Variant #0007800929 (NC_000012.11:g.8990098C>T, NM_144670.4:c.791delCinsT (A2ML1))

Chromosome 12
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.8990098C>T
DB-ID -
dbSNP ID rs745514929
gnomAD frequency 1/246244
gnomAD homozygote count 0/123115
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     
A2ML1 NM_144670.4 ./. c.791delCinsT r.(?) p.(Thr264Ile)