Primary Site >> Stomach Cancer

Gene >> AURKC

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57232053:57232053(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.125A>G
AA Mutation p.Asp42Gly(p.D42G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
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
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57232067:57232067(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766182833
CDS Mutation c.139C>T
AA Mutation p.Arg47Cys(p.R47C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57231759:57231759(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.76A>G
AA Mutation p.Thr26Ala(p.T26A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57235356:57235356(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.869A>T
AA Mutation p.His290Leu(p.H290L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57235006:57235006(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.707A>T
AA Mutation p.Tyr236Phe(p.Y236F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000302804
Start 57232110:57232110(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.182G>T
AA Mutation p.Arg61Leu(p.R61L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000302804
Start 57232048:57232048(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.120C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000302804
Start 57232561:57232561(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.316C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000302804
Start 57232159:57232159(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.231G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000302804
Start 57235315:57235315(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.828C>A
AA Mutation p.Tyr276Ter(p.Y276*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript