ClinVar

NM_000335.5(SCN5A):c.5479G>A (p.Ala1827Thr)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

3p22.2

Genomic location:

• Chr3: 38550890 (on Assembly GRCh38)
• Chr3: 38592381 (on Assembly GRCh37)

Preferred name:

NM_000335.5(SCN5A):c.5479G>A (p.Ala1827Thr)

Other names:

p.A1828T:GCC>ACC

HGVS:

• NC_000003.12:g.38550890C>T
• NG_008934.1:g.103783G>A
• NM_000335.5:c.5479G>AMANE SELECT
• NM_001099404.2:c.5482G>A
• NM_001099405.2:c.5428G>A
• NM_001160160.2:c.5383G>A
• NM_001160161.2:c.5320G>A
• NM_001354701.2:c.5425G>A
• NM_198056.3:c.5482G>A
• NP_000326.2:p.Ala1827Thr
• NP_001092874.1:p.Ala1828Thr
• NP_001092875.1:p.Ala1810Thr
• NP_001153632.1:p.Ala1795Thr
• NP_001153633.1:p.Ala1774Thr
• NP_001341630.1:p.Ala1809Thr
• NP_932173.1:p.Ala1828Thr
• NP_932173.1:p.Ala1828Thr
• LRG_289t1:c.5482G>A
• LRG_289:g.103783G>A
• LRG_289p1:p.Ala1828Thr
• NC_000003.11:g.38592381C>T
• NM_001099404.1:c.5482G>A
• NM_198056.2:c.5482G>A

This HGVS expression did not pass validation

Protein change:

A1774T

Links:

dbSNP: rs774593360

NCBI 1000 Genomes Browser:

rs774593360

Molecular consequence:

• NM_000335.5:c.5479G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001099404.2:c.5482G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001099405.2:c.5428G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001160160.2:c.5383G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001160161.2:c.5320G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_001354701.2:c.5425G>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_198056.3:c.5482G>A - missense variant - [Sequence Ontology: SO:0001583]