Variant #0000016525 (NC_000005.9:g.131722830_131722831del, SLC22A5(NM_003060.3):c.938_939del)

Chromosome 5
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.131722830_131722831del
Reference Shuting Wang et al. (2020)
DB-ID SLC22A5_000064
Frequency 1/667
Variant remarks -
ClassClinical -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner ting zhang
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by ting zhang
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC22A5 NM_003060.3 +?/+? 5 c.938_939del r.0? Phe313*