Variant #0010491678 (NC_000017.10:g.35306497_35306498insGAAGCGGACCCC, NM_012138.3:c.72_73insGAAGCGGACCCC (AATF))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.35306497_35306498insGAAGCGGACCCC
DB-ID -
dbSNP ID rs764192030
gnomAD frequency 3/203730
gnomAD homozygote count 0/101862
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     
LHX1 NM_005568.3 ./. c.*6069_*6070insGAAGCGGACCCC r.(=) p.(=)
AATF NM_012138.3 ./. c.72_73insGAAGCGGACCCC r.(?) p.(Ala26_Glu29dup)