Transcript #00018530 (NM_000336.2, SCNN1B gene)

Transcript name sodium channel, nonvoltage-gated 1, beta
Gene name SCNN1B (sodium channel, non-voltage-gated 1, beta subunit)
Chromosome 16
Transcript - NCBI ID NM_000336.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000327.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

68 entries on 1 page. Showing entries 1 - 68.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-1783560_*5940123del r.0? p.0?
-?/. - c.6C>T r.(?) p.(His2=)
+/. - c.84G>A r.(?) p.(Trp28Ter)
+/. 2 c.87C>A r.(?) p.(Tyr29*)
+/. 2 c.109G>A r.(?) p.(Gly37Ser)
-?/. - c.245C>G r.(?) p.(Ser82Cys)
-?/. - c.245C>G r.(?) p.(Ser82Cys)
?/? 2 c.245C>G r.(?) p.(Ser82Cys)
-/. - c.279T>C r.(?) p.(Pro93=)
?/? 2 c.279T>C r.(?) p.(=)
-/. - c.279T>C r.(?) p.(Pro93=)
-?/. - c.282C>T r.(?) p.(=)
-?/. - c.466C>T r.(?) p.(Arg156Trp)
+/. 3 c.520_521insA r.(?) p.(Leu174Tyrfs*12)
+/. 4 c.637C>T r.(?) p.(Gln213*)
+/. 4 c.648dup r.(?) p.(Glu217Argfs*38)
-/. - c.777-42C>T r.(=) p.(=)
?/? 4i c.777-5T>C r.(?) p.(?)
+/. 5 c.789del r.(?) p.(Ile264Serfs*16)
?/? 5 c.879C>T r.(?) p.(=)
-/. - c.879C>T r.(?) p.(Phe293=)
+/. 6 c.915del r.(?) p.(Tyr306Thrfs*13)
-?/. - c.1005C>T r.(?) p.(Tyr335=)
?/? 6 c.1042G>A r.(?) p.(Val348Met)
?/. - c.1105C>A r.(?) p.(Pro369Thr)
?/. - c.1108G>A r.(?) p.(Val370Ile)
-/. - c.1162C>T r.(?) p.(Arg388Cys)
-?/. - c.1229G>A r.(?) p.(Arg410His)
+/. 8 c.1245dup r.(?) p.(Asn416Glnfs*35)
-?/. - c.1270+14C>T r.(=) p.(=)
+/. - c.1271-1G>C r.spl p.?
+/. 9 c.1288del r.(?) p.(Leu430Tyrfs*3)
-?/. - c.1313A>G r.(?) p.(Glu438Gly)
?/? 9 c.1325G>T r.(?) p.(Gly442Val)
+/. - c.1346+1G>A r.spl p.?
?/? 9i c.1346+28C>T r.(?) p.(?)
-?/. - c.1435C>T r.(?) p.(Arg479Trp)
+/. - c.1466+1G>A r.spl p.?
-/. - c.1467-14G>A r.(=) p.(=)
-/. - c.1467-14G>A r.(=) p.(=)
+/. - c.1542+1G>A r.spl p.?
+/. - c.1542+1G>A r.spl p.?
+/. - c.1542+1G>A r.spl p.?
-?/. - c.1542+17C>T r.(=) p.(=)
-/. - c.1543-17C>T r.(=) p.(=)
-?/. - c.1545C>T r.(?) p.(Ile515=)
-?/. - c.1545C>T r.(?) p.(Ile515=)
?/? 13 c.1545C>T r.(?) p.(=)
+/. 13 c.1636G>A r.(?) p.(Asp546Asn)
+/. - c.1696C>T r.(?) p.(Arg566*)
-?/. - c.1706C>T r.(?) p.(Ala569Val)
-?/. - c.1731C>T r.(?) p.(Thr577=)
?/? 13 c.1731C>T r.(?) p.(=)
-?/. - c.1765G>A r.(?) p.(Gly589Ser)
-?/. - c.1765G>A r.(?) p.(Gly589Ser)
?/? 13 c.1765G>A r.(?) p.(Gly589Ser)
?/? 13 c.1781C>T r.(?) p.(Thr594Met)
-?/. - c.1782G>A r.(?) p.(Thr594=)
+/. - c.1847C>T r.(?) p.(Pro616Leu)
+/. - c.1849C>T r.(?) p.(Pro617Ser)
+/. - c.1853C>A r.(?) p.(Pro618His)
?/. - c.1870C>T r.(?) p.(Arg624Cys)
-?/. - c.1883T>A r.(?) p.(Leu628Gln)
-?/. - c.1887C>T r.(?) p.(Asp629=)
?/? 13 c.1887C>T r.(?) p.(=)
-?/. - c.1888G>A r.(?) p.(Val630Ile)
-?/. - c.1888G>A r.(?) p.(Val630Ile)
-?/. - c.1893C>T r.(?) p.(=)
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