NM_000535.7(PMS2):c.78_107del (p.Cys27_Ser36del) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 2, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000581223.3
Allele description [Variation Report for NM_000535.7(PMS2):c.78_107del (p.Cys27_Ser36del)]
NM_000535.7(PMS2):c.78_107del (p.Cys27_Ser36del)
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
-
da78g10.y1 Harland stage 19-23 Xenopus laevis cDNA clone IMAGE:3201090 5' simila...
da78g10.y1 Harland stage 19-23 Xenopus laevis cDNA clone IMAGE:3201090 5' similar to gb:D90151 Mouse mRNA for CArG-binding factor-A, complete cds (MOUSE), mRNA sequencegi|7699586|gnl|dbEST|4228630|gb|AW7 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Dec 24, 2023