NM_001007561.3(IRGQ):c.94G>A (p.Val32Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 15, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004403298.1
Allele description [Variation Report for NM_001007561.3(IRGQ):c.94G>A (p.Val32Met)]
NM_001007561.3(IRGQ):c.94G>A (p.Val32Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
KAT8 regulatory NSL complex subunit 1-like protein isoform X1 [Homo sapiens]
KAT8 regulatory NSL complex subunit 1-like protein isoform X1 [Homo sapiens]gi|530369884|ref|XP_005246385.1|Protein
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See more...Assertion and evidence details
Last Updated: May 7, 2024