Variant #0000259074 (NC_000005.9:g.33989518C>T, NM_016180.3:c.-4830G>A (SLC45A2))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.33989518C>T
DNA change (hg38) g.33989413C>T
Published as AMACR(NM_014324.6):c.829G>A (p.E277K), C1QTNF3-AMACR(NR_037951.1):n.1185G>A
ISCN -
DB-ID AMACR_000003
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) 0.69974 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.829G>A r.(?) p.(Glu277Lys)
SLC45A2 NM_016180.3 -/. - c.-4830G>A r.(?) p.(=)


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