Variant #0007800563 (NC_000012.11:g.8975783A>G, NM_144670.4:c.68A>G (A2ML1))

Chromosome 12
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.8975783A>G
DB-ID -
dbSNP ID rs750524549
gnomAD frequency 11/244986
gnomAD homozygote count 1/122483
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.68A>G r.(?) p.(Tyr23Cys)