NM_033056.4(PCDH15):c.5389C>T (p.Pro1797Ser) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 16, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002560192.1
Allele description [Variation Report for NM_033056.4(PCDH15):c.5389C>T (p.Pro1797Ser)]
NM_033056.4(PCDH15):c.5389C>T (p.Pro1797Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
-
breast cancer type 1 susceptibility protein isoform 103 [Homo sapiens]
breast cancer type 1 susceptibility protein isoform 103 [Homo sapiens]gi|2255444308|ref|NP_001395341.1|Protein
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Last Updated: Feb 7, 2023