Colon Cancer: Gene >> ITPR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33677580:33677580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3599T>C
AA Mutation	p.Met1200Thr(p.M1200T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33663822:33663822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749099428
CDS Mutation	c.1090G>A
AA Mutation	p.Ala364Thr(p.A364T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33695051:33695051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7913A>G
AA Mutation	p.His2638Arg(p.H2638R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33683305:33683305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4696G>A
AA Mutation	p.Ala1566Thr(p.A1566T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33665151:33665151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1347C>A
AA Mutation	p.Ser449Arg(p.S449R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33688350:33688350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6487G>A
AA Mutation	p.Glu2163Lys(p.E2163K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33664875:33664875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753753894
CDS Mutation	c.1154C>T
AA Mutation	p.Ser385Leu(p.S385L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33692839:33692839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7570C>T
AA Mutation	p.Arg2524Cys(p.R2524C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33668567:33668567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142075453
CDS Mutation	c.1939G>A
AA Mutation	p.Val647Ile(p.V647I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33662625:33662625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777019225
CDS Mutation	c.809G>A
AA Mutation	p.Arg270His(p.R270H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33658725:33658725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.425T>C
AA Mutation	p.Leu142Ser(p.L142S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33680562:33680562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4358G>A
AA Mutation	p.Ser1453Asn(p.S1453N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33686105:33686105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5720C>T
AA Mutation	p.Thr1907Met(p.T1907M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33686185:33686185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778613128
CDS Mutation	c.5800G>A
AA Mutation	p.Val1934Met(p.V1934M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33683284:33683284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4675G>A
AA Mutation	p.Ala1559Thr(p.A1559T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33680636:33680636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763726545
CDS Mutation	c.4432G>A
AA Mutation	p.Ala1478Thr(p.A1478T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33688323:33688323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142820127
CDS Mutation	c.6460C>T
AA Mutation	p.Arg2154Trp(p.R2154W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33655769:33655769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.164G>T
AA Mutation	p.Cys55Phe(p.C55F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33668555:33668555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1927A>T
AA Mutation	p.Ile643Phe(p.I643F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33670530:33670530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767435428
CDS Mutation	c.2395T>C
AA Mutation	p.Phe799Leu(p.F799L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33663804:33663804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1072C>T
AA Mutation	p.Pro358Ser(p.P358S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33670404:33670404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2269G>A
AA Mutation	p.Val757Met(p.V757M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33675732:33675732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770956589
CDS Mutation	c.3158G>A
AA Mutation	p.Arg1053His(p.R1053H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33676915:33676915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3430G>A
AA Mutation	p.Ala1144Thr(p.A1144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33682588:33682588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4541T>C
AA Mutation	p.Leu1514Pro(p.L1514P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33665882:33665882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1457T>C
AA Mutation	p.Val486Ala(p.V486A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33680375:33680375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4271C>T
AA Mutation	p.Thr1424Met(p.T1424M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33662932:33662932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880C>T
AA Mutation	p.Arg294Cys(p.R294C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33684800:33684800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756479384
CDS Mutation	c.5164G>A
AA Mutation	p.Ala1722Thr(p.A1722T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33692791:33692791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7522G>A
AA Mutation	p.Val2508Met(p.V2508M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33692830:33692830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7561G>A
AA Mutation	p.Ala2521Thr(p.A2521T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33670522:33670522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762693746
CDS Mutation	c.2387C>T
AA Mutation	p.Pro796Leu(p.P796L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33680038:33680038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4129G>A
AA Mutation	p.Glu1377Lys(p.E1377K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33684634:33684634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5083C>A
AA Mutation	p.Leu1695Ile(p.L1695I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33687527:33687527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6227G>A
AA Mutation	p.Arg2076His(p.R2076H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33669073:33669073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2106G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33658813:33658813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33686435:33686435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5895T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33672183:33672183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2883C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33680028:33680028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758747831
CDS Mutation	c.4119C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33663872:33663872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372786080
CDS Mutation	c.1140C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33655794:33655794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.189C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33677053:33677053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3486G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33687231:33687231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766466833
CDS Mutation	c.6081C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33682610:33682610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571319160
CDS Mutation	c.4563C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33677516:33677516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3535C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33686145:33686145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202114409
CDS Mutation	c.5760C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33662584:33662584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.768G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33680614:33680614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771140880
CDS Mutation	c.4410C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	50
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374316
Start	33667164:33667164(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1592delG
AA Mutation	p.Gly531ValfsTer50(p.G531Vfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	51
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374316
Start	33667898:33667898(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1823delA
AA Mutation	p.Lys608SerfsTer66(p.K608Sfs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	52
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374316
Start	33694944:33694944(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7810delC
AA Mutation	p.Arg2604GlyfsTer30(p.R2604Gfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	53
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374316
Start	33684872:33684872(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5237delA
AA Mutation	p.Asn1746ThrfsTer30(p.N1746Tfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	54
Mutation Consequence	stop_gained
Transcription ID	ENST00000374316
Start	33676852:33676852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3367A>T
AA Mutation	p.Lys1123Ter(p.K1123*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	55
Mutation Consequence	stop_gained
Transcription ID	ENST00000374316
Start	33662612:33662612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747619884
CDS Mutation	c.796C>T
AA Mutation	p.Arg266Ter(p.R266*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ITPR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374316
Start	33676912:33676912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373241450
CDS Mutation	c.3427G>A
AA Mutation	p.Ala1143Thr(p.A1143T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33691075:33691075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7191C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374316
Start	33691090:33691090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751450550
CDS Mutation	c.7206G>T
Mutation Classification	Silent
Feature Type	Transcript