Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ULK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131916470:131916470(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs565402146
CDS Mutation c.1951G>A
AA Mutation p.Val651Met(p.V651M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131920084:131920084(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369823883
CDS Mutation c.2909G>A
AA Mutation p.Arg970His(p.R970H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131916428:131916428(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1909C>A
AA Mutation p.Pro637Thr(p.P637T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131895656:131895656(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.167C>A
AA Mutation p.Ser56Tyr(p.S56Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131908700:131908700(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.373G>A
AA Mutation p.Ala125Thr(p.A125T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131911990:131911990(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.997G>C
AA Mutation p.Asp333His(p.D333H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131909941:131909941(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.748C>T
AA Mutation p.Pro250Ser(p.P250S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131919269:131919269(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773571100
CDS Mutation c.2569G>A
AA Mutation p.Val857Ile(p.V857I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131908736:131908736(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.409C>T
AA Mutation p.Arg137Cys(p.R137C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131909931:131909931(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.738G>T
AA Mutation p.Glu246Asp(p.E246D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131919477:131919477(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770028247
CDS Mutation c.2690C>T
AA Mutation p.Ala897Val(p.A897V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131910290:131910290(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.845C>A
AA Mutation p.Pro282His(p.P282H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000321867
Start 131921120:131921120(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371996516
CDS Mutation c.2982C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000321867
Start 131908914:131908914(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.507G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000321867
Start 131918612:131918612(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2442C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000321867
Start 131917016:131917016(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140491730
CDS Mutation c.2136G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000321867
Start 131913217:131913217(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757968994
CDS Mutation c.1116G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000321867
Start 131921219:131921219(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138011167
CDS Mutation c.3081C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000321867
Start 131921337:131921337(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs117577371
CDS Mutation c.3129G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000321867
Start 131919556:131919556(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143340589
CDS Mutation c.2769C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence frameshift_variant
Transcription ID ENST00000321867
Start 131917521:131917521(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2299delC
AA Mutation p.Gln767ArgfsTer57(p.Q767Rfs*57)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 22
Mutation Consequence frameshift_variant
Transcription ID ENST00000321867
Start 131915998:131915998(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1722delC
AA Mutation p.Thr575ArgfsTer72(p.T575Rfs*72)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 23
Mutation Consequence frameshift_variant
Transcription ID ENST00000321867
Start 131910259:131910259(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.819delT
AA Mutation p.His274IlefsTer109(p.H274Ifs*109)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 24
Mutation Consequence frameshift_variant
Transcription ID ENST00000321867
Start 131916426:131916426(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1911delC
AA Mutation p.Ser638AlafsTer9(p.S638Afs*9)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 25
Mutation Consequence frameshift_variant
Transcription ID ENST00000321867
Start 131919313:131919313(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2618delG
AA Mutation p.Gly873AlafsTer18(p.G873Afs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 26
Mutation Consequence splice_donor_variant
Transcription ID ENST00000321867
Start 131909834:131909834(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.725+1G>A
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> ULK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000321867
Start 131916088:131916088(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142452051
CDS Mutation c.1807C>T
AA Mutation p.Arg603Trp(p.R603W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000321867
Start 131917038:131917038(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2158C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 3
Mutation Consequence stop_lost
Transcription ID ENST00000321867
Start 131921359:131921359(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3151T>G
AA Mutation p.Ter1051GlyextTer36(p.*1051Gext*36)
Mutation Classification Nonstop_Mutation
Feature Type Transcript