Variant #0000000200 (NC_000006.11:g.135324165A>C, HBS1L(NM_006620.3):c.431-185T>G)

Chromosome 6
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.135324165A>C
Reference Yi S,et al;dbSNP
DB-ID HBS1L_000008
Frequency -
Variant remarks -
ClassClinical uncertain significance
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     
HBS1L NM_006620.3 ./. - c.431-185T>G r.(=) p.(=)