Transcript #00024130 (NM_001168272.1, ITPR1 gene)

Transcript name transcript variant 3
Gene name ITPR1 (inositol 1,4,5-trisphosphate receptor, type 1)
Chromosome 3
Transcript - NCBI ID NM_001168272.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001161744.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2016-05-12 21:45:40 +02:00 (CEST)
Date last edited N/A


Variants

288 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. _1_47i c.-59670_6246+1060del r.0 p.0
+/. _1_47i c.-59670_6246+1060del r.0 p.0
+/. _1_10i c.-47374_855+2104del r.0 p.0
+/. - c.(-38551_-34358)_(*24418_*24782)del r.0 p.0
+/. _1_51i c.-13100_6764-1150del r.0 p.0
?/. - c.-8del r.(?) p.(=)
?/. 36 c.? r.? p.?
?/. 47 c.? r.? p.?
?/. 45 c.? r.? p.?
-?/. - c.66G>A r.(?) p.(=)
+?/. - c.100G>A r.(?) p.(Asp34Asn)
+/. - c.106C>T r.(?) p.(Arg36Cys)
?/. - c.178C>G r.(?) p.(Leu60Val)
?/. - c.200C>T r.(?) p.(Ser67Phe)
+/. - c.239C>A r.(?) p.(Ala80Asp)
-?/. - c.280-10C>A r.(=) p.(=)
?/. - c.356A>G r.(?) p.(Asn119Ser)
-/. - c.438C>T r.(?) p.(Ala146=)
-?/. - c.525+9G>A r.(=) p.(=)
-?/. - c.624+18T>C r.(=) p.(=)
-?/. - c.624+18T>C r.(=) p.(=)
+?/. - c.722G>A r.(?) p.(Arg241Lys)
+/. - c.722G>A r.(?) p.(Arg241Lys)
+?/. - c.727T>G r.(?) p.(Phe243Val)
?/. - c.742_744del r.(?) p.(Glu248del)
+?/. - c.748T>C r.(?) p.(Phe250Leu)
?/. - c.750T>G r.(?) p.(Phe250Leu)
?/. 10 c.755C>T r.(?) p.(Thr252Ile)
?/. - c.773A>T r.(?) p.(Lys258Met)
?/. - c.784G>A r.(?) p.(Val262Ile)
+/. 10 c.799A>G r.(?) p.(Thr267Ala)
+/. - c.800C>G r.(?) p.(Thr267Arg)
+/. - c.800C>T r.(?) p.(Thr267Met)
+/. - c.805C>T r.(?) p.(Arg269Trp)
+?/. - c.805C>T r.(?) p.(Arg269Trp)
+/. - c.805C>T r.(?) p.(Arg269Trp)
+/. 10 c.805C>T r.(?) p.(Arg269Trp)
+?/. - c.805C>T r.(?) p.(Arg269Trp)
+/. - c.830G>T r.(?) p.(Ser277Ile)
+?/. - c.830G>T r.(?) p.(Ser277Ile)
-?/. - c.855+18A>G r.(=) p.(=)
?/. - c.877C>T r.(?) p.(Arg293Trp)
?/. - c.902G>C r.(?) p.(Ser301Thr)
-?/. - c.970G>A r.(?) p.(Ala324Thr)
?/. - c.970G>A r.(?) p.(Ala324Thr)
?/. - c.988C>T r.(?) p.(Arg330Trp)
?/. - c.988C>T r.(?) p.(Arg330Trp)
?/. - c.1042G>A r.(?) p.(Asp348Asn)
-/. - c.1080G>A r.(?) p.(Leu360=)
-/. - c.1080G>A r.(?) p.(Leu360=)
-?/. - c.1101C>A r.(?) p.(Val367=)
-/. - c.1106+5C>G r.spl? p.?
?/. - c.1150G>T r.(?) p.(Val384Phe)
-/. - c.1206+10G>A r.(=) p.(=)
-/. - c.1257G>A r.(?) p.(Pro419=)
-/. - c.1367+11C>T r.(=) p.(=)
-/. - c.1367+13G>A r.(=) p.(=)
-?/. - c.1368-18_1368-16del r.(=) p.(=)
?/. - c.1373T>C r.(?) p.(Val458Ala)
-?/. - c.1435G>A r.(?) p.(Val479Ile)
-?/. - c.1435G>A r.(?) p.(Val479Ile)
-/. - c.1435G>A r.(?) p.(Val479Ile)
-?/. - c.1435G>A r.(?) p.(Val479Ile)
?/. 15 c.1447G>A r.(?) p.(Val483Ile)
?/. - c.1462A>G r.(?) p.(Asn488Asp)
?/. - c.1471C>T r.(?) p.(Arg491Trp)
+/. - c.1489G>A r.(?) p.(Glu497Lys)
-/. - c.1491A>G r.(?) p.(Glu497=)
-?/. - c.1509+3C>T r.spl? p.?
-?/. - c.1509+6T>G r.(=) p.(=)
-?/. - c.1509+9G>A r.(=) p.(=)
-/. - c.1509+17G>A r.(=) p.(=)
+/. - c.1645C>T r.(?) p.(Gln549*)
?/. - c.1679C>A r.(?) p.(Ala560Asp)
+/. - c.1736C>T r.(?) p.(Thr579Ile)
+/. - c.1759A>G r.(?) p.(Asn587Asp)
+/. - c.1759A>G r.(?) p.(Asn587Asp)
?/. - c.1822C>A r.(?) p.(=)
-?/. - c.1881C>T r.(?) p.(Asn627=)
-?/. - c.1962-3T>C r.spl? p.?
-?/. - c.1962-3T>C r.spl? p.?
-?/. - c.1962-3T>C r.spl? p.?
-?/. - c.1962-3T>C r.spl? p.?
-/. - c.1962G>A r.(?) p.(Lys654=)
?/. - c.2009A>G r.(?) p.(Glu670Gly)
?/. - c.2009A>G r.(?) p.(Glu670Gly)
+/. - c.2049G>A r.(?) p.(Trp683Ter)
-?/. - c.2066G>C r.(?) p.(Ser689Thr)
?/. - c.2074G>A r.(?) p.(Glu692Lys)
?/. - c.2080C>T r.(?) p.(Arg694Cys)
+/. 19 c.2137C>T r.(?) p.(Arg713*)
-?/. - c.2159+3G>A r.spl? p.?
-/. - c.2159+13C>T r.(=) p.(=)
+?/. - c.2180C>T r.(?) p.(Ala727Val)
-?/. - c.2181G>A r.(?) p.(Ala727=)
-?/. - c.2181G>A r.(?) p.(Ala727=)
?/. - c.2197C>T r.(?) p.(Arg733Cys)
-?/. - c.2235G>T r.(?) p.(Leu745=)
-?/. - c.2260A>G r.(?) p.(Met754Val)
-/. - c.2260A>G r.(?) p.(Met754Val)
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