ClinVar

NM_006186.4(NR4A2):c.717C>T (p.His239=)

Gene:

NR4A2:nuclear receptor subfamily 4 group A member 2 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

2q24.1

Genomic location:

• Chr2: 156329470 (on Assembly GRCh38)
• Chr2: 157185982 (on Assembly GRCh37)

Preferred name:

NM_006186.4(NR4A2):c.717C>T (p.His239=)

HGVS:

• NC_000002.12:g.156329470G>A
• NG_011821.1:g.8306C>T
• NG_011821.2:g.8251C>T
• NM_006186.4:c.717C>TMANE SELECT
• NM_173173.3:c.528C>T
• NP_006177.1:p.His239=
• NP_775265.1:p.His176=
• NC_000002.11:g.157185982G>A

This HGVS expression did not pass validation

Molecular consequence:

• NM_006186.4:c.717C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_173173.3:c.528C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

1