NM_000251.3(MSH2):c.2150_2153del (p.Ser717fs) AND Lynch syndrome
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Dec 14, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000234418.2
Allele description [Variation Report for NM_000251.3(MSH2):c.2150_2153del (p.Ser717fs)]
NM_000251.3(MSH2):c.2150_2153del (p.Ser717fs)
Condition(s)
- Name:
- Lynch syndrome
- Identifiers:
- MONDO: MONDO:0005835; MedGen: C4552100
-
PREDICTED: Mus musculus ubiquitin specific peptidase 15 (Usp15), transcript vari...
PREDICTED: Mus musculus ubiquitin specific peptidase 15 (Usp15), transcript variant X5, mRNAgi|1907073494|ref|XM_006513227.5|Nucleotide
-
ubiquitin carboxyl-terminal hydrolase 15 isoform X5 [Mus musculus]
ubiquitin carboxyl-terminal hydrolase 15 isoform X5 [Mus musculus]gi|568966688|ref|XP_006513290.1|Protein
-
SH2 domain-containing adapter protein F isoform X1 [Cricetulus griseus]
SH2 domain-containing adapter protein F isoform X1 [Cricetulus griseus]gi|1868060524|ref|XP_003504830.3|Protein
-
PREDICTED: Cricetulus griseus Src homology 2 domain containing F (Shf), transcri...
PREDICTED: Cricetulus griseus Src homology 2 domain containing F (Shf), transcript variant X2, mRNAgi|1868353472|ref|XM_035446574.1|Nucleotide
-
SRX16367635 (1)
SRA
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Last Updated: Sep 29, 2024