ClinVar

NM_000525.4(KCNJ11):c.941G>A (p.Arg314His)

Gene:

KCNJ11:potassium inwardly rectifying channel subfamily J member 11 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

11p15.1

Genomic location:

• Chr11: 17387151 (on Assembly GRCh38)
• Chr11: 17408698 (on Assembly GRCh37)

Preferred name:

NM_000525.4(KCNJ11):c.941G>A (p.Arg314His)

HGVS:

• NC_000011.10:g.17387151C>T
• NG_012446.1:g.6509G>A
• NM_000525.4:c.941G>AMANE SELECT
• NM_001166290.2:c.680G>A
• NM_001377296.1:c.680G>A
• NM_001377297.1:c.680G>A
• NP_000516.3:p.Arg314His
• NP_001159762.1:p.Arg227His
• NP_001364225.1:p.Arg227His
• NP_001364226.1:p.Arg227His
• NC_000011.9:g.17408698C>T
• NM_000525.3:c.941G>A

This HGVS expression did not pass validation

Protein change:

R227H

Links:

dbSNP: rs145935651

NCBI 1000 Genomes Browser:

rs145935651

Molecular consequence:

• NM_000525.4:c.941G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001166290.2:c.680G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001377296.1:c.680G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001377297.1:c.680G>A - missense variant - [Sequence Ontology: SO:0001583]