ClinVar

NM_000335.5(SCN5A):c.1698C>T (p.Pro566=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

3p22.2

Genomic location:

• Chr3: 38603904 (on Assembly GRCh38)
• Chr3: 38645395 (on Assembly GRCh37)

Preferred name:

NM_000335.5(SCN5A):c.1698C>T (p.Pro566=)

HGVS:

• NC_000003.12:g.38603904G>A
• NG_008934.1:g.50769C>T
• NM_000335.5:c.1698C>TMANE SELECT
• NM_001099404.2:c.1698C>T
• NM_001099405.2:c.1698C>T
• NM_001160160.2:c.1698C>T
• NM_001160161.2:c.1698C>T
• NM_001354701.2:c.1698C>T
• NM_001407185.1:c.1698C>T
• NM_198056.3:c.1698C>T
• NP_000326.2:p.Pro566=
• NP_000326.2:p.Pro566=
• NP_001092874.1:p.Pro566=
• NP_001092874.1:p.Pro566=
• NP_001092875.1:p.Pro566=
• NP_001153632.1:p.Pro566=
• NP_001153633.1:p.Pro566=
• NP_001341630.1:p.Pro566=
• NP_001394114.1:p.Pro566=
• NP_932173.1:p.Pro566=
• NP_932173.1:p.Pro566=
• LRG_289t1:c.1698C>T
• LRG_289t2:c.1698C>T
• LRG_289t3:c.1698C>T
• LRG_289:g.50769C>T
• LRG_289p1:p.Pro566=
• LRG_289p2:p.Pro566=
• LRG_289p3:p.Pro566=
• NC_000003.11:g.38645395G>A
• NM_000335.4:c.1698C>T
• NM_001099404.1:c.1698C>T
• NM_198056.2:c.1698C>T
• NR_176299.1:n.2444C>T

This HGVS expression did not pass validation

Molecular consequence:

• NR_176299.1:n.2444C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_000335.5:c.1698C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001099404.2:c.1698C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001099405.2:c.1698C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001160160.2:c.1698C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001160161.2:c.1698C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001354701.2:c.1698C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001407185.1:c.1698C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_198056.3:c.1698C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Observations:

1