Variant #0000622435 (NC_000010.10:g.8100330G>T, NM_001002295.1:c.304G>T (GATA3))

Chromosome 10
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.8100330G>T
DNA change (hg38) g.8058367G>T
Published as GATA3(NM_001002295.1):c.304G>T (p.A102S), GATA3(NM_001002295.2):c.304G>T (p.(Ala102Ser))
ISCN -
DB-ID GATA3_000026 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) 1.0E-5 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GATA3 NM_001002295.1 ?/. - c.304G>T r.(?) p.(Ala102Ser)


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