Variant #0010905899 (NC_000017.10:g.79094164G>C, NM_006340.2:c.*4613G>C (BAIAP2))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.79094164G>C
DB-ID -
dbSNP ID rs372185250
gnomAD frequency 1/234280
gnomAD homozygote count 0/117126
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.3572delCinsG r.(?) p.(Ala1191Gly)
BAIAP2 NM_001144888.1 ./. c.*4525G>C r.(=) p.(=)
AATK NM_004920.2 ./. c.3263delCinsG r.(?) p.(Ala1088Gly)
BAIAP2 NM_006340.2 ./. c.*4613G>C r.(=) p.(=)
BAIAP2 NM_017451.2 ./. c.*4059G>C r.(=) p.(=)