NM_001393578.1(MRGPRX1):c.895T>C (p.Ser299Pro) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004314846.1
Allele description [Variation Report for NM_001393578.1(MRGPRX1):c.895T>C (p.Ser299Pro)]
NM_001393578.1(MRGPRX1):c.895T>C (p.Ser299Pro)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
Homo sapiens fibronectin leucine rich transmembrane protein 2 (FLRT2), mRNA
Homo sapiens fibronectin leucine rich transmembrane protein 2 (FLRT2), mRNAgi|62241047|ref|NM_013231.4|Nucleotide
-
Homo sapiens fibronectin leucine rich transmembrane protein 2, mRNA (cDNA clone ...
Homo sapiens fibronectin leucine rich transmembrane protein 2, mRNA (cDNA clone MGC:161527 IMAGE:8991965), complete cdsgi|116497154|gb|BC126249.1|Nucleotide
-
Homo sapiens fibronectin leucine rich transmembrane protein 2 (FLRT2), transcrip...
Homo sapiens fibronectin leucine rich transmembrane protein 2 (FLRT2), transcript variant 3, mRNAgi|1677703454|ref|NM_013231.6|Nucleotide
-
LOC124906605 [Homo sapiens]
LOC124906605 [Homo sapiens]Gene ID:124906605Gene
-
LOC127456838 [Homo sapiens]
LOC127456838 [Homo sapiens]Gene ID:127456838Gene
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See more...Assertion and evidence details
Last Updated: Oct 8, 2024