NM_001291303.3(FAT4):c.12043T>C (p.Tyr4015His) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 27, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002692493.2
Allele description [Variation Report for NM_001291303.3(FAT4):c.12043T>C (p.Tyr4015His)]
NM_001291303.3(FAT4):c.12043T>C (p.Tyr4015His)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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JGI_XZT40560.fwd NIH_XGC_tropTad5 Xenopus tropicalis cDNA clone IMAGE:7616486 5'...
JGI_XZT40560.fwd NIH_XGC_tropTad5 Xenopus tropicalis cDNA clone IMAGE:7616486 5', mRNA sequencegi|74095303|gnl|dbEST|31260677|gb|C 69.2|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024