ClinVar

NM_003560.4(PLA2G6):c.441G>A (p.Ala147=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

22q13.1

Genomic location:

• Chr22: 38143273 (on Assembly GRCh38)
• Chr22: 38539280 (on Assembly GRCh37)

Preferred name:

NM_003560.4(PLA2G6):c.441G>A (p.Ala147=)

HGVS:

• NC_000022.11:g.38143273C>T
• NG_007094.3:g.76506G>A
• NM_001004426.3:c.441G>A
• NM_001199562.3:c.441G>A
• NM_001349864.2:c.441G>A
• NM_001349865.2:c.441G>A
• NM_001349866.2:c.441G>A
• NM_001349867.2:c.-94G>A
• NM_001349868.2:c.-50G>A
• NM_001349869.2:c.-94G>A
• NM_003560.4:c.441G>AMANE SELECT
• NP_001004426.1:p.Ala147=
• NP_001186491.1:p.Ala147=
• NP_001336793.1:p.Ala147=
• NP_001336794.1:p.Ala147=
• NP_001336795.1:p.Ala147=
• NP_003551.2:p.Ala147=
• LRG_1015t1:c.441G>A
• LRG_1015:g.76506G>A
• LRG_1015p1:p.Ala147=
• NC_000022.10:g.38539280C>T
• NG_007094.2:g.67418G>A
• NM_003560.2:c.441G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs371920697

NCBI 1000 Genomes Browser:

rs371920697

Molecular consequence:

• NM_001349867.2:c.-94G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001349868.2:c.-50G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001349869.2:c.-94G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001004426.3:c.441G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001199562.3:c.441G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349864.2:c.441G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349865.2:c.441G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001349866.2:c.441G>A - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_003560.4:c.441G>A - synonymous variant - [Sequence Ontology: SO:0001819]