NM_173628.4(DNAH17):c.4296G>A (p.Pro1432=) AND DNAH17-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 6, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003959583.2
Allele description [Variation Report for NM_173628.4(DNAH17):c.4296G>A (p.Pro1432=)]
NM_173628.4(DNAH17):c.4296G>A (p.Pro1432=)
Condition(s)
- Name:
- DNAH17-related disorder
- Synonyms:
- DNAH17-related condition
- Identifiers:
-
Homo sapiens regulator of G protein signaling 18 (RGS18), mRNA
Homo sapiens regulator of G protein signaling 18 (RGS18), mRNAgi|1519243348|ref|NM_130782.3|Nucleotide
-
LOC124907423 [Homo sapiens]
LOC124907423 [Homo sapiens]Gene ID:124907423Gene
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Last Updated: Oct 8, 2024