Colon Cancer: Gene >> CIC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42290774:42290774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2006C>T
AA Mutation	p.Ala669Val(p.A669V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42292131:42292131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2932G>A
AA Mutation	p.Val978Met(p.V978M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42292647:42292647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3257C>T
AA Mutation	p.Ala1086Val(p.A1086V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42291260:42291260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2492C>T
AA Mutation	p.Thr831Met(p.T831M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42294937:42294937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770660004
CDS Mutation	c.4573A>G
AA Mutation	p.Thr1525Ala(p.T1525A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42292692:42292692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3302C>T
AA Mutation	p.Ala1101Val(p.A1101V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42292448:42292448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3157G>A
AA Mutation	p.Val1053Met(p.V1053M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42288908:42288908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376580917
CDS Mutation	c.952G>A
AA Mutation	p.Val318Ile(p.V318I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42294908:42294908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4544G>A
AA Mutation	p.Arg1515His(p.R1515H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42287696:42287696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.734A>C
AA Mutation	p.Glu245Ala(p.E245A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42290534:42290534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202152564
CDS Mutation	c.1766G>A
AA Mutation	p.Arg589Gln(p.R589Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42287945:42287945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901T>C
AA Mutation	p.Ser301Pro(p.S301P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000575354
Start	42289329:42289329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532264982
CDS Mutation	c.1283G>A
AA Mutation	p.Arg428His(p.R428H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000575354
Start	42289903:42289903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201788031
CDS Mutation	c.1416C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000575354
Start	42294978:42294978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144544276
CDS Mutation	c.4614G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000575354
Start	42287965:42287965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.921T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000575354
Start	42288988:42288988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1032T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000575354
Start	42287667:42287667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000575354
Start	42293038:42293038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768033538
CDS Mutation	c.3552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000575354
Start	42290317:42290317(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1553delC
AA Mutation	p.Pro518ArgfsTer5(p.P518Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000575354
Start	42291117:42291117(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs34000070
CDS Mutation	c.2353delG
AA Mutation	p.Ala785ProfsTer139(p.A785Pfs*139)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000575354
Start	42293224:42293224(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3743delC
AA Mutation	p.Pro1248HisfsTer54(p.P1248Hfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000575354
Start	42294946:42294946(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4586delC
AA Mutation	p.Pro1529LeufsTer91(p.P1529Lfs*91)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000575354
Start	42290289:42290289(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1526delC
AA Mutation	p.Pro509HisfsTer14(p.P509Hfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000575354
Start	42293096:42293096(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3613delC
AA Mutation	p.Arg1205GlyfsTer97(p.R1205Gfs*97)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000575354
Start	42291091:42291091(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2327delC
AA Mutation	p.Pro776LeufsTer148(p.P776Lfs*148)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000575354
Start	42293126:42293126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3640C>T
AA Mutation	p.Arg1214Ter(p.R1214*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000575354
Start	42290638:42290638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1870G>T
AA Mutation	p.Gly624Ter(p.G624*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000575354
Start	42290653:42290653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1885C>T
AA Mutation	p.Gln629Ter(p.Q629*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000575354
Start	42293654:42293655(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3862dupG
AA Mutation	p.Glu1288GlyfsTer56(p.E1288Gfs*56)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000575354
Start	42293133:42293134(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3649dupA
AA Mutation	p.Thr1217AsnfsTer6(p.T1217Nfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000575354
Start	42291557:42291557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2699-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CIC

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000575354
Start	42289055:42289055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099G>T
AA Mutation	p.Glu367Ter(p.E367*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript