NM_000551.4(VHL):c.114C>T (p.Ser38=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 18, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000204195.15
Allele description [Variation Report for NM_000551.4(VHL):c.114C>T (p.Ser38=)]
NM_000551.4(VHL):c.114C>T (p.Ser38=)
Condition(s)
-
Homo sapiens colony stimulating factor 2 receptor subunit alpha (CSF2RA), transc...
Homo sapiens colony stimulating factor 2 receptor subunit alpha (CSF2RA), transcript variant 4, mRNAgi|1824163970|ref|NM_172247.3|Nucleotide
-
Homo sapiens FTSH gene for putative ATPases, exons 1 and 2 and join CDS
Homo sapiens FTSH gene for putative ATPases, exons 1 and 2 and join CDSgi|9506352|emb|AJ295618.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024