NM_014874.4(MFN2):c.975C>T (p.Gly325=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Sep 9, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000173866.5
Allele description [Variation Report for NM_014874.4(MFN2):c.975C>T (p.Gly325=)]
NM_014874.4(MFN2):c.975C>T (p.Gly325=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Drosophila melanogaster uncharacterized protein, transcript variant B (CG4168), ...
Drosophila melanogaster uncharacterized protein, transcript variant B (CG4168), mRNAgi|665408143|ref|NM_135896.6|Nucleotide
-
AGENCOURT_8042786 NIH_MGC_112 Homo sapiens cDNA clone IMAGE:6090211 5', mRNA seq...
AGENCOURT_8042786 NIH_MGC_112 Homo sapiens cDNA clone IMAGE:6090211 5', mRNA sequencegi|22280459|gnl|dbEST|13180494|gb|B 45.1|Nucleotide
-
602034422F1 NCI_CGAP_Brn64 Homo sapiens cDNA clone IMAGE:4182652 5', mRNA sequen...
602034422F1 NCI_CGAP_Brn64 Homo sapiens cDNA clone IMAGE:4182652 5', mRNA sequencegi|11283128|gnl|dbEST|6783943|gb|BF 2.1|Nucleotide
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Last Updated: Feb 20, 2024