Colon Cancer: Gene >> TMPO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000556029
Start	98544333:98544333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767G>T
AA Mutation	p.Arg256Ile(p.R256I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266732
Start	98533366:98533366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109C>A
AA Mutation	p.Ser370Tyr(p.S370Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266732
Start	98534059:98534059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376075320
CDS Mutation	c.1802C>T
AA Mutation	p.Ala601Val(p.A601V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266732
Start	98533959:98533959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702G>A
AA Mutation	p.Ala568Thr(p.A568T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266732
Start	98533351:98533351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1094G>T
AA Mutation	p.Ser365Ile(p.S365I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266732
Start	98515991:98515991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124C>A
AA Mutation	p.Leu42Met(p.L42M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266732
Start	98533546:98533546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1289C>A
AA Mutation	p.Pro430His(p.P430H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000556029
Start	98547804:98547804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770801240
CDS Mutation	c.1311C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000556029
Start	98547767:98547767(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1280delT
AA Mutation	p.Leu427CysfsTer13(p.L427Cfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266732
Start	98527894:98527894(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs774744805
CDS Mutation	c.295delA
AA Mutation	p.Thr99LeufsTer12(p.T99Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266732
Start	98516047:98516047(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.183delG
AA Mutation	p.Pro63ArgfsTer48(p.P63Rfs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000556029
Start	98544529:98544529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871G>T
AA Mutation	p.Glu291Ter(p.E291*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000266732
Start	98533572:98533572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315G>T
AA Mutation	p.Glu439Ter(p.E439*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000556029
Start	98547707:98547708(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1220dupA
AA Mutation	p.Arg409ThrfsTer36(p.R409Tfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000556029
Start	98547766:98547767(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1280dupT
AA Mutation	p.Leu427PhefsTer18(p.L427Ffs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000266732
Start	98533629:98533631(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1376_1378delCTT
AA Mutation	p.Ser459del(p.S459del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TMPO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266732
Start	98533369:98533369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199943517
CDS Mutation	c.1112C>T
AA Mutation	p.Pro371Leu(p.P371L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266732
Start	98533620:98533620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763388598
CDS Mutation	c.1363G>A
AA Mutation	p.Glu455Lys(p.E455K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266732
Start	98532858:98532858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.601A>G
AA Mutation	p.Arg201Gly(p.R201G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266732
Start	98533963:98533963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1706T>G
AA Mutation	p.Leu569Arg(p.L569R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266732
Start	98532966:98532966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770791830
CDS Mutation	c.709G>A
AA Mutation	p.Glu237Lys(p.E237K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266732
Start	98533797:98533797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1540C>T
AA Mutation	p.Pro514Ser(p.P514S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000266732
Start	98531835:98531835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562G>T
AA Mutation	p.Glu188Ter(p.E188*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000266732
Start	98533680:98533680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1423G>T
AA Mutation	p.Glu475Ter(p.E475*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000556029
Start	98546377:98546377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1009G>T
AA Mutation	p.Glu337Ter(p.E337*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript