Variant #0000016142 (NC_000005.9:g.131705916_131705929dup14, SLC22A5(NM_003060.3):c.252_265dup14)

Chromosome 5
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type Duplication
DNA change (genomic) (Relative to hg19 / GRCh37) g.131705916_131705929dup14
Reference Xiaole Li et al. (2019)
DB-ID SLC22A5_000015
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC22A5 NM_003060.3 +?/+? 1 c.252_265dup14 r.0? Ile89Thrfs*46