NM_007373.4(SHOC2):c.663C>T (p.Ser221=) AND RASopathy
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 21, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003655666.1
Allele description [Variation Report for NM_007373.4(SHOC2):c.663C>T (p.Ser221=)]
NM_007373.4(SHOC2):c.663C>T (p.Ser221=)
Condition(s)
- Name:
- RASopathy
- Synonyms:
- rasopathies; Noonan spectrum disorder
- Identifiers:
- MONDO: MONDO:0021060; MedGen: C5555857
-
HSD17B4 [Mustela nigripes]
HSD17B4 [Mustela nigripes]Gene ID:132027375Gene
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Feb 28, 2024