Variant #0000001377 (NC_000012.12:g.57096317T>C, NM_003153.4:c.*255A>G (STAT6))

Individual ID 00000287
Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.57096317T>C
Published as -
Reference Kek Heng Chua et al. (2016), dbSNP
DB-ID STAT6_000001 See all 6 reported entries
dbSNP ID rs324015
Frequency 15/27
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2020-12-21 11:38:36 +08:00 (CST)
Date last edited 2021-08-29 15:37:49 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
STAT6 NM_003153.4 +/. - c.*255A>G - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000302 DNA PCR STAT6 2 Nuur Athirah Binti Mohd Daud