Transcript #00026668 (NM_001159575.1, SCNN1A gene)

Transcript name transcript variant 3
Gene name SCNN1A (sodium channel, non-voltage-gated 1 alpha subunit)
Chromosome 12
Transcript - NCBI ID NM_001159575.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001153047.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

89 entries on 1 page. Showing entries 1 - 89.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.168C>T 168 r.(?) p.(=) - coding-synonymous -
./. - c.195G>A 195 r.(?) p.(=) - coding-synonymous -
./. - c.610C>T 610 r.(?) p.(Arg204Trp) - missense -
./. - c.754-39C>T 754 r.(=) p.(=) - intron 39
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1069G>A 1069 r.(?) p.(Ala357Thr) - missense -
./. - c.1117C>T 1117 r.(?) p.(Arg373Trp) - missense -
./. - c.1429+47C>T 1429 r.(=) p.(=) - intron 47
./. - c.1496G>A 1496 r.(?) p.(Arg499Gln) - missense -
./. - c.1554G>T 1554 r.(?) p.(=) - coding-synonymous -
./. - c.1554G>T 1554 r.(?) p.(=) - coding-synonymous -
./. - c.1554G>T 1554 r.(?) p.(=) - coding-synonymous -
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1622+32G>A 1622 r.(=) p.(=) - intron 32
./. - c.1922G>T 1922 r.(?) p.(Cys641Phe) - missense -
./. - c.1922G>T 1922 r.(?) p.(Cys641Phe) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.2056A>G 2056 r.(?) p.(Thr686Ala) - missense -
./. - c.*76G>A 2155 r.(=) p.(=) - utr-3 -
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