Variant #0000609461 (NC_000005.9:g.131649405T>A, NM_003060.3:c.-56260T>A (SLC22A5))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.131649405T>A
DNA change (hg38) g.132313712T>A
Published as SLC22A4(NM_003059.3):c.596T>A (p.L199*)
ISCN -
DB-ID SLC22A4_000005
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00011 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-17 15:01:43 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC22A4 NM_003059.2 +/. - c.596T>A r.(?) p.(Leu199Ter)
SLC22A5 NM_003060.3 +/. - c.-56260T>A r.(?) p.(=)


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