Variant #0000502788 (NC_000001.10:g.120572547T>C, NM_024408.3:c.137A>G (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.120572547T>C
DNA change (hg38) g.120029924T>C
Published as NOTCH2(NM_024408.3):c.137A>G (p.N46S), NOTCH2(NM_024408.4):c.137A>G (p.N46S)
ISCN -
DB-ID NOTCH2_000121 See all 3 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.137A>G r.(?) p.(Asn46Ser)


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