Transcript #00001497 (NM_001003406.1, CACNA1I gene)

Transcript name transcript variant 2
Gene name CACNA1I (calcium channel, voltage-dependent, T type, alpha 1I subunit)
Chromosome 22
Transcript - NCBI ID NM_001003406.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001003406.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-09-13 13:36:23 +02:00 (CEST)
Date last edited N/A


Variants

64 entries on 1 page. Showing entries 1 - 64.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.349-1050T>G r.(=) p.(=)
?/. - c.452A>G r.(?) p.(Asn151Ser)
?/. - c.533G>T r.(?) p.(Arg178Leu)
-?/. - c.816G>A r.(?) p.(=)
-?/. - c.898G>A r.(?) p.(Val300Ile)
-?/. - c.914C>T r.(?) p.(Ala305Val)
-?/. - c.920G>A r.(?) p.(Arg307His)
?/. - c.1193C>A r.(?) p.(Ala398Glu)
?/. - c.1193C>T r.(?) p.(Ala398Val)
?/. - c.1193C>T r.(?) p.(Ala398Val)
-?/. - c.1313T>C r.(?) p.(Ile438Thr)
-?/. - c.1355G>A r.(?) p.(Arg452His)
-?/. - c.1450C>T r.(?) p.(Pro484Ser)
-?/. - c.1508T>C r.(?) p.(Leu503Pro)
-?/. - c.1525G>A r.(?) p.(Ala509Thr)
-?/. - c.1610C>T r.(?) p.(Ser537Leu)
?/. - c.1657G>A r.(?) p.(Glu553Lys)
?/. - c.1711G>A r.(?) p.(Gly571Arg)
?/. - c.1732_1734dup r.(?) p.(Glu578dup)
?/. - c.1771T>C r.(?) p.(Trp591Arg)
?/. - c.1825C>T r.(?) p.(Arg609Trp)
-?/. - c.1939A>G r.(?) p.(Met647Val)
-?/. - c.2067C>T r.(?) p.(Asp689=)
?/. - c.2267G>A r.(?) p.(Arg756His)
?/. - c.2270C>T r.(?) p.(Thr757Met)
-?/. - c.2293G>A r.(?) p.(Asp765Asn)
+?/. - c.2475C>G r.(?) p.(Ile825Met)
-?/. - c.2513G>A r.(?) p.(Arg838His)
-?/. - c.2689C>A r.(?) p.(Pro897Thr)
-?/. - c.2714C>T r.(?) p.(Pro905Leu)
-?/. - c.2744G>A r.(?) p.(Arg915Gln)
?/. - c.3041G>A r.(?) p.(Arg1014His)
?/. - c.3041_3042delinsAA r.(?) p.(Arg1014Gln)
-?/. - c.3259A>G r.(?) p.(Ile1087Val)
?/. - c.3291G>C r.(?) p.(Lys1097Asn)
-?/. - c.3369-7_3369-6del r.(=) p.(=)
-?/. - c.3369-6G>C r.(=) p.(=)
-?/. - c.3369-2_3371del r.spl? p.?
?/. - c.3492+4A>G r.spl? p.?
-?/. - c.3562-10C>A r.(=) p.(=)
-?/. - c.3909G>C r.(?) p.(Val1303=)
?/. - c.3932G>A r.(?) p.(Arg1311His)
?/. - c.3944T>C r.(?) p.(Met1315Thr)
?/. - c.4130T>C r.(?) p.(Ile1377Thr)
-?/. - c.4279C>T r.(?) p.(Arg1427Trp)
-?/. - c.4280G>A r.(?) p.(Arg1427Gln)
?/. - c.4291C>T r.(?) p.(Arg1431Trp)
-?/. - c.4498G>T r.(?) p.(Val1500Leu)
?/. - c.4640C>T r.(?) p.(Thr1547Ile)
-?/. - c.4679-5C>T r.spl? p.?
?/. - c.4749+604C>G r.(=) p.(=)
?/. - c.4749+716_4749+719dup r.(=) p.(=)
?/. - c.4939G>A r.(?) p.(Gly1647Arg)
?/. - c.5201C>T r.(?) p.(Pro1734Leu)
?/. - c.5215C>T r.(?) p.(Arg1739*)
?/. - c.5330A>G r.(?) p.(Asp1777Gly)
?/. - c.5354T>A r.(?) p.(Ile1785Asn)
-?/. - c.5642C>T r.(?) p.(Pro1881Leu)
-?/. - c.5748G>A r.(?) p.(=)
?/. - c.5969C>T r.(?) p.(Ala1990Val)
?/. - c.6013G>T r.(?) p.(Asp2005Tyr)
-?/. - c.6141G>A r.(?) p.(=)
-?/. - c.6188C>T r.(?) p.(Thr2063Ile)
?/. - c.6334C>A r.(?) p.(Leu2112Ile)
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