Variant #0007800555 (NC_000012.11:g.8975748T>C, NC_000012.11(NM_144670.4):c.63-30T>C (A2ML1))

Chromosome 12
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.8975748T>C
DB-ID -
dbSNP ID rs779171627
gnomAD frequency 2/238836
gnomAD homozygote count 0/119416
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.63-30T>C r.(=) p.(=)