NM_024809.5(TCTN2):c.1848C>T (p.Ser616=) AND Meckel syndrome, type 8
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000375557.5
Allele description [Variation Report for NM_024809.5(TCTN2):c.1848C>T (p.Ser616=)]
NM_024809.5(TCTN2):c.1848C>T (p.Ser616=)
Condition(s)
-
eggc.vipv0s (0)
BioProject
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Mar 5, 2024