Variant #0000525549 (NC_000005.9:g.33982475C>T, NM_016180.3:c.428G>A (SLC45A2))

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.33982475C>T
DNA change (hg38) g.33982370C>T
Published as SLC45A2(NM_001012509.4):c.428G>A (p.S143N)
ISCN -
DB-ID AMACR_000007
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 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMACR NM_014324.5 ?/. - c.*6723G>A r.(=) p.(=)
SLC45A2 NM_016180.3 ?/. - c.428G>A r.(?) p.(Ser143Asn)


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