Variant #0009611678 (NC_000016.9:g.2376519T>C, NC_000016.9(NM_001089.2):c.-26-26A>G (ABCA3))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.2376519T>C
DB-ID -
dbSNP ID -
gnomAD frequency 1/187230
gnomAD homozygote count 0/93614
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCA3 NM_001089.2 ./. c.-26-26A>G r.(=) p.(=)