Variant #0000000192 (NC_000006.11:g.135427817G>A, HBS1L(NM_006620.3):c.-51988C>T)

Chromosome 6
Allele Parent #1
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type Substitution
DNA change (genomic) (Relative to hg19 / GRCh37) g.135427817G>A
Reference C-C So,et al;dbSNP
DB-ID HBS1L_000006 See all 3 reported entries
Frequency 99/238
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HBS1L NM_006620.3 ./. - c.-51988C>T r.(=) p.(=)