Colon Cancer: Gene >> SLC14A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321925
Start	45736533:45736533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367901541
CDS Mutation	c.548C>T
AA Mutation	p.Ala183Val(p.A183V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321925
Start	45749837:45749837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1056G>A
AA Mutation	p.Met352Ile(p.M352I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321925
Start	45749802:45749802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1021C>T
AA Mutation	p.Pro341Ser(p.P341S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321925
Start	45731116:45731116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253C>G
AA Mutation	p.Leu85Val(p.L85V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321925
Start	45739173:45739173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.674C>A
AA Mutation	p.Ser225Tyr(p.S225Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000321925
Start	45749849:45749849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1068T>A
AA Mutation	p.Asn356Lys(p.N356K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000321925
Start	45736508:45736508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138222201
CDS Mutation	c.523G>A
AA Mutation	p.Val175Ile(p.V175I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000321925
Start	45730436:45730436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.116C>T
AA Mutation	p.Thr39Ile(p.T39I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC14A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321925
Start	45749929:45749929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1148G>T
AA Mutation	p.Arg383Ile(p.R383I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321925
Start	45734342:45734342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.410C>T
AA Mutation	p.Ser137Leu(p.S137L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000321925
Start	45739308:45739308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777313922
CDS Mutation	c.809C>T
AA Mutation	p.Ala270Val(p.A270V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript