ClinVar

NM_000335.5(SCN5A):c.4168G>A (p.Gly1390Arg)

Gene:

SCN5A:sodium voltage-gated channel alpha subunit 5 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

3p22.2

Genomic location:

• Chr3: 38560221 (on Assembly GRCh38)
• Chr3: 38601712 (on Assembly GRCh37)

Preferred name:

NM_000335.5(SCN5A):c.4168G>A (p.Gly1390Arg)

Other names:

p.G1391R:GGA>AGA

HGVS:

• NC_000003.12:g.38560221C>T
• NG_008934.1:g.94452G>A
• NM_000335.5:c.4168G>AMANE SELECT
• NM_001099404.1:c.4171G>A
• NM_001099404.2:c.4171G>A
• NM_001099405.2:c.4171G>A
• NM_001160160.2:c.4168G>A
• NM_001160161.2:c.4009G>A
• NM_001354701.2:c.4168G>A
• NM_198056.3:c.4171G>A
• NP_000326.2:p.Gly1390Arg
• NP_001092874.1:p.Gly1391Arg
• NP_001092875.1:p.Gly1391Arg
• NP_001153632.1:p.Gly1390Arg
• NP_001153633.1:p.Gly1337Arg
• NP_001341630.1:p.Gly1390Arg
• NP_932173.1:p.Gly1391Arg
• NP_932173.1:p.Gly1391Arg
• LRG_289t1:c.4171G>A
• LRG_289t3:c.4171G>A
• LRG_289:g.94452G>A
• LRG_289p1:p.Gly1391Arg
• NC_000003.11:g.38601712C>T
• NM_198056.2:c.4171G>A
• NM_198056.3:c.4171G>A

This HGVS expression did not pass validation

Protein change:

G1337R

Links:

dbSNP: rs780405533

NCBI 1000 Genomes Browser:

rs780405533

Molecular consequence:

• NM_000335.5:c.4168G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001099404.2:c.4171G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001099405.2:c.4171G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001160160.2:c.4168G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001160161.2:c.4009G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001354701.2:c.4168G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_198056.3:c.4171G>A - missense variant - [Sequence Ontology: SO:0001583]