ClinVar

NM_003560.4(PLA2G6):c.987C>A (p.Arg329=)

Gene:

PLA2G6:phospholipase A2 group VI [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

22q13.1

Genomic location:

• Chr22: 38132921 (on Assembly GRCh38)
• Chr22: 38528928 (on Assembly GRCh37)

Preferred name:

NM_003560.4(PLA2G6):c.987C>A (p.Arg329=)

HGVS:

• NC_000022.11:g.38132921G>T
• NG_007094.3:g.86858C>A
• NM_001004426.3:c.987C>A
• NM_001199562.3:c.987C>A
• NM_001349864.2:c.987C>A
• NM_001349865.2:c.987C>A
• NM_001349866.2:c.987C>A
• NM_001349867.2:c.453C>A
• NM_001349868.2:c.309C>A
• NM_001349869.2:c.453C>A
• NM_003560.4:c.987C>AMANE SELECT
• NP_001004426.1:p.Arg329=
• NP_001186491.1:p.Arg329=
• NP_001336793.1:p.Arg329=
• NP_001336794.1:p.Arg329=
• NP_001336795.1:p.Arg329=
• NP_001336796.1:p.Arg151=
• NP_001336797.1:p.Arg103=
• NP_001336798.1:p.Arg151=
• NP_003551.2:p.Arg329=
• LRG_1015t1:c.987C>A
• LRG_1015:g.86858C>A
• LRG_1015p1:p.Arg329=
• NC_000022.10:g.38528928G>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_001004426.3:c.987C>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001199562.3:c.987C>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349864.2:c.987C>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349865.2:c.987C>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349866.2:c.987C>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349867.2:c.453C>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349868.2:c.309C>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349869.2:c.453C>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_003560.4:c.987C>A - synonymous variant - [Sequence Ontology: SO:0001819]