Colon Cancer: Gene >> CGN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151534085:151534085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2853G>T
AA Mutation	p.Glu951Asp(p.E951D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151523519:151523519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1226T>C
AA Mutation	p.Leu409Pro(p.L409P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151532559:151532559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115631509
CDS Mutation	c.2729G>A
AA Mutation	p.Arg910Gln(p.R910Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151518700:151518700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.181G>A
AA Mutation	p.Ala61Thr(p.A61T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151537263:151537263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3529G>A
AA Mutation	p.Asp1177Asn(p.D1177N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151524827:151524827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765530896
CDS Mutation	c.1555C>T
AA Mutation	p.Arg519Trp(p.R519W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151523477:151523477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1184A>G
AA Mutation	p.Gln395Arg(p.Q395R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151524851:151524851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579G>C
AA Mutation	p.Glu527Gln(p.E527Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151527064:151527064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753255750
CDS Mutation	c.1853G>A
AA Mutation	p.Arg618Gln(p.R618Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151518832:151518832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.313T>C
AA Mutation	p.Tyr105His(p.Y105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151524243:151524243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761721175
CDS Mutation	c.1286G>A
AA Mutation	p.Arg429His(p.R429H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151519205:151519205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686G>A
AA Mutation	p.Arg229His(p.R229H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151530107:151530107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2305C>T
AA Mutation	p.Arg769Trp(p.R769W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271636
Start	151534106:151534106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371262483
CDS Mutation	c.2874C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271636
Start	151536798:151536798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000271636
Start	151530086:151530086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2284C>T
AA Mutation	p.Arg762Ter(p.R762*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CGN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271636
Start	151533987:151533987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757845776
CDS Mutation	c.2755C>T
AA Mutation	p.Arg919Trp(p.R919W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript