ClinVar

NM_003560.4(PLA2G6):c.1530C>T (p.Asp510=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

22q13.1

Genomic location:

• Chr22: 38123156 (on Assembly GRCh38)
• Chr22: 38519163 (on Assembly GRCh37)

Preferred name:

NM_003560.4(PLA2G6):c.1530C>T (p.Asp510=)

HGVS:

• NC_000022.11:g.38123156G>A
• NG_007094.3:g.96623C>T
• NG_145728.1:g.655G>A
• NM_001004426.3:c.1368C>T
• NM_001199562.3:c.1368C>T
• NM_001349864.2:c.1530C>T
• NM_001349865.2:c.1368C>T
• NM_001349866.2:c.1368C>T
• NM_001349867.2:c.996C>T
• NM_001349868.2:c.852C>T
• NM_001349869.2:c.834C>T
• NM_003560.4:c.1530C>TMANE SELECT
• NP_001004426.1:p.Asp456=
• NP_001186491.1:p.Asp456=
• NP_001336793.1:p.Asp510=
• NP_001336794.1:p.Asp456=
• NP_001336795.1:p.Asp456=
• NP_001336796.1:p.Asp332=
• NP_001336797.1:p.Asp284=
• NP_001336798.1:p.Asp278=
• NP_003551.2:p.Asp510=
• LRG_1015t1:c.1530C>T
• LRG_1015:g.96623C>T
• LRG_1015p1:p.Asp510=
• NC_000022.10:g.38519163G>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_001004426.3:c.1368C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001199562.3:c.1368C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349864.2:c.1530C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349865.2:c.1368C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349866.2:c.1368C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349867.2:c.996C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349868.2:c.852C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349869.2:c.834C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_003560.4:c.1530C>T - synonymous variant - [Sequence Ontology: SO:0001819]