Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TPP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102637189:102637189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1786A>C
AA Mutation	p.Asn596His(p.N596H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102657138:102657138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3035A>C
AA Mutation	p.Glu1012Ala(p.E1012A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102657101:102657101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2998A>G
AA Mutation	p.Thr1000Ala(p.T1000A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102643237:102643237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2036C>T
AA Mutation	p.Ser679Leu(p.S679L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102643319:102643319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2118C>A
AA Mutation	p.Phe706Leu(p.F706L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102657166:102657166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3063T>G
AA Mutation	p.Phe1021Leu(p.F1021L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102604820:102604820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560814385
CDS Mutation	c.193G>A
AA Mutation	p.Val65Ile(p.V65I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102674311:102674311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375137754
CDS Mutation	c.3361G>A
AA Mutation	p.Val1121Ile(p.V1121I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102648983:102648983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2705G>A
AA Mutation	p.Arg902His(p.R902H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102657131:102657131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3028G>T
AA Mutation	p.Asp1010Tyr(p.D1010Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102630179:102630179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1228T>C
AA Mutation	p.Ser410Pro(p.S410P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102627905:102627905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.997A>G
AA Mutation	p.Thr333Ala(p.T333A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102616427:102616427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422T>C
AA Mutation	p.Val141Ala(p.V141A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102616402:102616402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397C>T
AA Mutation	p.Arg133Trp(p.R133W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376065
Start	102636358:102636358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377541134
CDS Mutation	c.1644C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376065
Start	102644956:102644956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2340A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376065
Start	102678250:102678250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3684C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376065
Start	102604819:102604819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376421521
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376065
Start	102647326:102647326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150615380
CDS Mutation	c.2610C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376065
Start	102636247:102636247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748887989
CDS Mutation	c.1533C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376065
Start	102614148:102614148(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.347delA
AA Mutation	p.Asn116MetfsTer54(p.N116Mfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376065
Start	102640342:102640342(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1989delT
AA Mutation	p.Phe663LeufsTer13(p.F663Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000376065
Start	102637133:102637133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1730C>A
AA Mutation	p.Ser577Ter(p.S577*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000376065
Start	102648943:102648943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2665C>T
AA Mutation	p.Arg889Ter(p.R889*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376065
Start	102604812:102604813(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.190dupA
AA Mutation	p.Ile64AsnfsTer3(p.I64Nfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376065
Start	102643366:102643367(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2165_2166insAAACTTA
AA Mutation	p.Phe722LeufsTer12(p.F722Lfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000376065
Start	102645010:102645010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2393+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TPP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102616489:102616489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202026163
CDS Mutation	c.484G>A
AA Mutation	p.Gly162Ser(p.G162S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376065
Start	102664880:102664880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3287T>G
AA Mutation	p.Ile1096Ser(p.I1096S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376065
Start	102618835:102618835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781303333
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376065
Start	102627895:102627895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776689512
CDS Mutation	c.987C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000376065
Start	102640334:102640334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1978C>T
AA Mutation	p.Arg660Ter(p.R660*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000376065
Start	102636261:102636261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1547C>A
AA Mutation	p.Ser516Ter(p.S516*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript