Variant #0010491676 (NC_000017.10:g.35306469T>G, NM_012138.3:c.44T>G (AATF))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.35306469T>G
DB-ID -
dbSNP ID rs760414667
gnomAD frequency 7/204340
gnomAD homozygote count 0/102163
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.*6041T>G r.(=) p.(=)
AATF NM_012138.3 ./. c.44T>G r.(?) p.(Leu15Trp)