ClinVar

NM_003501.3(ACOX3):c.1306C>T (p.Arg436Trp)

Gene:

ACOX3:acyl-CoA oxidase 3, pristanoyl [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

4p16.1

Genomic location:

• Chr4: 8389729 (on Assembly GRCh38)
• Chr4: 8391456 (on Assembly GRCh37)

Preferred name:

NM_003501.3(ACOX3):c.1306C>T (p.Arg436Trp)

HGVS:

• NC_000004.12:g.8389729G>A
• NM_001101667.2:c.1306C>T
• NM_001375783.1:c.1306C>T
• NM_001375784.1:c.1234C>T
• NM_001375785.1:c.1306C>T
• NM_001375786.1:c.1306C>T
• NM_001375787.1:c.1306C>T
• NM_001375788.1:c.1306C>T
• NM_001375789.1:c.1021C>T
• NM_001375790.1:c.1306C>T
• NM_003501.3:c.1306C>TMANE SELECT
• NP_001095137.1:p.Arg436Trp
• NP_001362712.1:p.Arg436Trp
• NP_001362713.1:p.Arg412Trp
• NP_001362714.1:p.Arg436Trp
• NP_001362715.1:p.Arg436Trp
• NP_001362716.1:p.Arg436Trp
• NP_001362717.1:p.Arg436Trp
• NP_001362718.1:p.Arg341Trp
• NP_001362719.1:p.Arg436Trp
• NP_003492.2:p.Arg436Trp
• NC_000004.11:g.8391456G>A
• NM_003501.2:c.1306C>T

This HGVS expression did not pass validation

Protein change:

R341W

Molecular consequence:

• NM_001101667.2:c.1306C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001375783.1:c.1306C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001375784.1:c.1234C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001375785.1:c.1306C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001375786.1:c.1306C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001375787.1:c.1306C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001375788.1:c.1306C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001375789.1:c.1021C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001375790.1:c.1306C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_003501.3:c.1306C>T - missense variant - [Sequence Ontology: SO:0001583]