Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TRPA1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262209
Start	72069196:72069196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.271C>A
AA Mutation	p.Leu91Met(p.L91M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72033706:72033706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2806C>A
AA Mutation	p.Leu936Met(p.L936M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72046605:72046605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760171486
CDS Mutation	c.1969G>A
AA Mutation	p.Glu657Lys(p.E657K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72047186:72047186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1927T>G
AA Mutation	p.Leu643Val(p.L643V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72055822:72055822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1228G>A
AA Mutation	p.Asp410Asn(p.D410N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72036333:72036333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2510T>G
AA Mutation	p.Ile837Ser(p.I837S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72056972:72056972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1139A>G
AA Mutation	p.His380Arg(p.H380R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72036453:72036453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2390G>T
AA Mutation	p.Arg797Met(p.R797M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72075311:72075311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99G>T
AA Mutation	p.Lys33Asn(p.K33N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72075342:72075342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.68A>G
AA Mutation	p.Glu23Gly(p.E23G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72069159:72069159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308A>G
AA Mutation	p.His103Arg(p.H103R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72075381:72075381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.29G>A
AA Mutation	p.Arg10His(p.R10H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72071849:72071849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130G>A
AA Mutation	p.Ala44Thr(p.A44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72023029:72023029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3237G>T
AA Mutation	p.Glu1079Asp(p.E1079D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72056955:72056955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755719558
CDS Mutation	c.1156C>A
AA Mutation	p.Pro386Thr(p.P386T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72069144:72069144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323A>G
AA Mutation	p.Lys108Arg(p.K108R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72023009:72023009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3257C>A
AA Mutation	p.Ser1086Tyr(p.S1086Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72061691:72061691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141174965
CDS Mutation	c.878C>T
AA Mutation	p.Ser293Leu(p.S293L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72038954:72038954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2206C>T
AA Mutation	p.Leu736Phe(p.L736F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72046529:72046529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201119954
CDS Mutation	c.2045C>T
AA Mutation	p.Pro682Leu(p.P682L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72069126:72069126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341T>C
AA Mutation	p.Val114Ala(p.V114A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72063523:72063523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.601C>A
AA Mutation	p.Pro201Thr(p.P201T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72034367:72034367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2566T>G
AA Mutation	p.Cys856Gly(p.C856G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262209
Start	72062802:72062802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262209
Start	72071817:72071817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.162G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262209
Start	72052754:72052754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1656T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262209
Start	72053756:72053756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752559794
CDS Mutation	c.1641C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262209
Start	72038052:72038052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2316T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262209
Start	72052616:72052616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772012081
CDS Mutation	c.1794G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262209
Start	72059399:72059402(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.981_984delTTTA
AA Mutation	p.Tyr327Ter(p.Y327*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262209
Start	72046557:72046557(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs771445400
CDS Mutation	c.2017delA
AA Mutation	p.Thr673HisfsTer23(p.T673Hfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000262209
Start	72069148:72069148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319G>T
AA Mutation	p.Glu107Ter(p.E107*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262209
Start	72055452:72055453(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs770577826
CDS Mutation	c.1512dupA
AA Mutation	p.Gly505ArgfsTer7(p.G505Rfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262209
Start	72023894:72023895(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3068dupT
AA Mutation	p.Leu1023PhefsTer15(p.L1023Ffs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262209
Start	72056981:72056982(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1129_1130insTAATAAACAAAATTAGTTT
AA Mutation	p.Asn377IlefsTer25(p.N377Ifs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000262209
Start	72055685:72055685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1364+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TRPA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72055492:72055492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1473G>T
AA Mutation	p.Lys491Asn(p.K491N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72055722:72055722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1328G>T
AA Mutation	p.Ser443Ile(p.S443I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72057755:72057755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1055C>A
AA Mutation	p.Ser352Tyr(p.S352Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262209
Start	72071817:72071817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767958267
CDS Mutation	c.162G>T
AA Mutation	p.Lys54Asn(p.K54N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262209
Start	72055769:72055769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1281T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262209
Start	72053756:72053756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752559794
CDS Mutation	c.1641C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000262209
Start	72069148:72069148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319G>T
AA Mutation	p.Glu107Ter(p.E107*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000262209
Start	72046511:72046511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2061+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript