NM_004560.4(ROR2):c.1279A>G (p.Met427Val) AND Autosomal recessive Robinow syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001166325.4
Allele description [Variation Report for NM_004560.4(ROR2):c.1279A>G (p.Met427Val)]
NM_004560.4(ROR2):c.1279A>G (p.Met427Val)
Condition(s)
-
Full text in PMC (nucleotide) for Gene (Select 3238873) (3)
PMC
-
SRA Links for BioSample (Select 8886167) (1)
SRA
-
txid690078[Organism:noexp] (1)
Identical Protein Groups
-
MAG TPA_asm: Bacteriophage sp. isolate ctxXv26, partial genome
MAG TPA_asm: Bacteriophage sp. isolate ctxXv26, partial genomegi|2054406863|tpg|BK054573.1|Nucleotide
-
txid662736[Organism] (672)
Nucleotide
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See more...Assertion and evidence details
Last Updated: Mar 5, 2024