Variant #0000720402 (NC_000005.9:g.33989506C>G, NM_016180.3:c.-4818G>C (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.33989506C>G
DNA change (hg38) -
Published as AMACR(NM_014324.5):c.841G>C (p.A281P)
ISCN -
DB-ID AMACR_000011
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) 1.0E-5 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMACR NM_014324.5 ?/. - c.841G>C r.(?) p.(Ala281Pro)
SLC45A2 NM_016180.3 ?/. - c.-4818G>C r.(?) p.(=)


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