Variant #0000000096 (NC_000007.14:g.87531302A>C, NM_000927.4:c.2677T>G (ABCB1))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.87531302A>C
Published as -
Reference Haerian BS et al.(2011)dbSNP
DB-ID ABCB1_000002
dbSNP ID rs2032582
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MyHVP
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
Date created 2017-11-21 17:22:21 +08:00 (CST)
Date last edited 2021-09-08 16:07:56 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
ABCB1 NM_000927.4 ?/. 21 c.2677T>G - r.(?) p.(Ser893Ala) - ClinVar