Variant #0009611666 (NC_000016.9:g.2376483G>C, NM_001089.2:c.-16C>G (ABCA3))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.2376483G>C
DB-ID -
dbSNP ID rs375400054
gnomAD frequency 1/228892
gnomAD homozygote count 0/114435
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.-16C>G r.(=) p.(=)