NM_000156.6(GAMT):c.187C>T (p.Arg63Trp) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 16, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004035647.1
Allele description [Variation Report for NM_000156.6(GAMT):c.187C>T (p.Arg63Trp)]
NM_000156.6(GAMT):c.187C>T (p.Arg63Trp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
CBTC10691.rev NICHD_XGC_tropBone1 Xenopus tropicalis cDNA clone IMAGE:8941260 3'...
CBTC10691.rev NICHD_XGC_tropBone1 Xenopus tropicalis cDNA clone IMAGE:8941260 3', mRNA sequencegi|126259436|gnl|dbEST|45033100|gb| 548.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024