NM_024675.4(PALB2):c.113C>T (p.Ala38Val) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- May 18, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000774648.8
Allele description [Variation Report for NM_024675.4(PALB2):c.113C>T (p.Ala38Val)]
NM_024675.4(PALB2):c.113C>T (p.Ala38Val)
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
-
ATP synthase F0 subunit 8 (mitochondrion) [Papilio memnon]
ATP synthase F0 subunit 8 (mitochondrion) [Papilio memnon]gi|1690540945|gb|QDE12975.1|Protein
-
unconventional myosin-XVI isoform X2 [Mus musculus]
unconventional myosin-XVI isoform X2 [Mus musculus]gi|568953285|ref|XP_006508842.1|Protein
-
C629_RS14245 [Corynebacterium glutamicum SCgG2]
C629_RS14245 [Corynebacterium glutamicum SCgG2]Gene ID:69623143Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024