Colon Cancer: Gene >> TLR9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223900:52223900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416C>A
AA Mutation	p.Pro139His(p.P139H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223669:52223669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749495421
CDS Mutation	c.647G>A
AA Mutation	p.Arg216His(p.R216H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52221641:52221641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2675G>A
AA Mutation	p.Arg892Gln(p.R892Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223307:52223307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202131815
CDS Mutation	c.1009C>T
AA Mutation	p.Arg337Cys(p.R337C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52222040:52222040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2276C>T
AA Mutation	p.Ala759Val(p.A759V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52222644:52222644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756045938
CDS Mutation	c.1672C>T
AA Mutation	p.Pro558Ser(p.P558S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52222626:52222626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200059070
CDS Mutation	c.1690G>A
AA Mutation	p.Val564Met(p.V564M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52221602:52221602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376675219
CDS Mutation	c.2714G>A
AA Mutation	p.Arg905His(p.R905H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223744:52223744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572C>T
AA Mutation	p.Ala191Val(p.A191V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223535:52223535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781G>A
AA Mutation	p.Ala261Thr(p.A261T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52224302:52224302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199759037
CDS Mutation	c.14G>A
AA Mutation	p.Arg5His(p.R5H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223462:52223462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854G>A
AA Mutation	p.Arg285His(p.R285H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223198:52223198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118G>A
AA Mutation	p.Gly373Asp(p.G373D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52221956:52221956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2360G>A
AA Mutation	p.Arg787Gln(p.R787Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52221584:52221584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2732G>A
AA Mutation	p.Arg911His(p.R911H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223546:52223546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.770G>A
AA Mutation	p.Arg257His(p.R257H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52221649:52221649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149908506
CDS Mutation	c.2667C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52221937:52221937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55919832
CDS Mutation	c.2379G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52221820:52221820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2496G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52223965:52223965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52223560:52223560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200139837
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000360658
Start	52222162:52222162(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2154delC
AA Mutation	p.Gly719AlafsTer37(p.G719Afs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TLR9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52221740:52221740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763585272
CDS Mutation	c.2576G>A
AA Mutation	p.Arg859Gln(p.R859Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223159:52223159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1157C>A
AA Mutation	p.Pro386Gln(p.P386Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223576:52223576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749742285
CDS Mutation	c.740G>A
AA Mutation	p.Arg247His(p.R247H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52223432:52223432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.884C>A
AA Mutation	p.Ser295Tyr(p.S295Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52221642:52221642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2674C>T
AA Mutation	p.Arg892Trp(p.R892W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360658
Start	52222370:52222370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202082899
CDS Mutation	c.1946G>A
AA Mutation	p.Arg649His(p.R649H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360658
Start	52223146:52223146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1170G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000360658
Start	52221729:52221729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2587C>T
AA Mutation	p.Arg863Ter(p.R863*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript