Variant #0013079598 (NC_000023.10:g.152986313C>T, NC_000023.10(NM_001256447.1):c.193+14G>A (BCAP31))

Chromosome X
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.152986313C>T
DB-ID -
dbSNP ID -
gnomAD frequency 1/177089
gnomAD homozygote count 0/121431
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.-4409C>T r.(=) p.(=)
BCAP31 NM_001139441.1 ./. c.193+14G>A r.(=) p.(=)
BCAP31 NM_001139457.2 ./. c.394+14G>A r.(=) p.(=)
BCAP31 NM_001256447.1 ./. c.193+14G>A r.(=) p.(=)
BCAP31 NM_005745.7 ./. c.193+14G>A r.(=) p.(=)