NM_000651.6(CR1):c.6325G>A (p.Gly2109Ser) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 3, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001813148.13
Allele description [Variation Report for NM_000651.6(CR1):c.6325G>A (p.Gly2109Ser)]
NM_000651.6(CR1):c.6325G>A (p.Gly2109Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
Homo sapiens proline rich 5 (PRR5), transcript variant 5, mRNA
Homo sapiens proline rich 5 (PRR5), transcript variant 5, mRNAgi|1890342707|ref|NM_001017529.3|Nucleotide
-
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See more...Assertion and evidence details
Last Updated: Sep 16, 2024