Variant #0000720401 (NC_000005.9:g.33982369_33982370dup, NM_016180.3:c.533_534dup (SLC45A2))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.33982369_33982370dup
DNA change (hg38) -
Published as SLC45A2(NM_001012509.4):c.533_534dupAG (p.G179Rfs*23)
ISCN -
DB-ID SLC45A2_000025 See all 3 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.*6828_*6829dup r.(=) p.(=)
SLC45A2 NM_016180.3 +/. - c.533_534dup r.(?) p.(Gly179Argfs*23)


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