ClinVar

NM_001127222.2(CACNA1A):c.2606G>A (p.Arg869Gln)

Gene:

CACNA1A:calcium voltage-gated channel subunit alpha1 A [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19p13.13

Genomic location:

• Chr19: 13299027 (on Assembly GRCh38)
• Chr19: 13409841 (on Assembly GRCh37)

Preferred name:

NM_001127222.2(CACNA1A):c.2606G>A (p.Arg869Gln)

HGVS:

• NC_000019.10:g.13299027C>T
• NG_011569.1:g.212434G>A
• NM_000068.4:c.2618G>A
• NM_001127221.2:c.2609G>A
• NM_001127222.2:c.2606G>AMANE SELECT
• NM_001174080.2:c.2609G>A
• NM_023035.3:c.2618G>A
• NP_000059.3:p.Arg873Gln
• NP_001120693.1:p.Arg870Gln
• NP_001120693.1:p.Arg870Gln
• NP_001120694.1:p.Arg869Gln
• NP_001167551.1:p.Arg870Gln
• NP_075461.2:p.Arg873Gln
• LRG_7t1:c.2609G>A
• LRG_7:g.212434G>A
• LRG_7p1:p.Arg870Gln
• NC_000019.9:g.13409841C>T
• NM_001127221.1:c.2609G>A

This HGVS expression did not pass validation

Protein change:

R869Q

Links:

dbSNP: rs1057518589

NCBI 1000 Genomes Browser:

rs1057518589

Molecular consequence:

• NM_000068.4:c.2618G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001127221.2:c.2609G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001127222.2:c.2606G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001174080.2:c.2609G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_023035.3:c.2618G>A - missense variant - [Sequence Ontology: SO:0001583]