NM_016568.3(RXFP3):c.277G>A (p.Ala93Thr) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 19, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004447132.1
Allele description [Variation Report for NM_016568.3(RXFP3):c.277G>A (p.Ala93Thr)]
NM_016568.3(RXFP3):c.277G>A (p.Ala93Thr)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
DUF927 domain-containing protein [Escherichia coli]
DUF927 domain-containing protein [Escherichia coli]gi|446684444|ref|WP_000761790.1|Protein
-
PREDICTED: Homo sapiens annexin A11 (ANXA11), transcript variant X4, mRNA
PREDICTED: Homo sapiens annexin A11 (ANXA11), transcript variant X4, mRNAgi|2217276940|ref|XM_006717813.3|Nucleotide
-
Homo sapiens cDNA FLJ12254 fis, clone MAMMA1001465
Homo sapiens cDNA FLJ12254 fis, clone MAMMA1001465gi|10433685|dbj|AK022316.1|Nucleotide
-
Homo sapiens annexin A11 mRNA, complete cds
Homo sapiens annexin A11 mRNA, complete cdsgi|54696729|gnl|clontech|GH01199X1. BT019934.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024