Variant #0010905440 (NC_000017.10:g.79084715G>A, NM_006340.2:c.1537G>A (BAIAP2))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.79084715G>A
DB-ID -
dbSNP ID rs145033094
gnomAD frequency 23/246218
gnomAD homozygote count 0/123086
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BAIAP2 NM_006340.2 ./. c.1537G>A r.(?) p.(Ala513Thr)
BAIAP2 NM_017450.2 ./. c.*1917G>A r.(=) p.(=)
AATK XM_005257847.1 ./. c.*4415C>T r.(=) p.(=)
AATK XM_005257848.1 ./. c.*4232C>T r.(=) p.(=)
AATK XM_005257849.1 ./. c.*4420C>T r.(=) p.(=)
AATK XM_005257850.1 ./. c.*4420C>T r.(=) p.(=)
AATK XM_005257851.1 ./. c.*4420C>T r.(=) p.(=)
AATK XM_005257852.1 ./. c.*4420C>T r.(=) p.(=)
AATK XM_005257853.1 ./. c.*4420C>T r.(=) p.(=)
AATK XM_005257854.1 ./. c.*4420C>T r.(=) p.(=)
AATK XM_005257856.1 ./. c.*5534C>T r.(=) p.(=)
AATK XM_005257857.1 ./. c.*5534C>T r.(=) p.(=)