NM_182758.4(WDR72):c.983A>G (p.Tyr328Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002817918.2
Allele description [Variation Report for NM_182758.4(WDR72):c.983A>G (p.Tyr328Cys)]
NM_182758.4(WDR72):c.983A>G (p.Tyr328Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
nerve pain (1002)
NLM Catalog
-
male antennae 3
male antennae 3biosample
-
AGENCOURT_14903601 NICHD_XGC_Emb8 Xenopus tropicalis cDNA clone IMAGE:6984706 5'...
AGENCOURT_14903601 NICHD_XGC_Emb8 Xenopus tropicalis cDNA clone IMAGE:6984706 5', mRNA sequencegi|33249842|gnl|dbEST|19310327|gb|C 34.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024