ClinVar

NM_000218.3(KCNQ1):c.604G>A (p.Asp202Asn)

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: 2570754 (on Assembly GRCh38)
• Chr11: 2591984 (on Assembly GRCh37)

Preferred name:

NM_000218.3(KCNQ1):c.604G>A (p.Asp202Asn)

Other names:

p.D202N:GAC>AAC

HGVS:

• NC_000011.10:g.2570754G>A
• NG_008935.1:g.130764G>A
• NM_000218.3:c.604G>AMANE SELECT
• NM_001406836.1:c.604G>A
• NM_001406837.1:c.334G>A
• NM_181798.2:c.223G>A
• NP_000209.2:p.Asp202Asn
• NP_000209.2:p.Asp202Asn
• NP_001393765.1:p.Asp202Asn
• NP_001393766.1:p.Asp112Asn
• NP_861463.1:p.Asp75Asn
• NP_861463.1:p.Asp75Asn
• LRG_287t1:c.604G>A
• LRG_287t2:c.223G>A
• LRG_287:g.130764G>A
• LRG_287p1:p.Asp202Asn
• LRG_287p2:p.Asp75Asn
• NC_000011.9:g.2591984G>A
• NM_000218.2:c.604G>A
• NM_181798.1:c.223G>A
• NR_040711.2:n.497G>A

This HGVS expression did not pass validation

Protein change:

D112N

Links:

dbSNP: rs199472702

NCBI 1000 Genomes Browser:

rs199472702

Molecular consequence:

• NM_000218.3:c.604G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001406836.1:c.604G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001406837.1:c.334G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_181798.2:c.223G>A - missense variant - [Sequence Ontology: SO:0001583]