Colon Cancer: Gene >> TLE4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79574922:79574922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193C>T
AA Mutation	p.Arg65Trp(p.R65W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79652678:79652678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.476C>G
AA Mutation	p.Ala159Gly(p.A159G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79718807:79718807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746243498
CDS Mutation	c.1426C>T
AA Mutation	p.Arg476Trp(p.R476W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79706829:79706829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.866C>G
AA Mutation	p.Ala289Gly(p.A289G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79720277:79720277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1822A>T
AA Mutation	p.Asn608Tyr(p.N608Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79718856:79718856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1475C>T
AA Mutation	p.Ala492Val(p.A492V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000376552
Start	79574873:79574873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144T>G
AA Mutation	p.Ser48Arg(p.S48R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79627389:79627389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331G>A
AA Mutation	p.Val111Met(p.V111M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79652704:79652704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502G>A
AA Mutation	p.Gly168Arg(p.G168R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79708194:79708194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1013A>C
AA Mutation	p.Asn338Thr(p.N338T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79652675:79652675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473C>T
AA Mutation	p.Pro158Leu(p.P158L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79721874:79721874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751862890
CDS Mutation	c.1972G>A
AA Mutation	p.Asp658Asn(p.D658N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79706810:79706810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776714530
CDS Mutation	c.847C>T
AA Mutation	p.Arg283Cys(p.R283C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79718858:79718858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1477G>T
AA Mutation	p.Val493Leu(p.V493L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79718949:79718949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1568C>T
AA Mutation	p.Pro523Leu(p.P523L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79576145:79576145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220T>C
AA Mutation	p.Ser74Pro(p.S74P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79720158:79720158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1703G>A
AA Mutation	p.Arg568His(p.R568H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79709651:79709651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1292G>A
AA Mutation	p.Arg431His(p.R431H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376552
Start	79722460:79722460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1996C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376552
Start	79708735:79708735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200253291
CDS Mutation	c.1212C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376552
Start	79652691:79652691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555373051
CDS Mutation	c.489C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376552
Start	79708132:79708132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.951T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376552
Start	79705933:79705933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.774T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376552
Start	79708672:79708672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373028396
CDS Mutation	c.1149C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376552
Start	79722498:79722498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2034G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000376552
Start	79722565:79722565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2101G>T
AA Mutation	p.Glu701Ter(p.E701*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000376552
Start	79704813:79704813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640C>T
AA Mutation	p.Arg214Ter(p.R214*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376552
Start	79576135:79576136(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.210_211insCTTCA
AA Mutation	p.Tyr71LeufsTer9(p.Y71Lfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376552
Start	79720180:79720181(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1725_1726insATAAAAG
AA Mutation	p.Ser576IlefsTer53(p.S576Ifs*53)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TLE4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79725138:79725138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2316T>G
AA Mutation	p.Ile772Met(p.I772M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79573693:79573693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.50C>A
AA Mutation	p.Pro17Gln(p.P17Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79612661:79612661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258G>T
AA Mutation	p.Glu86Asp(p.E86D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376552
Start	79718914:79718914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1533G>T
AA Mutation	p.Lys511Asn(p.K511N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376552
Start	79721804:79721804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1902C>A
Mutation Classification	Silent
Feature Type	Transcript