NM_001367493.1(ARHGEF4):c.3915C>G (p.Ser1305Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004352694.1
Allele description [Variation Report for NM_001367493.1(ARHGEF4):c.3915C>G (p.Ser1305Arg)]
NM_001367493.1(ARHGEF4):c.3915C>G (p.Ser1305Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
LOC112469007 [Homo sapiens]
LOC112469007 [Homo sapiens]Gene ID:112469007Gene
-
LOC127884099 [Homo sapiens]
LOC127884099 [Homo sapiens]Gene ID:127884099Gene
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See more...Assertion and evidence details
Last Updated: Oct 13, 2024