NM_173651.4(FSIP2):c.8183C>G (p.Thr2728Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004618728.1
Allele description [Variation Report for NM_173651.4(FSIP2):c.8183C>G (p.Thr2728Arg)]
NM_173651.4(FSIP2):c.8183C>G (p.Thr2728Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
601452348F1 NIH_MGC_66 Homo sapiens cDNA clone IMAGE:3856355 5', mRNA sequence
601452348F1 NIH_MGC_66 Homo sapiens cDNA clone IMAGE:3856355 5', mRNA sequencegi|9894372|gnl|dbEST|5842234|gb|BE6 .1|
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See more...Assertion and evidence details
Last Updated: Aug 11, 2024