NM_001384479.1(AGT):c.914C>G (p.Ser305Cys) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002953935.3
Allele description [Variation Report for NM_001384479.1(AGT):c.914C>G (p.Ser305Cys)]
NM_001384479.1(AGT):c.914C>G (p.Ser305Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
LOC127407269 [Homo sapiens]
LOC127407269 [Homo sapiens]Gene ID:127407269Gene
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024