Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LCT

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135788385:135788385(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs577825311
CDS Mutation c.5723G>A
AA Mutation p.Arg1908His(p.R1908H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135789732:135789732(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5402C>T
AA Mutation p.Ala1801Val(p.A1801V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135788472:135788472(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5636A>C
AA Mutation p.Glu1879Ala(p.E1879A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135809152:135809152(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3195G>T
AA Mutation p.Glu1065Asp(p.E1065D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135812617:135812617(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2047C>A
AA Mutation p.Leu683Met(p.L683M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135812472:135812472(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2192G>A
AA Mutation p.Gly731Glu(p.G731E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135817348:135817348(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1700C>A
AA Mutation p.Ser567Tyr(p.S567Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135817540:135817540(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1508C>T
AA Mutation p.Ala503Val(p.A503V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135809294:135809294(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3053T>C
AA Mutation p.Leu1018Ser(p.L1018S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135836698:135836698(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.472G>A
AA Mutation p.Ala158Thr(p.A158T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135808612:135808612(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3735G>T
AA Mutation p.Met1245Ile(p.M1245I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135800723:135800723(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4750G>T
AA Mutation p.Asp1584Tyr(p.D1584Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135812737:135812737(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1927G>A
AA Mutation p.Ala643Thr(p.A643T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135798083:135798083(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs557029000
CDS Mutation c.4922T>C
AA Mutation p.Val1641Ala(p.V1641A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135808589:135808589(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772613553
CDS Mutation c.3758C>T
AA Mutation p.Thr1253Met(p.T1253M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135812875:135812875(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1789G>A
AA Mutation p.Val597Met(p.V597M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135836970:135836970(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.200C>A
AA Mutation p.Pro67Gln(p.P67Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135804888:135804888(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4343G>A
AA Mutation p.Arg1448His(p.R1448H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135807369:135807369(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs185632404
CDS Mutation c.3932G>A
AA Mutation p.Arg1311Gln(p.R1311Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135808599:135808599(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3748C>A
AA Mutation p.Pro1250Thr(p.P1250T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135833175:135833175(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.656T>C
AA Mutation p.Val219Ala(p.V219A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135804053:135804053(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752406025
CDS Mutation c.4540C>T
AA Mutation p.Arg1514Trp(p.R1514W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135808631:135808631(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768506428
CDS Mutation c.3716C>T
AA Mutation p.Ser1239Leu(p.S1239L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135808657:135808657(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3690G>T
AA Mutation p.Gln1230His(p.Q1230H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135812893:135812893(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1771C>T
AA Mutation p.Pro591Ser(p.P591S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135790746:135790746(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5247G>T
AA Mutation p.Glu1749Asp(p.E1749D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135798074:135798074(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4931C>T
AA Mutation p.Thr1644Met(p.T1644M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135833125:135833125(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.706T>G
AA Mutation p.Ser236Ala(p.S236A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135817808:135817808(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs192524573
CDS Mutation c.1240C>T
AA Mutation p.Arg414Cys(p.R414C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135803949:135803949(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4644C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135790818:135790818(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs569770794
CDS Mutation c.5175G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135809923:135809923(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs547442018
CDS Mutation c.2424T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135817782:135817782(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1266C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135836717:135836717(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747518550
CDS Mutation c.453C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135805007:135805007(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199901583
CDS Mutation c.4224G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135789752:135789752(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5382G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135803946:135803946(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778443461
CDS Mutation c.4647C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135809932:135809932(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772265393
CDS Mutation c.2415C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135808531:135808531(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375845174
CDS Mutation c.3816C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135809647:135809647(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761282404
CDS Mutation c.2700C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135836549:135836549(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369174474
CDS Mutation c.621C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135809926:135809926(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2421C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135829626:135829626(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.771G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135817890:135817890(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1158C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135822058:135822058(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.948T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135817860:135817860(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753445014
CDS Mutation c.1188C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135809617:135809617(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752135039
CDS Mutation c.2730C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence frameshift_variant
Transcription ID ENST00000264162
Start 135809105:135809105(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3242delC
AA Mutation p.Pro1081GlnfsTer3(p.P1081Qfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 49
Mutation Consequence frameshift_variant
Transcription ID ENST00000264162
Start 135809566:135809566(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2781delA
AA Mutation p.Gly928AlafsTer16(p.G928Afs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 50
Mutation Consequence frameshift_variant
Transcription ID ENST00000264162
Start 135808805:135808806(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3541_3542insCC
AA Mutation p.Leu1181SerfsTer2(p.L1181Sfs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 51
Mutation Consequence protein_altering_variant
Transcription ID ENST00000264162
Start 135812669:135812670(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1994_1995insCACATG
AA Mutation p.Glu665delinsAspThrTrp(p.E665delinsDTW)
Mutation Classification In_Frame_Ins
Feature Type Transcript

Rectum Cancer: Gene >> LCT

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135809463:135809463(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774955926
CDS Mutation c.2884G>A
AA Mutation p.Asp962Asn(p.D962N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135817715:135817715(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1333G>A
AA Mutation p.Gly445Ser(p.G445S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135809781:135809781(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2566C>A
AA Mutation p.Leu856Ile(p.L856I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135788361:135788361(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5747G>A
AA Mutation p.Arg1916Gln(p.R1916Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264162
Start 135808712:135808712(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3635G>T
AA Mutation p.Arg1212Ile(p.R1212I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135809932:135809932(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772265393
CDS Mutation c.2415C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135812330:135812330(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2334T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000264162
Start 135836699:135836699(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201744785
CDS Mutation c.471C>T
Mutation Classification Silent
Feature Type Transcript