Variant #0000929410 (NC_000008.10:g.11607694G>A, NM_002052.3:c.858G>A (GATA4))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11607694G>A
DNA change (hg38) -
Published as GATA4(NM_001308093.1):c.861G>A (p.(Ala287=)), GATA4(NM_002052.4):c.858G>A (p.A286=)
ISCN -
DB-ID GATA4_000007 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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +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.858G>A r.(?) p.(Ala286=)


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