ClinVar

NM_000540.3(RYR1):c.5009G>A (p.Arg1670His)

Gene:

RYR1:ryanodine receptor 1 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

19q13.2

Genomic location:

• Chr19: 38485664 (on Assembly GRCh38)
• Chr19: 38976304 (on Assembly GRCh37)

Preferred name:

NM_000540.3(RYR1):c.5009G>A (p.Arg1670His)

HGVS:

• NC_000019.10:g.38485664G>A
• NG_008866.1:g.56965G>A
• NM_000540.3:c.5009G>AMANE SELECT
• NM_001042723.2:c.5009G>A
• NP_000531.2:p.Arg1670His
• NP_000531.2:p.Arg1670His
• NP_001036188.1:p.Arg1670His
• LRG_766t1:c.5009G>A
• LRG_766:g.56965G>A
• LRG_766p1:p.Arg1670His
• NC_000019.9:g.38976304G>A
• NM_000540.2:c.5009G>A

This HGVS expression did not pass validation

Protein change:

R1670H

Links:

dbSNP: rs1248039154

NCBI 1000 Genomes Browser:

rs1248039154

Molecular consequence:

• NM_000540.3:c.5009G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001042723.2:c.5009G>A - missense variant - [Sequence Ontology: SO:0001583]

Observations:

1