Variant #0000524141 (NC_000005.9:g.131630594C>T, NM_003059.2:c.285C>T (SLC22A4))

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.131630594C>T
DNA change (hg38) g.132294901C>T
Published as SLC22A4(NM_003059.3):c.285C>T (p.L95=)
ISCN -
DB-ID PDLIM4_000002
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) 0.00014 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-17 15:01:29 +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.285C>T r.(?) p.(Leu95=)
PDLIM4 NM_003687.3 -?/. - c.*22672C>T r.(=) p.(=)


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