Colon Cancer: Gene >> SLC22A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000200652
Start	132327354:132327354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902C>T
AA Mutation	p.Ala301Val(p.A301V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000200652
Start	132340670:132340670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1550A>C
AA Mutation	p.Glu517Ala(p.E517A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200652
Start	132322200:132322200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200652
Start	132334847:132334847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779825520
CDS Mutation	c.1176G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200652
Start	132322243:132322243(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.717delT
AA Mutation	p.Phe239LeufsTer25(p.F239Lfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200652
Start	132343773:132343773(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1600delA
AA Mutation	p.Thr534GlnfsTer14(p.T534Qfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200652
Start	132312193:132312194(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.430dupC
AA Mutation	p.Leu144ProfsTer136(p.L144Pfs*136)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200652
Start	132335938:132335939(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1387dupG
AA Mutation	p.Val463GlyfsTer33(p.V463Gfs*33)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200652
Start	132322242:132322243(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.717dupT
AA Mutation	p.Ala240CysfsTer40(p.A240Cfs*40)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000200652
Start	132313660:132313662(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.544_546delGGC
AA Mutation	p.Gly182del(p.G182del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC22A4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000200652
Start	132313683:132313683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.567C>A
AA Mutation	p.Phe189Leu(p.F189L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000200652
Start	132335859:132335859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1303T>G
AA Mutation	p.Phe435Val(p.F435V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000200652
Start	132335817:132335817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1262-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript