NM_014319.5(LEMD3):c.2006T>C (p.Met669Thr) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 18, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003106745.4
Allele description [Variation Report for NM_014319.5(LEMD3):c.2006T>C (p.Met669Thr)]
NM_014319.5(LEMD3):c.2006T>C (p.Met669Thr)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens cDNA clone IMAGE:4388353
Homo sapiens cDNA clone IMAGE:4388353gi|21707482|gb|BC033834.1|Nucleotide
-
AGENCOURT_6542488 NIH_MGC_119 Homo sapiens cDNA clone IMAGE:5742683 5', mRNA seq...
AGENCOURT_6542488 NIH_MGC_119 Homo sapiens cDNA clone IMAGE:5742683 5', mRNA sequencegi|18791048|gnl|dbEST|11125227|gb|B 40.1|Nucleotide
-
Homo sapiens solute carrier family 25, member 37, mRNA (cDNA clone MGC:164430 IM...
Homo sapiens solute carrier family 25, member 37, mRNA (cDNA clone MGC:164430 IMAGE:40146821), complete cdsgi|124376585|gb|BC132799.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Sep 29, 2024