Variant #0000296535 (NC_000001.10:g.120612006G>A, NM_024408.3:c.15C>T (NOTCH2))

Chromosome 1
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.120612006G>A
DNA change (hg38) g.120069392G>A
Published as NOTCH2(NM_024408.3):c.15C>T (p.R5=), NOTCH2(NM_024408.4):c.15C>T (p.R5=, p.(Arg5=))
ISCN -
DB-ID NOTCH2_000060 See all 4 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOTCH2 NM_024408.3 -/. - c.15C>T r.(?) p.(Arg5=)


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