Variant #0000801877 (NC_000005.9:g.131705800C>T, NM_003060.3:c.136C>T (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.131705800C>T
DNA change (hg38) -
Published as SLC22A5(NM_003060.3):c.136C>T (p.P46S), SLC22A5(NM_003060.4):c.136C>T (p.(Pro46Ser), p.P46S)
ISCN -
DB-ID SLC22A5_000059 See all 8 reported entries
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) 0.00043 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +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.*26272C>T r.(=) p.(=)
SLC22A5 NM_003060.3 +/. - c.136C>T r.(?) p.(Pro46Ser)


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