NM_016279.4(CDH9):c.1700C>T (p.Pro567Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 12, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004351755.1
Allele description [Variation Report for NM_016279.4(CDH9):c.1700C>T (p.Pro567Leu)]
NM_016279.4(CDH9):c.1700C>T (p.Pro567Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
za75h08.s1 Soares_fetal_lung_NbHL19W Homo sapiens cDNA clone IMAGE:298431 3', mR...
za75h08.s1 Soares_fetal_lung_NbHL19W Homo sapiens cDNA clone IMAGE:298431 3', mRNA sequencegi|1231420|gnl|dbEST|480272|gb|N741Nucleotide
-
Homo sapiens casein alpha s1 (CSN1S1), transcript variant 2, mRNA
Homo sapiens casein alpha s1 (CSN1S1), transcript variant 2, mRNAgi|1675116695|ref|NM_001025104.2|Nucleotide
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Last Updated: Oct 13, 2024