Variant #0012964503 (NC_000023.10:g.74332805A>G, NM_004299.4:c.252T>C (ABCB7))

Chromosome X
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74332805A>G
DB-ID -
dbSNP ID rs777100195
gnomAD frequency 18/178075
gnomAD homozygote count 0/122474
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     
ABCB7 NM_001271696.1 ./. c.249T>C r.(?) p.(Ala83=)
ABCB7 NM_001271697.1 ./. c.249T>C r.(?) p.(Ala83=)
ABCB7 NM_001271698.1 ./. c.171T>C r.(?) p.(Ala57=)
ABCB7 NM_001271699.1 ./. c.252T>C r.(?) p.(Ala84=)
ABCB7 NM_004299.4 ./. c.252T>C r.(?) p.(Ala84=)