Colon Cancer: Gene >> TSHZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75286281:75286281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.874C>T
AA Mutation	p.Arg292Cys(p.R292C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75286282:75286282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.875G>A
AA Mutation	p.Arg292His(p.R292H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75288184:75288184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2777G>T
AA Mutation	p.Arg926Met(p.R926M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75288085:75288085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2678A>G
AA Mutation	p.Asn893Ser(p.N893S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75286004:75286004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.597G>C
AA Mutation	p.Trp199Cys(p.W199C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75286005:75286005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598C>A
AA Mutation	p.His200Asn(p.H200N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75287089:75287089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199773721
CDS Mutation	c.1682C>T
AA Mutation	p.Thr561Met(p.T561M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75287712:75287712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2305G>A
AA Mutation	p.Asp769Asn(p.D769N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75286222:75286222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815G>T
AA Mutation	p.Arg272Leu(p.R272L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75288132:75288132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560496526
CDS Mutation	c.2725C>T
AA Mutation	p.Arg909Trp(p.R909W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75288451:75288451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535727349
CDS Mutation	c.3044C>T
AA Mutation	p.Ser1015Leu(p.S1015L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75286846:75286846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1439C>T
AA Mutation	p.Ala480Val(p.A480V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75287731:75287731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2324A>G
AA Mutation	p.Tyr775Cys(p.Y775C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75286522:75286522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749830078
CDS Mutation	c.1115C>T
AA Mutation	p.Ala372Val(p.A372V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580243
Start	75287903:75287903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2496G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580243
Start	75288278:75288278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377168829
CDS Mutation	c.2871G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580243
Start	75286748:75286748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202060462
CDS Mutation	c.1341G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580243
Start	75287525:75287525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2118A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580243
Start	75287963:75287963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190970728
CDS Mutation	c.2556G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580243
Start	75285629:75285629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143847918
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580243
Start	75288389:75288389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2982C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580243
Start	75288002:75288002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748243048
CDS Mutation	c.2595C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580243
Start	75287498:75287498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529413067
CDS Mutation	c.2091C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000580243
Start	75286488:75286488(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1086delC
AA Mutation	p.Cys363AlafsTer14(p.C363Afs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000580243
Start	75288485:75288485(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3082delG
AA Mutation	p.Ala1028ProfsTer41(p.A1028Pfs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000580243
Start	75286152:75286153(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.746_747delAA
AA Mutation	p.Lys249ArgfsTer24(p.K249Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000580243
Start	75286754:75286755(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1347_1348delTA
AA Mutation	p.Lys450GlufsTer47(p.K450Efs*47)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TSHZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75288451:75288451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535727349
CDS Mutation	c.3044C>T
AA Mutation	p.Ser1015Leu(p.S1015L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75287887:75287887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2480C>T
AA Mutation	p.Ser827Leu(p.S827L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75287061:75287061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1654C>A
AA Mutation	p.Leu552Ile(p.L552I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000580243
Start	75288313:75288313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2906T>C
AA Mutation	p.Val969Ala(p.V969A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580243
Start	75286040:75286040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138154252
CDS Mutation	c.633G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000580243
Start	75286928:75286928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779857751
CDS Mutation	c.1521G>A
Mutation Classification	Silent
Feature Type	Transcript