ClinVar

NM_015690.5(STK36):c.1527C>T (p.Leu509=)

Gene:

STK36:serine/threonine kinase 36 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q35

Genomic location:

• Chr2: 218688843 (on Assembly GRCh38)
• Chr2: 219553566 (on Assembly GRCh37)

Preferred name:

NM_015690.5(STK36):c.1527C>T (p.Leu509=)

HGVS:

• NC_000002.12:g.218688843C>T
• NG_029739.1:g.21818C>T
• NM_001243313.2:c.1527C>T
• NM_001369423.1:c.1527C>T
• NM_015690.5:c.1527C>TMANE SELECT
• NP_001230242.1:p.Leu509=
• NP_001356352.1:p.Leu509=
• NP_056505.2:p.Leu509=
• NC_000002.11:g.219553566C>T
• NM_015690.4:c.1527C>T

This HGVS expression did not pass validation

Molecular consequence:

• NM_001243313.2:c.1527C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001369423.1:c.1527C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_015690.5:c.1527C>T - synonymous variant - [Sequence Ontology: SO:0001819]