Variant #0007486004 (NC_000011.9:g.77531775_77531776insGGA, NM_016578.3:c.-16_-15insTCC (RSF1))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.77531775_77531776insGGA
DB-ID -
dbSNP ID -
gnomAD frequency 2/135658
gnomAD homozygote count 0/67827
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.-16_-15insTCC r.(=) p.(=)
AAMDC NM_024684.2 ./. c.-531_-530insGGA r.(=) p.(=)