Variant #0000002908 (NC_000003.12:g.53303G>A, NM_001206924.2:c.217G>A (CD86))

Individual ID 00000713
Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.53303G>A
Published as -
Reference Adiratna Mat Ripen et al.(2020)
DB-ID CD86_000001 See all 2 reported entries
dbSNP ID rs2681417
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 2021-06-27 11:53:36 +08:00 (CST)
Date last edited 2021-08-01 13:11:55 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
CD86 NM_001206924.2 -/. 3 c.217G>A - r.(?) p.(Val73Ile) Benign



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000790 DNA PCR;SEQ CD86 1 Nur Aisyah Athirah