Variant #0000912317 (NC_000005.9:g.33988484A>G, NM_016180.3:c.-3796T>C (SLC45A2))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.33988484A>G
DNA change (hg38) -
Published as AMACR(NM_014324.6):c.*714T>C
ISCN -
DB-ID AMACR_000014
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) 0.0007 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 2023-01-11 15:44:22 +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.*714T>C r.(=) p.(=)
SLC45A2 NM_016180.3 -?/. - c.-3796T>C r.(?) p.(=)


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