Variant #0000000075 (NC_000007.14:g.87509329A>G, NM_000927.4:c.3435T>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.87509329A>G
Published as -
Reference Haerian BS et al.(2011)dbSNP
DB-ID ABCB1_000001
dbSNP ID rs1045642
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 08:27:37 +08:00 (CST)
Date last edited 2021-09-08 16:03:41 +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 ?/. 27 c.3435T>C - r.(=) p.(=) - ClinVar