Variant #0000193887 (NC_000019.9:g.58858719C>T, NM_130786.3:c.1480G>A (A1BG))

Chromosome 19
Allele Both (homozygous)
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.58858719C>T
DNA change (hg38) g.58347353C>T
Published as -
ISCN -
DB-ID A1BG_000005 See all 6 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-09-01 10:33:09 +02:00 (CEST)
Date last edited 2020-07-16 14:19:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
A1BG NM_130786.3 ?/. - c.1480G>A r.(?) p.(Glu494Lys)


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