Colon Cancer: Gene >> SLC16A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329783
Start	75098077:75098077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150984642
CDS Mutation	c.239G>A
AA Mutation	p.Arg80Gln(p.R80Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329783
Start	75105978:75105978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1463C>T
AA Mutation	p.Pro488Leu(p.P488L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329783
Start	75093774:75093774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.138G>T
AA Mutation	p.Gln46His(p.Q46H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329783
Start	75100680:75100680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329783
Start	75100674:75100674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539147742
CDS Mutation	c.1011G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329783
Start	75105919:75105919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1404T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329783
Start	75100273:75100273(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.614delC
AA Mutation	p.Pro205ArgfsTer41(p.P205Rfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000329783
Start	75100267:75100267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604G>T
AA Mutation	p.Glu202Ter(p.E202*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC16A5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329783
Start	75098101:75098101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263T>G
AA Mutation	p.Val88Gly(p.V88G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329783
Start	75100185:75100185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.522C>A
Mutation Classification	Silent
Feature Type	Transcript