NM_004573.3(PLCB2):c.3168G>T (p.Gln1056His) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 8, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004511762.1
Allele description [Variation Report for NM_004573.3(PLCB2):c.3168G>T (p.Gln1056His)]
NM_004573.3(PLCB2):c.3168G>T (p.Gln1056His)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
-
regulator of G protein signaling 14 [Homo sapiens]
regulator of G protein signaling 14 [Homo sapiens]gi|2247810489|gb|KAI4024097.1||gnl| AAKGM|cds.CHM13_T0182784Protein
-
06 com AND (3/8) (0)
BioProject
-
Component(Core) Links for Nucleotide (Select 1843978382) (4)
Nucleotide
-
RefSeq RNA Links for Gene (Select 8634) (2)
Nucleotide
-
Nucleotide Links for Protein (Select 260436928) (3)
Nucleotide
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See more...Assertion and evidence details
Last Updated: May 7, 2024