Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TIAM1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31225883:31225883(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1652C>T
AA Mutation p.Ala551Val(p.A551V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31217663:31217663(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2032C>T
AA Mutation p.Arg678Cys(p.R678C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31154260:31154260(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777057988
CDS Mutation c.3158G>A
AA Mutation p.Arg1053His(p.R1053H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31154266:31154266(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3152C>T
AA Mutation p.Thr1051Met(p.T1051M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31210098:31210098(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2335A>G
AA Mutation p.Thr779Ala(p.T779A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31130940:31130940(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3892A>G
AA Mutation p.Thr1298Ala(p.T1298A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31182571:31182571(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2737G>T
AA Mutation p.Asp913Tyr(p.D913Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31266879:31266879(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.94C>A
AA Mutation p.Leu32Ile(p.L32I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31225937:31225937(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770550744
CDS Mutation c.1598C>T
AA Mutation p.Thr533Met(p.T533M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31154261:31154261(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144786927
CDS Mutation c.3157C>T
AA Mutation p.Arg1053Cys(p.R1053C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31266314:31266314(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774543132
CDS Mutation c.659C>T
AA Mutation p.Pro220Leu(p.P220L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31120653:31120653(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4491T>G
AA Mutation p.Asp1497Glu(p.D1497E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31251838:31251838(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1315G>A
AA Mutation p.Ala439Thr(p.A439T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31266157:31266157(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.816G>A
AA Mutation p.Met272Ile(p.M272I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31135936:31135936(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3880T>C
AA Mutation p.Phe1294Leu(p.F1294L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31223443:31223443(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781362985
CDS Mutation c.1958G>A
AA Mutation p.Arg653His(p.R653H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31152736:31152736(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148623159
CDS Mutation c.3266C>T
AA Mutation p.Thr1089Met(p.T1089M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31120639:31120639(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4505C>A
AA Mutation p.Thr1502Lys(p.T1502K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31154410:31154410(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3008C>T
AA Mutation p.Ala1003Val(p.A1003V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31210110:31210110(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2323C>A
AA Mutation p.Gln775Lys(p.Q775K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31245592:31245592(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1480G>A
AA Mutation p.Ala494Thr(p.A494T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31120754:31120754(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754307192
CDS Mutation c.4390G>A
AA Mutation p.Ala1464Thr(p.A1464T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31266315:31266315(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.658C>A
AA Mutation p.Pro220Thr(p.P220T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31225916:31225916(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1619C>T
AA Mutation p.Thr540Ile(p.T540I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31223447:31223447(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1954G>T
AA Mutation p.Gly652Cys(p.G652C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31266324:31266324(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.649C>T
AA Mutation p.Arg217Trp(p.R217W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31182538:31182538(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753647509
CDS Mutation c.2770G>A
AA Mutation p.Val924Met(p.V924M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31266934:31266934(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.39T>G
AA Mutation p.Phe13Leu(p.F13L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31135999:31135999(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3817G>A
AA Mutation p.Val1273Met(p.V1273M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31225790:31225790(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1745A>C
AA Mutation p.Lys582Thr(p.K582T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31266179:31266179(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.794C>T
AA Mutation p.Pro265Leu(p.P265L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31202950:31202950(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2451G>A
AA Mutation p.Met817Ile(p.M817I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31252000:31252000(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1153G>A
AA Mutation p.Glu385Lys(p.E385K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31124539:31124539(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749306505
CDS Mutation c.4289C>T
AA Mutation p.Pro1430Leu(p.P1430L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31165003:31165003(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2950C>T
AA Mutation p.Pro984Ser(p.P984S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31245589:31245589(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375094556
CDS Mutation c.1483G>A
AA Mutation p.Val495Ile(p.V495I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31154376:31154376(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3042C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31266313:31266313(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374794029
CDS Mutation c.660G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31223505:31223505(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1896G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31245593:31245593(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773177454
CDS Mutation c.1479C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31127109:31127109(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766297450
CDS Mutation c.4089C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31154340:31154340(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770259428
CDS Mutation c.3078G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31252130:31252130(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755462320
CDS Mutation c.1023C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31182596:31182596(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs187475114
CDS Mutation c.2712C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31266487:31266487(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs182350809
CDS Mutation c.486G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31120719:31120719(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4425C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31120802:31120802(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4342C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31210165:31210165(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200604037
CDS Mutation c.2268C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31266349:31266349(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144719094
CDS Mutation c.624C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence frameshift_variant
Transcription ID ENST00000286827
Start 31245491:31245491(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1581delT
AA Mutation p.Gln528ArgfsTer36(p.Q528Rfs*36)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 51
Mutation Consequence stop_gained
Transcription ID ENST00000286827
Start 31266402:31266402(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.571G>T
AA Mutation p.Glu191Ter(p.E191*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 52
Mutation Consequence stop_gained
Transcription ID ENST00000286827
Start 31266927:31266927(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.46G>T
AA Mutation p.Glu16Ter(p.E16*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 53
Mutation Consequence stop_gained
Transcription ID ENST00000286827
Start 31223579:31223579(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1822G>T
AA Mutation p.Glu608Ter(p.E608*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 54
Mutation Consequence stop_gained
Transcription ID ENST00000286827
Start 31120454:31120454(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4690G>T
AA Mutation p.Gly1564Ter(p.G1564*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 55
Mutation Consequence stop_gained
Transcription ID ENST00000286827
Start 31195296:31195296(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2503G>T
AA Mutation p.Glu835Ter(p.E835*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 56
Mutation Consequence stop_gained
Transcription ID ENST00000286827
Start 31217630:31217630(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2065C>T
AA Mutation p.Arg689Ter(p.R689*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> TIAM1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31213454:31213454(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746654929
CDS Mutation c.2161G>A
AA Mutation p.Glu721Lys(p.E721K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31120659:31120659(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4485G>T
AA Mutation p.Glu1495Asp(p.E1495D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31252014:31252014(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760273681
CDS Mutation c.1139G>A
AA Mutation p.Arg380His(p.R380H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31165059:31165059(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2894G>A
AA Mutation p.Ser965Asn(p.S965N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31266695:31266695(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371530269
CDS Mutation c.278G>A
AA Mutation p.Arg93Gln(p.R93Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31135974:31135974(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770674057
CDS Mutation c.3842C>T
AA Mutation p.Ser1281Leu(p.S1281L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31210164:31210164(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2269G>A
AA Mutation p.Asp757Asn(p.D757N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31266679:31266679(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.294G>T
AA Mutation p.Leu98Phe(p.L98F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000286827
Start 31251829:31251829(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1324G>A
AA Mutation p.Val442Ile(p.V442I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31130241:31130241(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145341566
CDS Mutation c.4017G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31266313:31266313(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374794029
CDS Mutation c.660G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31152735:31152735(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143851539
CDS Mutation c.3267G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31182443:31182443(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765735636
CDS Mutation c.2865C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000286827
Start 31245641:31245641(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763335527
CDS Mutation c.1431C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000286827
Start 31153089:31153089(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3217G>T
AA Mutation p.Glu1073Ter(p.E1073*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000286827
Start 31266445:31266445(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.528G>A
AA Mutation p.Trp176Ter(p.W176*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000286827
Start 31141177:31141177(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3715G>T
AA Mutation p.Glu1239Ter(p.E1239*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript