Variant #0009677557 (NC_000016.9:g.8816703G>T, NC_000016.9(NM_000663.4):c.-42+8981G>T (ABAT))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.8816703G>T
DB-ID -
dbSNP ID -
gnomAD frequency 1/123152
gnomAD homozygote count 0/61573
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+8981G>T r.(=) p.(=)
ABAT NM_001127448.1 ./. c.-42+1912G>T r.(=) p.(=)
ABAT NM_020686.5 ./. c.-41-12853G>T r.(=) p.(=)