Variant #0012964539 (NC_000023.10:g.74375901T>C, NC_000023.10(NM_004299.4):c.168+39A>G (ABCB7))

Chromosome X
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74375901T>C
DB-ID -
dbSNP ID rs758666998
gnomAD frequency 1/162176
gnomAD homozygote count 0/107819
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.168+39A>G r.(=) p.(=)
ABCB7 NM_001271697.1 ./. c.168+39A>G r.(=) p.(=)
ABCB7 NM_001271698.1 ./. c.168+39A>G r.(=) p.(=)
ABCB7 NM_001271699.1 ./. c.168+39A>G r.(=) p.(=)
ABCB7 NM_004299.4 ./. c.168+39A>G r.(=) p.(=)