Variant #0000654791 (NC_000003.11:g.128204877C>G, NM_001145661.1:c.564G>C (GATA2))

Chromosome 3
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.128204877C>G
DNA change (hg38) g.128486034C>G
Published as GATA2(NM_001145661.1):c.564G>C (p.(Thr188=), p.T188=), GATA2(NM_001145661.2):c.564G>C (p.T188=)
ISCN -
DB-ID GATA2_000037 See all 4 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) 0.04108 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 2020-03-23 16:13:27 +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     
GATA2 NM_001145661.1 -?/. - c.564G>C r.(?) p.(Thr188=)


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