NM_000249.4(MLH1):c.96C>G (p.Ile32Met) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (3 submissions)
- Last evaluated:
- May 12, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000581627.7
Allele description [Variation Report for NM_000249.4(MLH1):c.96C>G (p.Ile32Met)]
NM_000249.4(MLH1):c.96C>G (p.Ile32Met)
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
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alpha-(1,3)-fucosyltransferase 7-like isoform X2 [Acipenser ruthenus]
alpha-(1,3)-fucosyltransferase 7-like isoform X2 [Acipenser ruthenus]gi|2565173586|ref|XP_058842669.1|Protein
-
CHPF2 [Chlorocebus sabaeus]
CHPF2 [Chlorocebus sabaeus]Gene ID:103227251Gene
-
PISD [Chlorocebus sabaeus]
PISD [Chlorocebus sabaeus]Gene ID:103223189Gene
-
Pancrustacea spalt gene, partial cds.
Pancrustacea spalt gene, partial cds.PopSet: 2569155852PopSet
-
PopSet Links for Nucleotide (Select 2569157974) (1)
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See more...Assertion and evidence details
Last Updated: May 7, 2024