NM_005422.4(TECTA):c.3619G>A (p.Val1207Met) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003165547.2
Allele description [Variation Report for NM_005422.4(TECTA):c.3619G>A (p.Val1207Met)]
NM_005422.4(TECTA):c.3619G>A (p.Val1207Met)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Pathogen: clinical or host-associated sample from Streptococcus suis
Pathogen: clinical or host-associated sample from Streptococcus suisbiosample
-
BioSample links for Nucleotide (Select 1993406460) (1)
BioSample
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Last Updated: May 1, 2024