Transcript #00024060 (NM_002976.3, SCN7A gene)

Transcript name transcript variant 1
Gene name SCN7A (sodium channel, voltage gated, type VII alpha subunit)
Chromosome 2
Transcript - NCBI ID NM_002976.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_002967.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2015-09-27 11:53:03 +02:00 (CEST)
Date last edited N/A


Variants

129 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.146del r.(?) p.(Lys49SerfsTer33)
?/. - c.281C>T r.(?) p.(Ala94Val)
-?/. - c.301T>A r.(?) p.(Leu101Met)
-?/. - c.314A>G r.(?) p.(Asn105Ser)
-?/. - c.319A>G r.(?) p.(Ile107Val)
-?/. - c.353+6C>A r.(=) p.(=)
-?/. - c.528C>T r.(?) p.(Leu176=)
?/. - c.532G>A r.(?) p.(Asp178Asn)
-?/. - c.558C>T r.(?) p.(Ser186=)
?/. - c.559G>A r.(?) p.(Val187Ile)
-?/. - c.611C>T r.(?) p.(Thr204Met)
-?/. - c.612G>A r.(?) p.(Thr204=)
?/. - c.638T>G r.(?) p.(Ile213Ser)
-?/. - c.665-8C>T r.(=) p.(=)
-?/. - c.707A>C r.(?) p.(Gln236Pro)
-?/. - c.741T>C r.(?) p.(Phe247=)
?/. - c.757C>G r.(?) p.(Leu253Val)
+?/. - c.805C>T r.(?) p.(Arg269Ter)
-?/. - c.860A>G r.(?) p.(Tyr287Cys)
-?/. - c.872-19T>C r.(=) p.(=)
?/. - c.934G>A r.(?) p.(Asp312Asn)
-?/. - c.1003A>G r.(?) p.(Asn335Asp)
?/. - c.1043G>A r.(?) p.(Arg348Gln)
?/. - c.1046T>A r.(?) p.(Leu349Ter)
-?/. - c.1069G>A r.(?) p.(Val357Ile)
-?/. - c.1248A>G r.(?) p.(Gln416=)
-?/. - c.1248A>G r.(?) p.(Gln416=)
-?/. - c.1253C>A r.(?) p.(Thr418Asn)
-?/. - c.1290+6T>C r.(=) p.(=)
?/. - c.1300A>G r.(?) p.(Ile434Val)
-?/. - c.1317G>C r.(?) p.(Lys439Asn)
-?/. - c.1341C>T r.(?) p.(Asp447=)
-?/. - c.1348T>C r.(?) p.(Leu450=)
?/. - c.1364A>G r.(?) p.(Asp455Gly)
-?/. - c.1367C>G r.(?) p.(Ala456Gly)
-?/. - c.1374C>T r.(?) p.(Leu458=)
-?/. - c.1398A>G r.(?) p.(Lys466=)
-?/. - c.1407G>A r.(?) p.(Lys469=)
-?/. - c.1479A>G r.(?) p.(Lys493=)
-?/. - c.1501A>C r.(?) p.(Ile501Leu)
-?/. - c.1539A>G r.(?) p.(Ile513Met)
-?/. - c.1613A>G r.(?) p.(Asn538Ser)
?/. - c.1646C>T r.(?) p.(Thr549Ile)
-/. - c.1685A>G r.(?) p.(Tyr562Cys)
-/. - c.1685A>G r.(?) p.(Tyr562Cys)
-?/. - c.1798A>T r.(?) p.(Met600Leu)
-/. - c.1798A>T r.(?) p.(Met600Leu)
-?/. - c.1930T>A r.(?) p.(Phe644Ile)
-?/. - c.1932C>T r.(?) p.(Phe644=)
-?/. - c.1970T>C r.(?) p.(Val657Ala)
-?/. - c.1995A>G r.(?) p.(Gln665=)
-?/. - c.1996C>G r.(?) p.(Leu666Val)
?/. - c.2042T>C r.(?) p.(Val681Ala)
?/. - c.2047C>T r.(?) p.(Arg683Ter)
-?/. - c.2048G>A r.(?) p.(Arg683Gln)
-/. - c.2048G>A r.(?) p.(Arg683Gln)
-/. - c.2048G>A r.(?) p.(Arg683Gln)
+?/. - c.2081G>A r.(?) p.(Trp694Ter)
-?/. - c.2157+15C>A r.(=) p.(=)
-?/. - c.2157+19T>C r.(=) p.(=)
-?/. - c.2158-4T>G r.spl? p.?
?/. - c.2171T>G r.(?) p.(Phe724Cys)
-?/. - c.2204A>G r.(?) p.(Lys735Arg)
?/. - c.2257del r.(?) p.(Ala753GlnfsTer7)
-/. - c.2408A>T r.(?) p.(Asp803Val)
-?/. - c.2431A>G r.(?) p.(Ser811Gly)
-?/. - c.2452G>T r.(?) p.(Ala818Ser)
-?/. - c.2454T>C r.(?) p.(Ala818=)
-?/. - c.2477T>A r.(?) p.(Leu826His)
-?/. - c.2502A>T r.(?) p.(Glu834Asp)
-?/. - c.2541T>C r.(?) p.(Asn847=)
-?/. - c.2604A>G r.(?) p.(Gln868=)
-?/. - c.2699-5G>A r.spl? p.?
-?/. - c.2707C>T r.(?) p.(Arg903Cys)
-/. - c.2710G>A r.(?) p.(Gly904Arg)
-?/. - c.2720T>C r.(?) p.(Leu907Pro)
?/. - c.2795A>C r.(?) p.(Glu932Ala)
?/. - c.2867T>C r.(?) p.(Ile956Thr)
-?/. - c.3027+7A>G r.(=) p.(=)
-?/. - c.3028-9A>T r.(=) p.(=)
-/. - c.3028-9A>T r.(=) p.(=)
-?/. - c.3038T>G r.(?) p.(Leu1013Arg)
-?/. - c.3059G>A r.(?) p.(Arg1020Gln)
-?/. - c.3128G>A r.(?) p.(Arg1043Lys)
-?/. - c.3243T>C r.(?) p.(Ala1081=)
-?/. - c.3316C>T r.(?) p.(Arg1106Trp)
-?/. - c.3339C>T r.(?) p.(Asn1113=)
-?/. - c.3340G>A r.(?) p.(Glu1114Lys)
-?/. - c.3415-17G>A r.(=) p.(=)
?/. - c.3461C>A r.(?) p.(Ser1154Tyr)
?/. - c.3551_3554del r.(?) p.(Pro1184ArgfsTer4)
?/. - c.3610G>A r.(?) p.(Gly1204Arg)
-?/. - c.3630A>G r.(?) p.(Ile1210Met)
?/. - c.3664A>T r.(?) p.(Lys1222*)
-?/. - c.3712-12T>C r.(=) p.(=)
./. - c.3712-2A>G r.spl? p.?
-/. - c.3712-2A>G r.spl? p.?
-?/. - c.3735T>C r.(?) p.(Phe1245=)
-?/. - c.3787T>C r.(?) p.(Phe1263Leu)
?/. - c.3805A>G r.(?) p.(Met1269Val)
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