Variant #0009677520 (NC_000016.9:g.8807732A>C, NC_000016.9(NM_000663.4):c.-42+10A>C (ABAT))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.8807732A>C
DB-ID -
dbSNP ID rs575906448
gnomAD frequency 1/125726
gnomAD homozygote count 0/62862
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABAT NM_000663.4 ./. c.-42+10A>C r.(=) p.(=)
ABAT NM_020686.5 ./. c.-41-21824A>C r.(=) p.(=)