Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KDR

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55125251:55125251(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.43G>A
AA Mutation p.Val15Met(p.V15M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55102005:55102005(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2158C>T
AA Mutation p.Arg720Trp(p.R720W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55098148:55098148(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749143449
CDS Mutation c.2498G>A
AA Mutation p.Arg833Gln(p.R833Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55114880:55114880(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145458680
CDS Mutation c.652G>A
AA Mutation p.Val218Ile(p.V218I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55110732:55110732(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1013C>A
AA Mutation p.Ser338Tyr(p.S338Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55107750:55107750(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1399G>A
AA Mutation p.Ala467Thr(p.A467T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55081994:55081994(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3810A>C
AA Mutation p.Lys1270Asn(p.K1270N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55092621:55092621(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780764266
CDS Mutation c.3065G>A
AA Mutation p.Arg1022Gln(p.R1022Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55092642:55092642(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3044G>A
AA Mutation p.Gly1015Asp(p.G1015D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55098239:55098239(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2407T>C
AA Mutation p.Ser803Pro(p.S803P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55104740:55104740(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1890G>T
AA Mutation p.Lys630Asn(p.K630N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55102428:55102428(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199504669
CDS Mutation c.2068G>A
AA Mutation p.Ala690Thr(p.A690T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55102466:55102466(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200338299
CDS Mutation c.2030C>T
AA Mutation p.Thr677Met(p.T677M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55089984:55089984(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3164A>C
AA Mutation p.Lys1055Thr(p.K1055T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000263923
Start 55098698:55098698(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758102038
CDS Mutation c.2372G>A
AA Mutation p.Arg791Gln(p.R791Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55098711:55098711(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs1139774
CDS Mutation c.2359C>T
AA Mutation p.Arg787Trp(p.R787W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55114235:55114235(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.689C>T
AA Mutation p.Pro230Leu(p.P230L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55094822:55094822(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2951G>T
AA Mutation p.Ser984Ile(p.S984I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55101969:55101969(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747362899
CDS Mutation c.2194G>A
AA Mutation p.Glu732Lys(p.E732K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55113470:55113470(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.810G>T
AA Mutation p.Lys270Asn(p.K270N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55115408:55115408(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.362A>G
AA Mutation p.Tyr121Cys(p.Y121C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55090057:55090057(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3091G>A
AA Mutation p.Ala1031Thr(p.A1031T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55102443:55102443(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374980446
CDS Mutation c.2053G>A
AA Mutation p.Glu685Lys(p.E685K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55114924:55114924(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.608A>C
AA Mutation p.Lys203Thr(p.K203T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55121143:55121143(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.115G>T
AA Mutation p.Asp39Tyr(p.D39Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55106776:55106776(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1447G>A
AA Mutation p.Glu483Lys(p.E483K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55090023:55090023(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3125T>G
AA Mutation p.Val1042Gly(p.V1042G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55118722:55118722(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141577956
CDS Mutation c.240C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55105914:55105914(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200769864
CDS Mutation c.1563G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55081988:55081988(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768623501
CDS Mutation c.3816G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55102417:55102417(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2079T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55082569:55082569(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781436645
CDS Mutation c.3729G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55098775:55098775(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2295C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence frameshift_variant
Transcription ID ENST00000263923
Start 55082586:55082586(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3712delA
AA Mutation p.Thr1238HisfsTer7(p.T1238Hfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 35
Mutation Consequence stop_gained
Transcription ID ENST00000263923
Start 55106743:55106743(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1480G>T
AA Mutation p.Gly494Ter(p.G494*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence stop_gained
Transcription ID ENST00000263923
Start 55089417:55089417(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3361G>T
AA Mutation p.Glu1121Ter(p.E1121*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence stop_gained
Transcription ID ENST00000263923
Start 55088917:55088917(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3461C>A
AA Mutation p.Ser1154Ter(p.S1154*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence stop_gained
Transcription ID ENST00000263923
Start 55089426:55089426(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373654225
CDS Mutation c.3352C>T
AA Mutation p.Arg1118Ter(p.R1118*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence frameshift_variant
Transcription ID ENST00000263923
Start 55110546:55110547(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1111dupC
AA Mutation p.Leu371ProfsTer2(p.L371Pfs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> KDR

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55104680:55104680(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1950G>T
AA Mutation p.Lys650Asn(p.K650N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55118721:55118721(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201719457
CDS Mutation c.241G>A
AA Mutation p.Asp81Asn(p.D81N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55092697:55092697(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764489577
CDS Mutation c.2989A>G
AA Mutation p.Lys997Glu(p.K997E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55113422:55113422(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.858G>T
AA Mutation p.Lys286Asn(p.K286N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55102367:55102367(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2129A>G
AA Mutation p.Asp710Gly(p.D710G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263923
Start 55089434:55089434(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3344T>G
AA Mutation p.Phe1115Cys(p.F1115C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55098787:55098787(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780676775
CDS Mutation c.2283G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55098799:55098799(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2271C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55090046:55090046(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3102C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000263923
Start 55107826:55107826(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1323A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000263923
Start 55082613:55082613(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763426023
CDS Mutation c.3685C>T
AA Mutation p.Arg1229Ter(p.R1229*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript