NM_173563.3(FAM217A):c.652T>C (p.Tyr218His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 6, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004381228.1
Allele description [Variation Report for NM_173563.3(FAM217A):c.652T>C (p.Tyr218His)]
NM_173563.3(FAM217A):c.652T>C (p.Tyr218His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens cut like homeobox 1 (CUX1), transcript variant 4, mRNA
Homo sapiens cut like homeobox 1 (CUX1), transcript variant 4, mRNAgi|1675178466|ref|NM_001202543.2|Nucleotide
-
PREDICTED: Homo sapiens chromosome 1 open reading frame 167 (C1orf167), transcri...
PREDICTED: Homo sapiens chromosome 1 open reading frame 167 (C1orf167), transcript variant X1, mRNAgi|2217266673|ref|XM_024446506.2|Nucleotide
-
MTND4LP28 MT-ND4L pseudogene 28 [Homo sapiens]
MTND4LP28 MT-ND4L pseudogene 28 [Homo sapiens]Gene ID:107133489Gene
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Last Updated: May 7, 2024