NM_001440.4(EXTL3):c.510C>A (p.Pro170=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002075315.6
Allele description [Variation Report for NM_001440.4(EXTL3):c.510C>A (p.Pro170=)]
NM_001440.4(EXTL3):c.510C>A (p.Pro170=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens cDNA: FLJ22696 fis, clone HSI11696
Homo sapiens cDNA: FLJ22696 fis, clone HSI11696gi|10439188|dbj|AK026349.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024