NM_138694.4(PKHD1):c.10883C>T (p.Thr3628Ile) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003992452.6
Allele description [Variation Report for NM_138694.4(PKHD1):c.10883C>T (p.Thr3628Ile)]
NM_138694.4(PKHD1):c.10883C>T (p.Thr3628Ile)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens astrotactin 2 (ASTN2), transcript variant 2, mRNA
Homo sapiens astrotactin 2 (ASTN2), transcript variant 2, mRNAgi|296080726|ref|NM_198186.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024