Colon Cancer: Gene >> SELL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000236147
Start	169708572:169708572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356C>A
AA Mutation	p.Ser119Tyr(p.S119Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000236147
Start	169708553:169708553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375G>T
AA Mutation	p.Glu125Asp(p.E125D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000236147
Start	169707381:169707381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580A>G
AA Mutation	p.Asn194Asp(p.N194D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000236147
Start	169707397:169707397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.564C>G
AA Mutation	p.Ile188Met(p.I188M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236147
Start	169703418:169703418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.828A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000236147
Start	169710455:169710455(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.105delG
AA Mutation	p.Trp36GlyfsTer26(p.W36Gfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000236147
Start	169701641:169701641(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1039delC
AA Mutation	p.Leu347SerfsTer25(p.L347Sfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000236147
Start	169708750:169708751(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.177dupA
AA Mutation	p.Pro60ThrfsTer8(p.P60Tfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000236147
Start	169707395:169707396(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.565_566insTAAGCT
AA Mutation	p.Asn189delinsIleSerTyr(p.N189delinsISY)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SELL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000236147
Start	169703306:169703306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.940A>G
AA Mutation	p.Thr314Ala(p.T314A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000236147
Start	169708523:169708523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405G>T
AA Mutation	p.Lys135Asn(p.K135N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000236147
Start	169703391:169703391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.855T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000236147
Start	169701641:169701641(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1039delC
AA Mutation	p.Leu347SerfsTer25(p.L347Sfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000236147
Start	169704622:169704622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751G>T
AA Mutation	p.Glu251Ter(p.E251*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript