NM_001059.3(TACR3):c.892G>A (p.Val298Ile) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 20, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000500874.6
Allele description [Variation Report for NM_001059.3(TACR3):c.892G>A (p.Val298Ile)]
NM_001059.3(TACR3):c.892G>A (p.Val298Ile)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Abnormal digestive system morphology
Abnormal digestive system morphologyMedGen
-
Peroxisome biogenesis disorder 4B
Peroxisome biogenesis disorder 4BMedGen
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See more...Assertion and evidence details
Last Updated: Oct 14, 2023