Variant #0000850765 (NC_000005.9:g.131676250C>T, NM_003060.3:c.-29415C>T (SLC22A5))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.131676250C>T
DNA change (hg38) -
Published as SLC22A4(NM_003059.3):c.1445-8C>T
ISCN -
DB-ID SLC22A4_000012
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) 0.00035 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 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC22A4 NM_003059.2 -?/. - c.1445-8C>T r.(=) p.(=)
SLC22A5 NM_003060.3 -?/. - c.-29415C>T r.(?) p.(=)


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