Colon Cancer: Gene >> TLE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262953
Start	3005451:3005451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1882G>A
AA Mutation	p.Asp628Asn(p.D628N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262953
Start	3011087:3011087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947G>A
AA Mutation	p.Gly316Glu(p.G316E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262953
Start	3005469:3005469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764714978
CDS Mutation	c.1864C>T
AA Mutation	p.Arg622Cys(p.R622C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262953
Start	3002496:3002496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1904C>T
AA Mutation	p.Ser635Phe(p.S635F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262953
Start	3015696:3015696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635G>A
AA Mutation	p.Gly212Asp(p.G212D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262953
Start	3006460:3006460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1460A>G
AA Mutation	p.Gln487Arg(p.Q487R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262953
Start	3011033:3011033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752674140
CDS Mutation	c.1001C>T
AA Mutation	p.Thr334Met(p.T334M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262953
Start	3005815:3005815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1654G>A
AA Mutation	p.Ala552Thr(p.A552T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262953
Start	3028711:3028711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262953
Start	3027856:3027856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774732505
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262953
Start	3006468:3006468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1452C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262953
Start	3005846:3005846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112201116
CDS Mutation	c.1623C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262953
Start	3009580:3009580(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1135delC
AA Mutation	p.Gln379ArgfsTer13(p.Q379Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262953
Start	3013798:3013798(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.744delC
AA Mutation	p.Ser249AlafsTer43(p.S249Afs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262953
Start	3009688:3009688(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1027delC
AA Mutation	p.Leu343Ter(p.L343*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262953
Start	3005509:3005510(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs763658500
CDS Mutation	c.1823dupG
AA Mutation	p.Leu609ProfsTer20(p.L609Pfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262953
Start	3005856:3005857(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs756800910
CDS Mutation	c.1612dupC
AA Mutation	p.Arg538ProfsTer59(p.R538Pfs*59)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TLE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262953
Start	3005797:3005797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774062563
CDS Mutation	c.1672G>A
AA Mutation	p.Asp558Asn(p.D558N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262953
Start	3014605:3014605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688G>A
AA Mutation	p.Glu230Lys(p.E230K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262953
Start	3017850:3017850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.560C>T
AA Mutation	p.Ala187Val(p.A187V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript