NM_007373.4(SHOC2):c.568A>G (p.Arg190Gly) AND RASopathy
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002571854.3
Allele description [Variation Report for NM_007373.4(SHOC2):c.568A>G (p.Arg190Gly)]
NM_007373.4(SHOC2):c.568A>G (p.Arg190Gly)
Condition(s)
- Name:
- RASopathy
- Synonyms:
- rasopathies; Noonan spectrum disorder
- Identifiers:
- MONDO: MONDO:0021060; MedGen: C5555857
-
SRX24348373 (1)
SRA
-
GALNTL6 [Pelodiscus sinensis]
GALNTL6 [Pelodiscus sinensis]Gene ID:102455074Gene
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Last Updated: Sep 29, 2024