Colon Cancer: Gene >> SLC7A8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316902
Start	23166376:23166376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.316G>A
AA Mutation	p.Asp106Asn(p.D106N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316902
Start	23127245:23127245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1540C>G
AA Mutation	p.Gln514Glu(p.Q514E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316902
Start	23140565:23140565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145886415
CDS Mutation	c.694G>A
AA Mutation	p.Gly232Ser(p.G232S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316902
Start	23129660:23129660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763323196
CDS Mutation	c.1253G>A
AA Mutation	p.Arg418His(p.R418H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316902
Start	23143172:23143172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540015976
CDS Mutation	c.541C>T
AA Mutation	p.Arg181Trp(p.R181W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316902
Start	23128152:23128152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316902
Start	23165346:23165346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781585326
CDS Mutation	c.447G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000316902
Start	23127242:23127242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1543C>T
AA Mutation	p.Gln515Ter(p.Q515*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC7A8

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000316902
Start	23166346:23166346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.346G>T
AA Mutation	p.Gly116Ter(p.G116*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript