Variant #0000678275 (NC_000008.10:g.11615875C>A, NM_002052.3:c.1220C>A (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.11615875C>A
DNA change (hg38) -
Published as GATA4(NM_002052.3):c.1220C>A (p.(Pro407Gln)), GATA4(NM_002052.4):c.1220C>A (p.P407Q)
ISCN -
DB-ID GATA4_000016 See all 6 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) 0.00053 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GATA4 NM_002052.3 ?/. - c.1220C>A r.(?) p.(Pro407Gln)


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