Variant #0007485969 (NC_000011.9:g.77531566T>C, NC_000011.9(NM_016578.3):c.187+8A>G (RSF1))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.77531566T>C
DB-ID -
dbSNP ID rs778818302
gnomAD frequency 1/137320
gnomAD homozygote count 0/68659
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     
RSF1 NM_016578.3 ./. c.187+8A>G r.(=) p.(=)
AAMDC NM_024684.2 ./. c.-740T>C r.(=) p.(=)