Variant #0000850763 (NC_000005.9:g.131657904G>A, NM_003060.3:c.-47761G>A (SLC22A5))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.131657904G>A
DNA change (hg38) -
Published as SLC22A4(NM_003059.3):c.680G>A (p.R227H)
ISCN -
DB-ID SLC22A4_000010
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) 0.00054 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.680G>A r.(?) p.(Arg227His)
SLC22A5 NM_003060.3 ?/. - c.-47761G>A r.(?) p.(=)


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