Colon Cancer: Gene >> SULT1B1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000310613
Start	69730501:69730501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778G>T
AA Mutation	p.Gly260Trp(p.G260W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310613
Start	69734157:69734157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483G>T
AA Mutation	p.Glu161Asp(p.E161D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310613
Start	69749786:69749786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779362138
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Trp(p.R104W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310613
Start	69733435:69733435(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.575delT
AA Mutation	p.Leu192CysfsTer6(p.L192Cfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310613
Start	69755127:69755127(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.91delA
AA Mutation	p.Ile31LeufsTer12(p.I31Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000310613
Start	69727175:69727176(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.803_804insAAAG
AA Mutation	p.Tyr268Ter(p.Y268*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310613
Start	69755206:69755207(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.11dupC
AA Mutation	p.Asp6ArgfsTer27(p.D6Rfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000310613
Start	69727174:69727175(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.804_805insATATTA
AA Mutation	p.Tyr268_Phe269insIleLeu(p.Y268_F269insIL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SULT1B1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310613
Start	69727152:69727152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.827A>G
AA Mutation	p.Lys276Arg(p.K276R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310613
Start	69730654:69730654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.625A>C
AA Mutation	p.Ile209Leu(p.I209L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript