Colon Cancer: Gene >> SLC6A7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000230671
Start	150202694:150202694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1078G>A
AA Mutation	p.Ala360Thr(p.A360T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000230671
Start	150202429:150202429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941C>T
AA Mutation	p.Thr314Met(p.T314M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000230671
Start	150204013:150204013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1307T>C
AA Mutation	p.Leu436Pro(p.L436P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230671
Start	150196792:150196792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000230671
Start	150194862:150194862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000230671
Start	150202585:150202586(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.969_970insC
AA Mutation	p.Phe324LeufsTer76(p.F324Lfs*76)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000230671
Start	150194752:150194753(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.63dupC
AA Mutation	p.Ser22GlnfsTer2(p.S22Qfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC6A7

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000230671
Start	150202637:150202638(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1021_1022delAT
AA Mutation	p.Ile341LeufsTer58(p.I341Lfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript