Variant #0000959768 (NC_000001.10:g.120529603C>T, NM_024408.3:c.854G>A (NOTCH2))

Chromosome 1
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.120529603C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID NOTCH2_000160 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs782452794
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-02-06 10:17:01 +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     
NOTCH2 NM_024408.3 ?/. - c.854G>A r.(?) p.(Arg285His)


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