Variant #0010905644 (NC_000017.10:g.79092169C>T, NM_006340.2:c.*2618C>T (BAIAP2))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.79092169C>T
DB-ID -
dbSNP ID rs369140728
gnomAD frequency 8/210938
gnomAD homozygote count 0/105460
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     
AATK NM_001080395.2 ./. c.*33delGinsA r.(=) p.(=)
BAIAP2 NM_001144888.1 ./. c.*2530C>T r.(=) p.(=)
AATK NM_004920.2 ./. c.*33delGinsA r.(=) p.(=)
BAIAP2 NM_006340.2 ./. c.*2618C>T r.(=) p.(=)
BAIAP2 NM_017451.2 ./. c.*2064C>T r.(=) p.(=)