Variant #0000612022 (NC_000009.11:g.139413126_139413127del, NM_017617.3:c.1017_1018del (NOTCH1))

Chromosome 9
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.139413126_139413127del
DNA change (hg38) g.136518674_136518675del
Published as NOTCH1(NM_017617.5):c.1017_1018delTG (p.A340Qfs*12)
ISCN -
DB-ID NOTCH1_000372
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-26 12:43:49 +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.1017_1018del r.(?) p.(Ala340GlnfsTer12)


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