Variant #0001021175 (NC_000015.9:g.76673763G>A, NM_020843.2:c.3661C>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.76673763G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID SCAPER_000076
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1297546100
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-01-20 16:00:02 +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     
SCAPER NM_020843.2 ?/. - c.3661C>T r.(?) p.(Arg1221Cys)


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