NM_001103.4(ACTN2):c.569T>G (p.Ile190Ser) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 16, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003802281.1
Allele description [Variation Report for NM_001103.4(ACTN2):c.569T>G (p.Ile190Ser)]
NM_001103.4(ACTN2):c.569T>G (p.Ile190Ser)
Condition(s)
-
0020-1383[ISSN] (1)
NLM Catalog
-
Homo sapiens granulin, mRNA (cDNA clone MGC:8480 IMAGE:2821810), complete cds
Homo sapiens granulin, mRNA (cDNA clone MGC:8480 IMAGE:2821810), complete cdsgi|33875303|gb|BC000324.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: Mar 5, 2024