Variant #0000002941 (NC_000007.14:g.208920T>C, NM_001348946.2:c.3435T>C (ABCB1))

Individual ID 00000715
Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.208920T>C
Published as -
Reference Zalina Zahari et al.(2018)
DB-ID ABCB1_000007
dbSNP ID rs1045642
Frequency 43.4%
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 15:40:40 +08:00 (CST)
Date last edited 2021-08-01 13:12:21 +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_001348946.2 +/. 26 c.3435T>C - r.(=) p.(=) - Benign



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000807 DNA PCR ABCB1 4 Nur Aisyah Athirah