Colon Cancer: Gene >> SUCO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172585080:172585080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1561A>G
AA Mutation	p.Thr521Ala(p.T521A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172557695:172557695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.633G>T
AA Mutation	p.Lys211Asn(p.K211N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263688
Start	172570664:172570664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983G>A
AA Mutation	p.Ser328Asn(p.S328N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172589041:172589041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752014324
CDS Mutation	c.1940G>A
AA Mutation	p.Arg647His(p.R647H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172533484:172533484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.49T>C
AA Mutation	p.Cys17Arg(p.C17R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172555902:172555902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116122588
CDS Mutation	c.322G>A
AA Mutation	p.Val108Met(p.V108M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172589009:172589009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1908G>C
AA Mutation	p.Trp636Cys(p.W636C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172589047:172589047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199510939
CDS Mutation	c.1946G>A
AA Mutation	p.Arg649Gln(p.R649Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172610105:172610105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772243543
CDS Mutation	c.3611G>A
AA Mutation	p.Arg1204Gln(p.R1204Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172590989:172590989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2831G>A
AA Mutation	p.Arg944Gln(p.R944Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172610165:172610165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3671C>T
AA Mutation	p.Ser1224Leu(p.S1224L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172585069:172585069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1550C>A
AA Mutation	p.Thr517Asn(p.T517N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172585071:172585071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1552G>C
AA Mutation	p.Glu518Gln(p.E518Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172589323:172589323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2222T>C
AA Mutation	p.Ile741Thr(p.I741T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263688
Start	172551590:172551590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376930360
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263688
Start	172609920:172609920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756766487
CDS Mutation	c.3426G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263688
Start	172575572:172575572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1212G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000263688
Start	172610110:172610110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3616C>T
AA Mutation	p.Arg1206Ter(p.R1206*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000263688
Start	172553332:172553332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250G>T
AA Mutation	p.Glu84Ter(p.E84*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000263688
Start	172573901:172573901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1060G>T
AA Mutation	p.Glu354Ter(p.E354*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263688
Start	172557686:172557687(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.627dupA
AA Mutation	p.Gly210ArgfsTer9(p.G210Rfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SUCO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172590989:172590989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2831G>A
AA Mutation	p.Arg944Gln(p.R944Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172610150:172610150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3656T>C
AA Mutation	p.Leu1219Pro(p.L1219P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172575532:172575532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172A>C
AA Mutation	p.Lys391Thr(p.K391T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172609930:172609930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3436G>T
AA Mutation	p.Asp1146Tyr(p.D1146Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172589496:172589496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2395G>T
AA Mutation	p.Val799Phe(p.V799F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172589757:172589757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746592153
CDS Mutation	c.2656G>T
AA Mutation	p.Asp886Tyr(p.D886Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172591060:172591060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2902G>T
AA Mutation	p.Ala968Ser(p.A968S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172602715:172602715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3193G>T
AA Mutation	p.Asp1065Tyr(p.D1065Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172569114:172569114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828G>T
AA Mutation	p.Lys276Asn(p.K276N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263688
Start	172589047:172589047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199510939
CDS Mutation	c.1946G>A
AA Mutation	p.Arg649Gln(p.R649Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263688
Start	172588937:172588937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1836G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263688
Start	172609920:172609920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756766487
CDS Mutation	c.3426G>A
Mutation Classification	Silent
Feature Type	Transcript