Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> AURKC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57235260:57235260(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.773T>G
AA Mutation p.Phe258Cys(p.F258C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57232653:57232653(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.408G>T
AA Mutation p.Glu136Asp(p.E136D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57231294:57231294(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs182340558
CDS Mutation c.46G>T
AA Mutation p.Ala16Ser(p.A16S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57232558:57232558(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756195705
CDS Mutation c.313C>T
AA Mutation p.Arg105Cys(p.R105C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57232670:57232670(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781321656
CDS Mutation c.425G>A
AA Mutation p.Arg142His(p.R142H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57235380:57235380(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs575228273
CDS Mutation c.893G>A
AA Mutation p.Arg298Gln(p.R298Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000302804
Start 57232679:57232679(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs45503793
CDS Mutation c.434C>T
AA Mutation p.Thr145Met(p.T145M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000302804
Start 57232039:57232039(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.111C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000302804
Start 57235279:57235279(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.796delG
AA Mutation p.Ala266ProfsTer4(p.A266Pfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> AURKC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57232573:57232573(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.328T>G
AA Mutation p.Phe110Val(p.F110V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57232158:57232158(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.230C>T
AA Mutation p.Ser77Leu(p.S77L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57232068:57232068(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs137858773
CDS Mutation c.140G>A
AA Mutation p.Arg47His(p.R47H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57232197:57232197(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.269G>T
AA Mutation p.Arg90Leu(p.R90L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57234929:57234929(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.630G>T
AA Mutation p.Met210Ile(p.M210I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57232194:57232194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.266G>A
AA Mutation p.Arg89His(p.R89H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000302804
Start 57232063:57232063(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760247885
CDS Mutation c.135C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000302804
Start 57232039:57232039(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.111C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence splice_donor_variant
Transcription ID ENST00000302804
Start 57231789:57231789(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.104+2T>C
Mutation Classification Splice_Site
Feature Type Transcript