Variant #0000002078 (NC_000002.12:g.203867624C>T, NM_005214.4:c.-319C>T (CTLA4))

Individual ID 00000440
Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.203867624C>T
Published as -
Reference Zulkarnain Md Idris et al.(2011)
DB-ID CTLA4_000008
dbSNP ID rs5742909
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-02-21 16:21:06 +08:00 (CST)
Date last edited 2021-08-01 13:01:57 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
CTLA4 NM_005214.4 +/. - c.-319C>T - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000477 DNA PCR CTLA4 6 Nur Aisyah Athirah