Variant #0000657856 (NC_000016.9:g.48249113A>G, NM_032583.3:c.1094T>C (ABCC11))

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.48249113A>G
DNA change (hg38) g.48215202A>G
Published as ABCC11(NM_033151.3):c.1094T>C (p.I365T)
ISCN -
DB-ID ABCC11_000007
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LONP2 NM_031490.2 ?/. - c.-29187A>G r.(?) p.(=)
ABCC11 NM_032583.3 ?/. - c.1094T>C r.(?) p.(Ile365Thr)


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