Variant #0001078330 (NC_000016.9:g.16184286A>G, NM_004996.3:c.2485A>G (ABCC1))

Chromosome 16
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.16184286A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr16_007653
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2510180292
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 2026-06-02 11:31:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCC1 NM_004996.3 ?/. - c.2485A>G r.(?) p.(Met829Val)


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