Variant #0000959781 (NC_000001.10:g.120460308G>A, NM_024408.3:c.6007C>T (NOTCH2))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.120460308G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID NOTCH2_000081 See all 3 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs312262801
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-02-06 14:05:01 +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.6007C>T r.(?) p.(Arg2003Ter)


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