Variant #0000258844 (NC_000016.9:g.48258198C>T, NM_032583.3:c.538G>A (ABCC11))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.48258198C>T
DNA change (hg38) g.48224287C>T
Published as ABCC11(NM_033151.4):c.538G>A (p.G180R)
ISCN -
DB-ID ABCC11_000001 See all 108 reported entries
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) 0.22343 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LONP2 NM_031490.2 -/. - c.-20102C>T r.(?) p.(=)
ABCC11 NM_032583.3 -/. - c.538G>A r.(?) p.(Gly180Arg)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.