ClinVar

NM_024420.3(PLA2G4A):c.559-17C>T

Gene:

PLA2G4A:phospholipase A2 group IVA [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1q31.1

Genomic location:

• Chr1: 186932746 (on Assembly GRCh38)
• Chr1: 186901878 (on Assembly GRCh37)

Preferred name:

NM_024420.3(PLA2G4A):c.559-17C>T

HGVS:

• NC_000001.11:g.186932746C>T
• NG_012203.2:g.108847C>T
• NM_001311193.2:c.379-17C>T
• NM_024420.3:c.559-17C>TMANE SELECT
• LRG_596t1:c.559-17C>T
• LRG_596:g.108847C>T
• NC_000001.10:g.186901878C>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_001311193.2:c.379-17C>T - intron variant - [Sequence Ontology: SO:0001627]
• NM_024420.3:c.559-17C>T - intron variant - [Sequence Ontology: SO:0001627]