Variant #0000000097 (NC_000007.14:g.87550285A>G, NM_000927.4:c.1236T>C (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.87550285A>G
Published as -
Reference Haerian BS et al.(2011)dbSNP
DB-ID ABCB1_000003
dbSNP ID rs1128503
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 17:24:41 +08:00 (CST)
Date last edited 2021-09-08 16:09:28 +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     
ABCB1 NM_000927.4 -/. 12 c.1236T>C - r.(=) p.(=) - ClinVar