Variant #0006567175 (NC_000010.10:g.52610507G>A, NM_001198819.1:c.41C>T (A1CF))

Chromosome 10
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.52610507G>A
DB-ID -
dbSNP ID rs771032953
gnomAD frequency 24/245908
gnomAD homozygote count 0/122930
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
A1CF NM_001198819.1 ./. c.41C>T r.(?) p.(Ala14Val)
A1CF NM_001198820.1 ./. c.41C>T r.(?) p.(Ala14Val)
A1CF NM_138933.2 ./. c.41C>T r.(?) p.(Ala14Val)