NM_000251.3(MSH2):c.2635-11A>G AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Conflicting interpretations of pathogenicity (2 submissions)
- Last evaluated:
- Sep 18, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000583741.6
Allele description [Variation Report for NM_000251.3(MSH2):c.2635-11A>G]
NM_000251.3(MSH2):c.2635-11A>G
Condition(s)
- Name:
- Hereditary cancer-predisposing syndrome
- Synonyms:
- Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672
-
serine hydroxymethyltransferase 7-like [Cucurbita pepo subsp. pepo]
serine hydroxymethyltransferase 7-like [Cucurbita pepo subsp. pepo]gi|1333102004|ref|XP_023524836.1|Protein
-
PREDICTED: cytochrome P450 71B37-like [Cucumis sativus]
PREDICTED: cytochrome P450 71B37-like [Cucumis sativus]gi|778704874|ref|XP_004135495.2|Protein
-
PREDICTED: uncharacterized protein LOC103947859 isoform X2 [Pyrus x bretschneide...
PREDICTED: uncharacterized protein LOC103947859 isoform X2 [Pyrus x bretschneideri]gi|694332981|ref|XP_009357101.1|Protein
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024