Variant #0001075658 (NC_000016.9:g.16200615_16200617del, NM_004996.3:c.2756_2758del (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.16200615_16200617del
DNA change (hg38) -
Published as -
ISCN -
DB-ID ABCC1_000030
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs773097397
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 2026-04-28 15:20:08 +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.2756_2758del r.(?) p.(Ser919del)


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