Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FLT4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180616464:180616464(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3122G>A
AA Mutation p.Arg1041Gln(p.R1041Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180630229:180630229(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754692331
CDS Mutation c.509G>A
AA Mutation p.Arg170His(p.R170H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180611349:180611349(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373742042
CDS Mutation c.3668G>A
AA Mutation p.Arg1223His(p.R1223H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180620299:180620299(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2416G>A
AA Mutation p.Ala806Thr(p.A806T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180616449:180616449(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3137C>T
AA Mutation p.Ser1046Leu(p.S1046L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180620888:180620888(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2287G>A
AA Mutation p.Val763Met(p.V763M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180609041:180609041(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3820G>T
AA Mutation p.Asp1274Tyr(p.D1274Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180620665:180620665(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757057248
CDS Mutation c.2350G>A
AA Mutation p.Val784Ile(p.V784I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180614117:180614117(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3282G>C
AA Mutation p.Gln1094His(p.Q1094H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180616377:180616377(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3209G>T
AA Mutation p.Arg1070Leu(p.R1070L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180610000:180610000(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766960409
CDS Mutation c.3712G>A
AA Mutation p.Gly1238Arg(p.G1238R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180609991:180609991(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3721G>T
AA Mutation p.Ala1241Ser(p.A1241S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180626259:180626259(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1110G>T
AA Mutation p.Lys370Asn(p.K370N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180621632:180621632(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1930G>A
AA Mutation p.Ala644Thr(p.A644T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180616378:180616378(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3208C>A
AA Mutation p.Arg1070Ser(p.R1070S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180616408:180616408(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778806900
CDS Mutation c.3178C>T
AA Mutation p.Arg1060Trp(p.R1060W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180621610:180621610(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1952A>G
AA Mutation p.Tyr651Cys(p.Y651C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180629728:180629728(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.784G>A
AA Mutation p.Val262Ile(p.V262I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180624053:180624053(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755736057
CDS Mutation c.1430G>A
AA Mutation p.Arg477Gln(p.R477Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180622754:180622754(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768195465
CDS Mutation c.1634G>A
AA Mutation p.Arg545Gln(p.R545Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180621868:180621868(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1694C>T
AA Mutation p.Ser565Phe(p.S565F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000261937
Start 180603222:180603222(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762533367
CDS Mutation c.4062C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000261937
Start 180620231:180620231(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2484C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000261937
Start 180616409:180616409(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3177C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000261937
Start 180630643:180630643(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757182081
CDS Mutation c.312C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000261937
Start 180621759:180621759(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764502895
CDS Mutation c.1803G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000261937
Start 180619293:180619293(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2721C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000261937
Start 180630082:180630082(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752883158
CDS Mutation c.537C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000261937
Start 180614138:180614138(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150040385
CDS Mutation c.3261C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000261937
Start 180621714:180621714(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs34303265
CDS Mutation c.1848C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence frameshift_variant
Transcription ID ENST00000261937
Start 180631748:180631748(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.89delC
AA Mutation p.Pro30ArgfsTer3(p.P30Rfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 32
Mutation Consequence stop_gained
Transcription ID ENST00000261937
Start 180630711:180630711(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.244C>T
AA Mutation p.Arg82Ter(p.R82*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence frameshift_variant
Transcription ID ENST00000261937
Start 180631747:180631748(version: GRCh38)
Mutation Type INS
dbSNP_RS rs755445139
CDS Mutation c.89dupC
AA Mutation p.Thr31AspfsTer15(p.T31Dfs*15)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000261937
Start 180603231:180603232(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.4052dupC
AA Mutation p.Ser1352ValfsTer92(p.S1352Vfs*92)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 35
Mutation Consequence splice_donor_variant
Transcription ID ENST00000261937
Start 180625868:180625868(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1421+1G>A
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> FLT4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180614137:180614137(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3262G>A
AA Mutation p.Asp1088Asn(p.D1088N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180619304:180619304(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2710G>A
AA Mutation p.Gly904Ser(p.G904S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000261937
Start 180630235:180630235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.503C>G
AA Mutation p.Thr168Arg(p.T168R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000261937
Start 180620687:180620687(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139263798
CDS Mutation c.2328C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000261937
Start 180629269:180629269(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.975C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000261937
Start 180618831:180618831(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2940C>T
Mutation Classification Silent
Feature Type Transcript