ClinVar

NM_152296.5(ATP1A3):c.1683C>T (p.Phe561=)

Gene:

ATP1A3:ATPase Na+/K+ transporting subunit alpha 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.2

Genomic location:

• Chr19: 41978274 (on Assembly GRCh38)
• Chr19: 42482426 (on Assembly GRCh37)

Preferred name:

NM_152296.5(ATP1A3):c.1683C>T (p.Phe561=)

HGVS:

• NC_000019.10:g.41978274G>A
• NG_008015.1:g.20957C>T
• NM_001256213.2:c.1716C>T
• NM_001256214.2:c.1722C>T
• NM_152296.5:c.1683C>TMANE SELECT
• NP_001243142.1:p.Phe572=
• NP_001243143.1:p.Phe574=
• NP_689509.1:p.Phe561=
• LRG_1186t1:c.1683C>T
• LRG_1186:g.20957C>T
• LRG_1186p1:p.Phe561=
• NC_000019.9:g.42482426G>A

This HGVS expression did not pass validation

Links:

dbSNP: rs781866390

NCBI 1000 Genomes Browser:

rs781866390

Molecular consequence:

• NM_001256213.2:c.1716C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001256214.2:c.1722C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_152296.5:c.1683C>T - synonymous variant - [Sequence Ontology: SO:0001819]