Variant #0010905980 (NC_000017.10:g.79094637C>G, NM_006340.2:c.*5086C>G (BAIAP2))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.79094637C>G
DB-ID -
dbSNP ID rs372026732
gnomAD frequency 4/183812
gnomAD homozygote count 0/91889
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.3099delGinsC r.(?) p.(Pro1033=)
BAIAP2 NM_001144888.1 ./. c.*4998C>G r.(=) p.(=)
AATK NM_004920.2 ./. c.2790delGinsC r.(?) p.(Pro930=)
BAIAP2 NM_006340.2 ./. c.*5086C>G r.(=) p.(=)
BAIAP2 NM_017451.2 ./. c.*4532C>G r.(=) p.(=)