NM_003242.6(TGFBR2):c.1587C>T (p.Leu529=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000935462.21
Allele description [Variation Report for NM_003242.6(TGFBR2):c.1587C>T (p.Leu529=)]
NM_003242.6(TGFBR2):c.1587C>T (p.Leu529=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
-
PubChem Compound Links for Gene (Select 11064) (34)
PubChem Compound
-
centriolin isoform X18 [Homo sapiens]
centriolin isoform X18 [Homo sapiens]gi|2217375266|ref|XP_047278640.1|Protein
-
PREDICTED: Homo sapiens centriolin (CNTRL), transcript variant X25, mRNA
PREDICTED: Homo sapiens centriolin (CNTRL), transcript variant X25, mRNAgi|2462622356|ref|XM_054361841.1|Nucleotide
-
PREDICTED: Homo sapiens centriolin (CNTRL), transcript variant X29, mRNA
PREDICTED: Homo sapiens centriolin (CNTRL), transcript variant X29, mRNAgi|2217375277|ref|XM_017014224.3|Nucleotide
-
PREDICTED: Homo sapiens centriolin (CNTRL), transcript variant X14, mRNA
PREDICTED: Homo sapiens centriolin (CNTRL), transcript variant X14, mRNAgi|2462622334|ref|XM_054361830.1|Nucleotide
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Last Updated: Oct 8, 2024