Variant #0013079609 (NC_000023.10:g.152986398A>C, NM_001256447.1:c.122T>G (BCAP31))

Chromosome X
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.152986398A>C
DB-ID -
dbSNP ID rs782741922
gnomAD frequency 145/176679
gnomAD homozygote count 0/121357
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.-4324A>C r.(=) p.(=)
BCAP31 NM_001139441.1 ./. c.122T>G r.(?) p.(Val41Gly)
BCAP31 NM_001139457.2 ./. c.323T>G r.(?) p.(Val108Gly)
BCAP31 NM_001256447.1 ./. c.122T>G r.(?) p.(Val41Gly)
BCAP31 NM_005745.7 ./. c.122T>G r.(?) p.(Val41Gly)