ClinVar

NM_000335.5(SCN5A):c.3890C>T (p.Pro1297Leu)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

3p22.2

Genomic location:

• Chr3: 38562485 (on Assembly GRCh38)
• Chr3: 38603976 (on Assembly GRCh37)

Preferred name:

NM_000335.5(SCN5A):c.3890C>T (p.Pro1297Leu)

HGVS:

• NC_000003.12:g.38562485G>A
• NG_008934.1:g.92188C>T
• NM_000335.5:c.3890C>TMANE SELECT
• NM_001099404.2:c.3893C>T
• NM_001099405.2:c.3893C>T
• NM_001160160.2:c.3890C>T
• NM_001160161.2:c.3731C>T
• NM_001354701.2:c.3890C>T
• NM_198056.3:c.3893C>T
• NP_000326.2:p.Pro1297Leu
• NP_001092874.1:p.Pro1298Leu
• NP_001092875.1:p.Pro1298Leu
• NP_001153632.1:p.Pro1297Leu
• NP_001153633.1:p.Pro1244Leu
• NP_001341630.1:p.Pro1297Leu
• NP_932173.1:p.Pro1298Leu
• NP_932173.1:p.Pro1298Leu
• LRG_289t1:c.3893C>T
• LRG_289:g.92188C>T
• LRG_289p1:p.Pro1298Leu
• NC_000003.11:g.38603976G>A
• NM_198056.2:c.3893C>T

This HGVS expression did not pass validation

Protein change:

P1244L; PRO1298LEU

Links:

OMIM: 600163.0025; dbSNP: rs28937319

NCBI 1000 Genomes Browser:

rs28937319

Molecular consequence:

• NM_000335.5:c.3890C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001099404.2:c.3893C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001099405.2:c.3893C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001160160.2:c.3890C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001160161.2:c.3731C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001354701.2:c.3890C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_198056.3:c.3893C>T - missense variant - [Sequence Ontology: SO:0001583]