Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LATS1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149684187:149684187(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.902C>A
AA Mutation p.Pro301His(p.P301H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149683312:149683312(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1777A>T
AA Mutation p.Ser593Cys(p.S593C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149701958:149701958(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.169A>G
AA Mutation p.Met57Val(p.M57V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149662153:149662153(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2969G>A
AA Mutation p.Arg990Gln(p.R990Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149676679:149676679(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2652C>A
AA Mutation p.Ser884Arg(p.S884R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149701948:149701948(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.179A>G
AA Mutation p.Glu60Gly(p.E60G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149680099:149680099(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2369T>C
AA Mutation p.Met790Thr(p.M790T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000253339
Start 149683081:149683081(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2008C>T
AA Mutation p.Arg670Trp(p.R670W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149676686:149676686(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2645C>A
AA Mutation p.Pro882His(p.P882H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149695088:149695088(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.482C>T
AA Mutation p.Ala161Val(p.A161V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149661952:149661952(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3170T>C
AA Mutation p.Val1057Ala(p.V1057A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149680237:149680237(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200119992
CDS Mutation c.2231G>A
AA Mutation p.Arg744Gln(p.R744Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149683166:149683166(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs35163691
CDS Mutation c.1923C>A
AA Mutation p.Phe641Leu(p.F641L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000253339
Start 149680338:149680338(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2130A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000253339
Start 149661840:149661840(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750877835
CDS Mutation c.3282G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000253339
Start 149662005:149662005(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3117delT
AA Mutation p.Phe1039LeufsTer19(p.F1039Lfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000253339
Start 149680404:149680404(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2064delA
AA Mutation p.Glu689AsnfsTer18(p.E689Nfs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000253339
Start 149683103:149683103(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1986delA
AA Mutation p.Lys662AsnfsTer3(p.K662Nfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 19
Mutation Consequence stop_gained
Transcription ID ENST00000253339
Start 149680052:149680052(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2416C>T
AA Mutation p.Arg806Ter(p.R806*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence frameshift_variant
Transcription ID ENST00000253339
Start 149680046:149680047(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2421_2422insAATAAAT
AA Mutation p.Tyr808AsnfsTer12(p.Y808Nfs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 21
Mutation Consequence frameshift_variant
Transcription ID ENST00000253339
Start 149684355:149684356(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.733_734insATTCGGGAGA
AA Mutation p.Val245AspfsTer73(p.V245Dfs*73)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 22
Mutation Consequence splice_donor_variant
Transcription ID ENST00000253339
Start 149679873:149679873(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2593+2T>C
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 23
Mutation Consequence protein_altering_variant
Transcription ID ENST00000253339
Start 149680048:149680049(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2419_2420insACA
AA Mutation p.Phe807delinsTyrIle(p.F807delinsYI)
Mutation Classification In_Frame_Ins
Feature Type Transcript

Rectum Cancer: Gene >> LATS1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149684259:149684259(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.830A>G
AA Mutation p.Tyr277Cys(p.Y277C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149662138:149662138(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2984G>A
AA Mutation p.Arg995His(p.R995H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000253339
Start 149662207:149662207(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2915C>T
AA Mutation p.Pro972Leu(p.P972L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000253339
Start 149683901:149683901(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1188T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000253339
Start 149683370:149683370(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772472911
CDS Mutation c.1719C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000253339
Start 149701883:149701883(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 7
Mutation Consequence stop_gained
Transcription ID ENST00000253339
Start 149680259:149680259(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2209C>T
AA Mutation p.Arg737Ter(p.R737*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript