Variant #0000880630 (NC_000004.11:g.89013499T>C, NM_004827.2:c.1855A>G (ABCG2))

Chromosome 4
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.89013499T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID ABCG2_000012
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1433787722
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-10-14 16:46:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCG2 NM_004827.2 ?/. - c.1855A>G r.(?) p.(Ile619Val)


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