Colon Cancer: Gene >> RNGTT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369485
Start	88929029:88929029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759501463
CDS Mutation	c.323G>A
AA Mutation	p.Arg108His(p.R108H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369485
Start	88614373:88614373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1529A>T
AA Mutation	p.Tyr510Phe(p.Y510F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369485
Start	88614277:88614277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1625C>T
AA Mutation	p.Ala542Val(p.A542V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369485
Start	88929210:88929210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232G>T
AA Mutation	p.Asp78Tyr(p.D78Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369485
Start	88844446:88844446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1180G>A
AA Mutation	p.Glu394Lys(p.E394K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369485
Start	88890575:88890575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.816G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369485
Start	88614327:88614327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1575C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000369485
Start	88614317:88614317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1585C>T
AA Mutation	p.Gln529Ter(p.Q529*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RNGTT

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369485
Start	88941161:88941161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84G>A
Mutation Classification	Silent
Feature Type	Transcript