NM_152468.5(TMC8):c.2062G>C (p.Ala688Pro) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Sep 17, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002708261.2
Allele description [Variation Report for NM_152468.5(TMC8):c.2062G>C (p.Ala688Pro)]
NM_152468.5(TMC8):c.2062G>C (p.Ala688Pro)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Related DataSets for GEO Profiles (Select 59053138) (1)
GEO DataSets
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Synchronous and metachronous liver metastases from colorectal cancerAccession: GDS3501GEO DataSets
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txid60552[orgn] AND "strain FL-7-3-30-S2-D0"[All Fields] (184)
Nucleotide
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Last Updated: May 1, 2024