NM_030973.4(MED25):c.597C>T (p.Ala199=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 9, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000428612.1
Allele description [Variation Report for NM_030973.4(MED25):c.597C>T (p.Ala199=)]
NM_030973.4(MED25):c.597C>T (p.Ala199=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens integrin, alpha M (complement component 3 receptor 3 subunit), mRNA...
Homo sapiens integrin, alpha M (complement component 3 receptor 3 subunit), mRNA (cDNA clone MGC:117044 IMAGE:40008969), complete cdsgi|109730155|gb|BC099660.3|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024