Variant #0007486002 (NC_000011.9:g.77531767C>T, NM_016578.3:c.-7G>A (RSF1))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.77531767C>T
DB-ID -
dbSNP ID rs576214470
gnomAD frequency 4/138626
gnomAD homozygote count 0/69308
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     
RSF1 NM_016578.3 ./. c.-7G>A r.(=) p.(=)
AAMDC NM_024684.2 ./. c.-539C>T r.(=) p.(=)