Variant #0013079636 (NC_000023.10:g.152988634G>A, NM_001256447.1:c.66C>T (BCAP31))

Chromosome X
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.152988634G>A
DB-ID -
dbSNP ID rs782522172
gnomAD frequency 3/178063
gnomAD homozygote count 0/122415
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     
ABCD1 NM_000033.3 ./. c.-2088G>A r.(=) p.(=)
BCAP31 NM_001139441.1 ./. c.66C>T r.(?) p.(Leu22=)
BCAP31 NM_001139457.2 ./. c.267C>T r.(?) p.(Leu89=)
BCAP31 NM_001256447.1 ./. c.66C>T r.(?) p.(Leu22=)
BCAP31 NM_005745.7 ./. c.66C>T r.(?) p.(Leu22=)