NM_001048174.2(MUTYH):c.389C>T (p.Thr130Ile) AND Hereditary cancer-predisposing syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 21, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002334112.2
Allele description [Variation Report for NM_001048174.2(MUTYH):c.389C>T (p.Thr130Ile)]
NM_001048174.2(MUTYH):c.389C>T (p.Thr130Ile)
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
-
protein C3orf33 isoform 2 [Homo sapiens]
protein C3orf33 isoform 2 [Homo sapiens]gi|27734925|ref|NP_775928.1|Protein
-
xl11036E09R_1352112 Xenopus ORFeome version 1.0 library Xenopus laevis cDNA clon...
xl11036E09R_1352112 Xenopus ORFeome version 1.0 library Xenopus laevis cDNA clone xl11036E09 3', mRNA sequencegi|798033098|gnl|dbEST|79644672|gb| 970.1|Nucleotide
-
xl11050E05F_1373864 Xenopus ORFeome version 1.0 library Xenopus laevis cDNA clon...
xl11050E05F_1373864 Xenopus ORFeome version 1.0 library Xenopus laevis cDNA clone xl11050E05 5', mRNA sequencegi|798022559|gnl|dbEST|79646168|gb| 466.1|Nucleotide
-
GPC2 glypican 2 [Homo sapiens]
GPC2 glypican 2 [Homo sapiens]Gene ID:221914Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: May 1, 2024