Variant #0000008947 (NC_000012.11:-, MMAB(NM_052845.3):c.556C>T )

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type missense
DNA change (genomic) (Relative to hg19 / GRCh37) -
Reference GenBank
DB-ID MMAB_00003 See all 15 reported entries
Frequency -
Variant remarks Substitution
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Qi Ming
Database submission license No license selected
Created by Qi Ming
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MMAB NM_052845.3 ./. 07 c.556C>T - p.Arg186Trp