NM_012123.4(MTO1):c.446C>A (p.Thr149Asn) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 14, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004646808.1
Allele description [Variation Report for NM_012123.4(MTO1):c.446C>A (p.Thr149Asn)]
NM_012123.4(MTO1):c.446C>A (p.Thr149Asn)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
nssv2845177 (0)
GEO DataSets
-
NADH dehydrogenase subunit F, partial (plastid) [Linaria spartea]
NADH dehydrogenase subunit F, partial (plastid) [Linaria spartea]gi|700212455|gb|AIU47886.1|Protein
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Aug 11, 2024