NM_000179.3(MSH6):c.2413A>T (p.Ile805Phe) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Apr 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000571872.6
Allele description [Variation Report for NM_000179.3(MSH6):c.2413A>T (p.Ile805Phe)]
NM_000179.3(MSH6):c.2413A>T (p.Ile805Phe)
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
-
Polystichum polyblepharum var. scabiosum chloroplast DNA, psbA-trnH intergenic s...
Polystichum polyblepharum var. scabiosum chloroplast DNA, psbA-trnH intergenic spacer, partial sequence, specimen_voucher: TNS:764356gi|313474824|dbj|AB575831.1|Nucleotide
-
Homo sapiens butyrophilin subfamily 3 member A3 (BTN3A3), transcript variant 2, ...
Homo sapiens butyrophilin subfamily 3 member A3 (BTN3A3), transcript variant 2, mRNAgi|1676319837|ref|NM_197974.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024