NM_032436.4(CHAMP1):c.979C>A (p.Pro327Thr) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 16, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002849275.2
Allele description [Variation Report for NM_032436.4(CHAMP1):c.979C>A (p.Pro327Thr)]
NM_032436.4(CHAMP1):c.979C>A (p.Pro327Thr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
CBST10200.rev NICHD_XGC_tropThy1 Xenopus tropicalis cDNA clone IMAGE:8930720 3',...
CBST10200.rev NICHD_XGC_tropThy1 Xenopus tropicalis cDNA clone IMAGE:8930720 3', mRNA sequencegi|126545086|gnl|dbEST|45058957|gb| 598.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 1, 2024