Variant #0010906379 (NC_000017.10:g.79096082G>A, NM_006340.2:c.*6531G>A (BAIAP2))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.79096082G>A
DB-ID -
dbSNP ID rs577458342
gnomAD frequency 71/97292
gnomAD homozygote count 1/48573
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.1654delCinsT r.(?) p.(Pro552Ser)
BAIAP2 NM_001144888.1 ./. c.*6443G>A r.(=) p.(=)
AATK NM_004920.2 ./. c.1345delCinsT r.(?) p.(Pro449Ser)
BAIAP2 NM_006340.2 ./. c.*6531G>A r.(=) p.(=)
BAIAP2 NM_017451.2 ./. c.*5977G>A r.(=) p.(=)