Variant #0004851148 (NC_000007.13:g.20685511C>T, NM_001163941.1:c.803+8delCinsT (ABCB5))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.20685511C>T
DB-ID -
dbSNP ID rs745631755
gnomAD frequency 1/244444
gnomAD homozygote count 0/122216
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     
ABCB5 NM_001163941.1 ./. c.803+8delCinsT r.(=) p.(=)
ABCB5 NM_001163942.1 ./. c.-2001C>T r.(=) p.(=)
ABCB5 NM_001163993.1 ./. c.-2001C>T r.(=) p.(=)
ABCB5 NM_178559.5 ./. c.-2001C>T r.(=) p.(=)