Variant #0010905431 (NC_000017.10:g.79084697C>G, NM_006340.2:c.1536-17delCinsG (BAIAP2))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.79084697C>G
DB-ID -
dbSNP ID rs373033158
gnomAD frequency 5/246198
gnomAD homozygote count 0/123092
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     
BAIAP2 NM_006340.2 ./. c.1536-17delCinsG r.(=) p.(=)
BAIAP2 NM_017450.2 ./. c.*1899C>G r.(=) p.(=)
AATK XM_005257847.1 ./. c.*4433delGinsC r.(=) p.(=)
AATK XM_005257848.1 ./. c.*4250delGinsC r.(=) p.(=)
AATK XM_005257849.1 ./. c.*4438delGinsC r.(=) p.(=)
AATK XM_005257850.1 ./. c.*4438delGinsC r.(=) p.(=)
AATK XM_005257851.1 ./. c.*4438delGinsC r.(=) p.(=)
AATK XM_005257852.1 ./. c.*4438delGinsC r.(=) p.(=)
AATK XM_005257853.1 ./. c.*4438delGinsC r.(=) p.(=)
AATK XM_005257854.1 ./. c.*4438delGinsC r.(=) p.(=)
AATK XM_005257856.1 ./. c.*5552delGinsC r.(=) p.(=)
AATK XM_005257857.1 ./. c.*5552delGinsC r.(=) p.(=)