Variant #0000886807 (NC_000005.9:g.33989510C>T, NM_016180.3:c.-4822G>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.33989510C>T
DNA change (hg38) -
Published as AMACR(NM_014324.5):c.837G>A (p.T279=), AMACR(NM_014324.6):c.837G>A (p.T279=)
ISCN -
DB-ID AMACR_000009 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) 0.00124 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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.837G>A r.(?) p.(Thr279=)
SLC45A2 NM_016180.3 -/. - c.-4822G>A r.(?) p.(=)


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