Variant #0000854183 (NC_000015.9:g.76914159T>A, NM_020843.2:c.2657A>T (SCAPER))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.76914159T>A
DNA change (hg38) -
Published as SCAPER(NM_001353009.1):c.2675A>T (p.Y892F), SCAPER(NM_001353009.2):c.2675A>T (p.Y892F)
ISCN -
DB-ID SCAPER_000049 See all 2 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) 0.00385 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SCAPER NM_020843.2 ?/. - c.2657A>T r.(?) p.(Tyr886Phe)


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