NM_000038.6(APC):c.3378C>G (p.Ser1126Arg) AND not specified
- Germline classification:
- Likely benign (4 submissions)
- Last evaluated:
- Jan 5, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000120024.18
Allele description [Variation Report for NM_000038.6(APC):c.3378C>G (p.Ser1126Arg)]
NM_000038.6(APC):c.3378C>G (p.Ser1126Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens WD repeat domain, phosphoinositide interacting 2 (WIPI2), transcrip...
Homo sapiens WD repeat domain, phosphoinositide interacting 2 (WIPI2), transcript variant 1, mRNAgi|75677333|ref|NM_015610.3|Nucleotide
-
Homo sapiens GTP-binding protein ROC1 (ROC1) mRNA, complete cds
Homo sapiens GTP-binding protein ROC1 (ROC1) mRNA, complete cdsgi|4234917|gb|AF084462.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024