ClinVar

NM_002739.5(PRKCG):c.498G>T (p.Arg166=)

Gene:

PRKCG:protein kinase C gamma [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.42

Genomic location:

• Chr19: 53889986 (on Assembly GRCh38)
• Chr19: 54393240 (on Assembly GRCh37)

Preferred name:

NM_002739.5(PRKCG):c.498G>T (p.Arg166=)

HGVS:

• NC_000019.10:g.53889986G>T
• NG_009114.1:g.12774G>T
• NM_001316329.2:c.498G>T
• NM_002739.4:c.498G>T
• NM_002739.5:c.498G>TMANE SELECT
• NP_001303258.1:p.Arg166=
• NP_002730.1:p.Arg166=
• LRG_669t1:c.498G>T
• LRG_669:g.12774G>T
• NC_000019.9:g.54393240G>T
• NM_002739.3:c.498G>T

This HGVS expression did not pass validation

Links:

dbSNP: rs148370843

NCBI 1000 Genomes Browser:

rs148370843

Molecular consequence:

• NM_001316329.2:c.498G>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_002739.5:c.498G>T - synonymous variant - [Sequence Ontology: SO:0001819]