Variant #0004958003 (NC_000007.13:g.48319333C>G, NM_152701.3:c.8542delCinsG (ABCA13))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48319333C>G
DB-ID -
dbSNP ID rs766537256
gnomAD frequency 1/245176
gnomAD homozygote count 0/122586
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.8542delCinsG r.(?) p.(Leu2848Val)