Variant #0009719968 (NC_000016.9:g.16315696A>T, NC_000016.9(NM_001171.5):c.37-8T>A (ABCC6))

Chromosome 16
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.16315696A>T
DB-ID -
dbSNP ID rs753858217
gnomAD frequency 1/239434
gnomAD homozygote count 0/119716
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     
ABCC6 NM_001079528.3 ./. c.37-8T>A r.(=) p.(=)
ABCC6 NM_001171.5 ./. c.37-8T>A r.(=) p.(=)