Variant #0000295925 (NC_000005.9:g.33984425del, NM_016180.3:c.264del (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.33984425del
DNA change (hg38) g.33984320del
Published as SLC45A2(NM_001012509.4):c.264delC (p.G89Dfs*24)
ISCN -
DB-ID SLC45A2_000012 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) 9.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-17 09:58:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AMACR NM_014324.5 +/. - c.*4773del r.(?) p.(=)
SLC45A2 NM_016180.3 +/. - c.264del r.(?) p.(Gly89AspfsTer24)


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