NM_001796.5(CDH8):c.1996C>T (p.Arg666Cys) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000882254.4
Allele description [Variation Report for NM_001796.5(CDH8):c.1996C>T (p.Arg666Cys)]
NM_001796.5(CDH8):c.1996C>T (p.Arg666Cys)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Chromosome neighbors for GEO Profiles (Select 77981197) (20)
GEO Profiles
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Chromosome neighbors for GEO Profiles (Select 6925016) (1)
GEO Profiles
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Homo sapiens
Homo sapiensRefSeq annotation of the human reference genome assemblyBioProject
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Homo sapiens nei like DNA glycosylase 2 (NEIL2), transcript variant 8, mRNA
Homo sapiens nei like DNA glycosylase 2 (NEIL2), transcript variant 8, mRNAgi|1676320103|ref|NM_001349442.2|Nucleotide
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Homo sapiens chromosome 8 genomic patch of type FIX, GRCh38.p14 PATCHES HG76_PAT...
Homo sapiens chromosome 8 genomic patch of type FIX, GRCh38.p14 PATCHES HG76_PATCHgi|1208651610|gnl|ASM:GCF_000005045 G76_PATCH|ref|NW_018654717.1|Nucleotide
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Last Updated: Dec 24, 2023