Variant #0000000158 (NC_000006.11:g.135442525T>C, MYB(NM_001130173.1):c.-60127T>C)

Chromosome 6
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.135442525T>C
Reference C-C So,et al;dbSNP
DB-ID MYB_000003
Frequency 132/238
Variant remarks -
ClassClinical Likely benign
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     
MYB NM_001130173.1 ./. - c.-60127T>C r.(=) p.(=)