Variant #0013079638 (NC_000023.10:g.152988644A>G, NM_001256447.1:c.56T>C (BCAP31))

Chromosome X
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.152988644A>G
DB-ID -
dbSNP ID -
gnomAD frequency 1/178024
gnomAD homozygote count 0/122376
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.-2078A>G r.(=) p.(=)
BCAP31 NM_001139441.1 ./. c.56T>C r.(?) p.(Val19Ala)
BCAP31 NM_001139457.2 ./. c.257T>C r.(?) p.(Val86Ala)
BCAP31 NM_001256447.1 ./. c.56T>C r.(?) p.(Val19Ala)
BCAP31 NM_005745.7 ./. c.56T>C r.(?) p.(Val19Ala)