ClinVar

NM_001330260.2(SCN8A):c.5719C>T (p.Arg1907Trp)

Gene:

SCN8A:sodium voltage-gated channel alpha subunit 8 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

12q13.13

Genomic location:

• Chr12: 51807205 (on Assembly GRCh38)
• Chr12: 52200989 (on Assembly GRCh37)

Preferred name:

NM_001330260.2(SCN8A):c.5719C>T (p.Arg1907Trp)

HGVS:

• NC_000012.12:g.51807205C>T
• NG_021180.3:g.222248C>T
• NM_001177984.3:c.5596C>T
• NM_001330260.2:c.5719C>TMANE SELECT
• NM_001369788.1:c.5596C>T
• NM_014191.4:c.5719C>T
• NP_001171455.1:p.Arg1866Trp
• NP_001317189.1:p.Arg1907Trp
• NP_001356717.1:p.Arg1866Trp
• NP_055006.1:p.Arg1907Trp
• LRG_1389t1:c.5719C>T
• LRG_1389t2:c.5719C>T
• LRG_1389:g.222248C>T
• LRG_1389p1:p.Arg1907Trp
• LRG_1389p2:p.Arg1907Trp
• NC_000012.11:g.52200989C>T
• NM_014191.3:c.5719C>T

This HGVS expression did not pass validation

Protein change:

R1866W

Links:

dbSNP: rs760444517

NCBI 1000 Genomes Browser:

rs760444517

Molecular consequence:

• NM_001177984.3:c.5596C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001330260.2:c.5719C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001369788.1:c.5596C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_014191.4:c.5719C>T - missense variant - [Sequence Ontology: SO:0001583]

Observations:

1