NM_002335.4(LRP5):c.31C>T (p.Pro11Ser) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004042501.1
Allele description [Variation Report for NM_002335.4(LRP5):c.31C>T (p.Pro11Ser)]
NM_002335.4(LRP5):c.31C>T (p.Pro11Ser)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Concise Conserved Domain Links for Protein (Select 585136219) (1)
Conserved Domains
-
txid1802692[Organism:noexp] (895)
Identical Protein Groups
-
Boechera repanda voucher NMC:P.J. Alexander 845b MPS35 gene, partial sequence
Boechera repanda voucher NMC:P.J. Alexander 845b MPS35 gene, partial sequencegi|401018135|gb|JX146496.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024