286Val)


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