Variant #0000194129 (NC_000023.10:g.79269442A>C, NM_001109878.1:c.-947A>C (TBX22))

Chromosome X
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.79269442A>C
DNA change (hg38) g.80013943A>C
Published as -815A>C
ISCN -
DB-ID TBX22_000034 See all 7 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs6523677
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Global Variome, with Curator vacancy
Date created 2011-11-21 23:46:52 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBX22 NM_001109878.1 ?/. 1 c.-947A>C r.(=) p.(=)


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