ClinVar

NM_001378969.1(KCND3):c.950G>A (p.Cys317Tyr)

Gene:

KCND3:potassium voltage-gated channel subfamily D member 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p13.2

Genomic location:

• Chr1: 111981777 (on Assembly GRCh38)
• Chr1: 112524399 (on Assembly GRCh37)

Preferred name:

NM_001378969.1(KCND3):c.950G>A (p.Cys317Tyr)

HGVS:

• NC_000001.11:g.111981777C>T
• NG_032011.2:g.12379G>A
• NM_001378969.1:c.950G>AMANE SELECT
• NM_001378970.1:c.950G>A
• NM_004980.5:c.950G>A
• NM_172198.3:c.950G>A
• NP_001365898.1:p.Cys317Tyr
• NP_001365899.1:p.Cys317Tyr
• NP_004971.2:p.Cys317Tyr
• NP_004971.2:p.Cys317Tyr
• NP_751948.1:p.Cys317Tyr
• LRG_445t1:c.950G>A
• LRG_445:g.12379G>A
• LRG_445p1:p.Cys317Tyr
• NC_000001.10:g.112524399C>T
• NM_004980.4:c.950G>A

This HGVS expression did not pass validation

Protein change:

C317Y

Links:

dbSNP: rs1571939905

NCBI 1000 Genomes Browser:

rs1571939905

Molecular consequence:

• NM_001378969.1:c.950G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001378970.1:c.950G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_004980.5:c.950G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_172198.3:c.950G>A - missense variant - [Sequence Ontology: SO:0001583]

Observations:

1