Variant #0000321980 (NC_000011.9:g.2946335G>A, NM_183233.2:c.1183G>A (SLC22A18))

Chromosome 11
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.2946335G>A
DNA change (hg38) g.2925105G>A
Published as SLC22A18(NM_002555.5):c.1183G>A (p.(Val395Ile)), SLC22A18(NM_183233.2):c.1183G>A (p.V395I)
ISCN -
DB-ID SLC22A18_000011 See all 2 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) 0.00049 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHLDA2 NM_003311.3 -?/. - c.*3573C>T r.(=) p.(=)
SLC22A18AS NM_007105.2 -?/. - c.-21862C>T r.(?) p.(=)
SLC22A18 NM_183233.2 -?/. - c.1183G>A r.(?) p.(Val395Ile)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.