Variant #0000537449 (NC_000009.11:g.139412639G>A, NM_017617.3:c.1205C>T (NOTCH1))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.139412639G>A
DNA change (hg38) g.136518187G>A
Published as NOTCH1(NM_017617.3):c.1205C>T (p.(Ser402Leu)), NOTCH1(NM_017617.5):c.1205C>T (p.S402L)
ISCN -
DB-ID NOTCH1_000326 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOTCH1 NM_017617.3 -?/. - c.1205C>T r.(?) p.(Ser402Leu)


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