ClinVar

NM_000218.3(KCNQ1):c.1556G>A (p.Arg519His)

Gene:

KCNQ1:potassium voltage-gated channel subfamily Q member 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.5

Genomic location:

• Chr11: 2768885 (on Assembly GRCh38)
• Chr11: 2790115 (on Assembly GRCh37)

Preferred name:

NM_000218.3(KCNQ1):c.1556G>A (p.Arg519His)

HGVS:

• NC_000011.10:g.2768885G>A
• NG_008935.1:g.328895G>A
• NM_000218.3:c.1556G>AMANE SELECT
• NM_001406836.1:c.1460G>A
• NM_001406837.1:c.1286G>A
• NM_001406838.1:c.1016G>A
• NM_181798.2:c.1175G>A
• NP_000209.2:p.Arg519His
• NP_000209.2:p.Arg519His
• NP_001393765.1:p.Arg487His
• NP_001393766.1:p.Arg429His
• NP_001393767.1:p.Arg339His
• NP_861463.1:p.Arg392His
• NP_861463.1:p.Arg392His
• LRG_287t1:c.1556G>A
• LRG_287t2:c.1175G>A
• LRG_287:g.328895G>A
• LRG_287p1:p.Arg519His
• LRG_287p2:p.Arg392His
• NC_000011.9:g.2790115G>A
• NM_000218.2:c.1556G>A
• NM_181798.1:c.1175G>A
• NR_040711.2:n.1449G>A

This HGVS expression did not pass validation

Protein change:

R339H

Links:

dbSNP: rs199472788

NCBI 1000 Genomes Browser:

rs199472788

Molecular consequence:

• NM_000218.3:c.1556G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001406836.1:c.1460G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001406837.1:c.1286G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001406838.1:c.1016G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_181798.2:c.1175G>A - missense variant - [Sequence Ontology: SO:0001583]