Variant #0004956660 (NC_000007.13:g.48312259T>C, NM_152701.3:c.2996delTinsC (ABCA13))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48312259T>C
DB-ID -
dbSNP ID rs201035977
gnomAD frequency 7/242876
gnomAD homozygote count 0/121430
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     
ABCA13 NM_152701.3 ./. c.2996delTinsC r.(?) p.(Ile999Thr)