NM_198253.3(TERT):c.2177C>T (p.Thr726Met) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 24, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001818203.11
Allele description [Variation Report for NM_198253.3(TERT):c.2177C>T (p.Thr726Met)]
NM_198253.3(TERT):c.2177C>T (p.Thr726Met)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
wn89a04.x1 NCI_CGAP_Ut1 Homo sapiens cDNA clone IMAGE:2452974 3', mRNA sequence
wn89a04.x1 NCI_CGAP_Ut1 Homo sapiens cDNA clone IMAGE:2452974 3', mRNA sequencegi|5658137|gnl|dbEST|3044147|gb|AI9 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024