Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TEP1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20395569:20395569(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1809G>T
AA Mutation p.Lys603Asn(p.K603N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20380284:20380284(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4954C>T
AA Mutation p.His1652Tyr(p.H1652Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20386568:20386568(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs548257852
CDS Mutation c.2740C>T
AA Mutation p.Arg914Trp(p.R914W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20381616:20381616(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4495G>A
AA Mutation p.Ala1499Thr(p.A1499T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000262715
Start 20405584:20405584(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.737T>C
AA Mutation p.Met246Thr(p.M246T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20405536:20405536(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148090256
CDS Mutation c.785T>C
AA Mutation p.Met262Thr(p.M262T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20371564:20371564(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7145G>A
AA Mutation p.Gly2382Asp(p.G2382D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20390999:20390999(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2195C>A
AA Mutation p.Ala732Glu(p.A732E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20377653:20377653(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5822G>A
AA Mutation p.Arg1941Gln(p.R1941Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20403740:20403740(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147598692
CDS Mutation c.1177C>T
AA Mutation p.Arg393Trp(p.R393W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20384132:20384132(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779605418
CDS Mutation c.3440G>A
AA Mutation p.Arg1147His(p.R1147H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20403730:20403730(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1187G>A
AA Mutation p.Arg396His(p.R396H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20396706:20396706(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1574C>A
AA Mutation p.Ala525Asp(p.A525D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20378990:20378990(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774436082
CDS Mutation c.5243A>G
AA Mutation p.His1748Arg(p.H1748R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20396676:20396676(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769367433
CDS Mutation c.1604G>A
AA Mutation p.Arg535Gln(p.R535Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20408112:20408112(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777621271
CDS Mutation c.328C>T
AA Mutation p.Arg110Trp(p.R110W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20381585:20381585(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4526G>A
AA Mutation p.Gly1509Glu(p.G1509E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20388043:20388043(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2546C>T
AA Mutation p.Ala849Val(p.A849V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20408103:20408103(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.337G>A
AA Mutation p.Ala113Thr(p.A113T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000262715
Start 20378222:20378222(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762759586
CDS Mutation c.5523C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000262715
Start 20403798:20403798(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202055706
CDS Mutation c.1119C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000262715
Start 20379996:20379996(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5061T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000262715
Start 20386491:20386491(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2817C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000262715
Start 20382677:20382677(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752974270
CDS Mutation c.4086G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000262715
Start 20372750:20372750(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771264352
CDS Mutation c.7059G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence frameshift_variant
Transcription ID ENST00000262715
Start 20387928:20387928(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2661delC
AA Mutation p.Leu888TrpfsTer31(p.L888Wfs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 27
Mutation Consequence frameshift_variant
Transcription ID ENST00000262715
Start 20384488:20384488(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3242delG
AA Mutation p.Gly1081ValfsTer26(p.G1081Vfs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 28
Mutation Consequence frameshift_variant
Transcription ID ENST00000262715
Start 20378179:20378179(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs754702761
CDS Mutation c.5566delG
AA Mutation p.Val1856LeufsTer45(p.V1856Lfs*45)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 29
Mutation Consequence frameshift_variant
Transcription ID ENST00000262715
Start 20403743:20403743(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1174delC
AA Mutation p.Arg392AlafsTer22(p.R392Afs*22)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 30
Mutation Consequence frameshift_variant
Transcription ID ENST00000262715
Start 20380448:20380448(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4790delA
AA Mutation p.Lys1597SerfsTer14(p.K1597Sfs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 31
Mutation Consequence frameshift_variant
Transcription ID ENST00000262715
Start 20384487:20384488(version: GRCh38)
Mutation Type INS
dbSNP_RS rs777244307
CDS Mutation c.3242dupG
AA Mutation p.Val1082CysfsTer47(p.V1082Cfs*47)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 32
Mutation Consequence frameshift_variant
Transcription ID ENST00000262715
Start 20401014:20401015(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1518dupG
AA Mutation p.Asn507GlufsTer11(p.N507Efs*11)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> TEP1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20373786:20373786(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766453939
CDS Mutation c.6496C>T
AA Mutation p.Arg2166Trp(p.R2166W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20395945:20395945(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1664C>T
AA Mutation p.Ser555Leu(p.S555L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20388001:20388001(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755874453
CDS Mutation c.2588T>C
AA Mutation p.Phe863Ser(p.F863S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20408243:20408243(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.197G>A
AA Mutation p.Gly66Glu(p.G66E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20381366:20381366(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4594G>T
AA Mutation p.Gly1532Cys(p.G1532C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000262715
Start 20381625:20381625(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4486C>A
AA Mutation p.Leu1496Met(p.L1496M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000262715
Start 20389246:20389246(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762588377
CDS Mutation c.2517G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000262715
Start 20369487:20369487(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7513delT
AA Mutation p.Trp2505GlyfsTer41(p.W2505Gfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript