NM_000124.4(ERCC6):c.718A>G (p.Ile240Val) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003261963.2
Allele description [Variation Report for NM_000124.4(ERCC6):c.718A>G (p.Ile240Val)]
NM_000124.4(ERCC6):c.718A>G (p.Ile240Val)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
CCNYL1 cyclin Y like 1 [Homo sapiens]
CCNYL1 cyclin Y like 1 [Homo sapiens]Gene ID:151195Gene
-
Gene Links for GEO Profiles (Select 65669536) (1)
Gene
-
NOTCH antagonist SAHM1 effect on T-ALL cell lines
NOTCH antagonist SAHM1 effect on T-ALL cell linesAccession: GDS3717GEO DataSets
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Related DataSets for GEO Profiles (Select 65678181) (1)
GEO DataSets
-
LOC127825625 [Homo sapiens]
LOC127825625 [Homo sapiens]Gene ID:127825625Gene
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Last Updated: May 1, 2024