Colon Cancer: Gene >> TLE6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246112
Start	2993556:2993556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1511T>A
AA Mutation	p.Ile504Asn(p.I504N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246112
Start	2987752:2987752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587G>A
AA Mutation	p.Cys196Tyr(p.C196Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246112
Start	2987787:2987787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622T>G
AA Mutation	p.Ser208Ala(p.S208A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246112
Start	2981558:2981558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527349785
CDS Mutation	c.155C>T
AA Mutation	p.Ala52Val(p.A52V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000246112
Start	2989553:2989553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760297974
CDS Mutation	c.1012C>T
AA Mutation	p.Arg338Cys(p.R338C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000246112
Start	2978283:2978283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50C>T
AA Mutation	p.Ser17Leu(p.S17L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000246112
Start	2993572:2993572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1527C>G
AA Mutation	p.Phe509Leu(p.F509L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000246112
Start	2994060:2994060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201913892
CDS Mutation	c.1579G>A
AA Mutation	p.Val527Ile(p.V527I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000246112
Start	2987167:2987167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.470A>T
AA Mutation	p.Asp157Val(p.D157V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246112
Start	2994092:2994092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1611C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246112
Start	2989142:2989142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569545270
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246112
Start	2987123:2987123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757907159
CDS Mutation	c.426G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246112
Start	2991867:2991867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1269A>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TLE6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246112
Start	2980149:2980149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.101A>G
AA Mutation	p.Gln34Arg(p.Q34R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246112
Start	2978268:2978268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.35C>A
AA Mutation	p.Pro12His(p.P12H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246112
Start	2994092:2994092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1611C>A
AA Mutation	p.Phe537Leu(p.F537L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246112
Start	2987917:2987917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645C>A
Mutation Classification	Silent
Feature Type	Transcript