NM_021625.5(TRPV4):c.1038C>T (p.Tyr346=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 11, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002393013.2
Allele description [Variation Report for NM_021625.5(TRPV4):c.1038C>T (p.Tyr346=)]
NM_021625.5(TRPV4):c.1038C>T (p.Tyr346=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
RC5-NN1065-180400-031-A02 NN1065 Homo sapiens cDNA, mRNA sequence
RC5-NN1065-180400-031-A02 NN1065 Homo sapiens cDNA, mRNA sequencegi|8069054|gnl|dbEST|4391581|gb|AW9 .1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024