Variant #0000283347 (NC_000003.11:g.128204960G>C, NM_001145661.1:c.481C>G (GATA2))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.128204960G>C
DNA change (hg38) g.128486117G>C
Published as GATA2(NM_001145661.1):c.481C>G (p.P161A), GATA2(NM_001145661.2):c.481C>G (p.P161A), GATA2(NM_032638.4):c.481C>G (p.P161A), GATA2(NM_032638.5):c.481...
ISCN -
DB-ID GATA2_000039 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) 0.0082 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GATA2 NM_001145661.1 -/. - c.481C>G r.(?) p.(Pro161Ala)


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