ClinVar

NM_000335.5(SCN5A):c.5208C>T (p.Gly1736=)

Gene:

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

Variant type:

single nucleotide variant

Cytogenetic location:

3p22.2

Genomic location:

• Chr3: 38551161 (on Assembly GRCh38)
• Chr3: 38592652 (on Assembly GRCh37)

Preferred name:

NM_000335.5(SCN5A):c.5208C>T (p.Gly1736=)

HGVS:

• NC_000003.12:g.38551161G>A
• NG_008934.1:g.103512C>T
• NM_000335.5:c.5208C>TMANE SELECT
• NM_001099404.2:c.5211C>T
• NM_001099405.2:c.5157C>T
• NM_001160160.2:c.5112C>T
• NM_001160161.2:c.5049C>T
• NM_001354701.2:c.5154C>T
• NM_198056.3:c.5211C>T
• NP_000326.2:p.Gly1736=
• NP_000326.2:p.Gly1736=
• NP_001092874.1:p.Gly1737=
• NP_001092874.1:p.Gly1737=
• NP_001092875.1:p.Gly1719=
• NP_001153632.1:p.Gly1704=
• NP_001153633.1:p.Gly1683=
• NP_001341630.1:p.Gly1718=
• NP_932173.1:p.Gly1737=
• NP_932173.1:p.Gly1737=
• LRG_289t1:c.5211C>T
• LRG_289t2:c.5208C>T
• LRG_289t3:c.5211C>T
• LRG_289:g.103512C>T
• LRG_289p1:p.Gly1737=
• LRG_289p2:p.Gly1736=
• LRG_289p3:p.Gly1737=
• NC_000003.11:g.38592652G>A
• NM_000335.4:c.5208C>T
• NM_001099404.1:c.5211C>T
• NM_198056.2:c.5211C>T
• NR_176299.1:n.5957C>T

This HGVS expression did not pass validation

Molecular consequence:

• NR_176299.1:n.5957C>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]
• NM_000335.5:c.5208C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001099404.2:c.5211C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001099405.2:c.5157C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001160160.2:c.5112C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001160161.2:c.5049C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_001354701.2:c.5154C>T - synonymous variant - [Sequence Ontology: SO:0001819]
• NM_198056.3:c.5211C>T - synonymous variant - [Sequence Ontology: SO:0001819]