Primary Site >> Stomach Cancer

Gene >> ILK

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000299421
Start 6608952:6608952(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.517A>G
AA Mutation p.Thr173Ala(p.T173A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000299421
Start 6610003:6610003(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377094824
CDS Mutation c.1046G>A
AA Mutation p.Arg349His(p.R349H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000299421
Start 6608788:6608788(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.446G>A
AA Mutation p.Arg149Gln(p.R149Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000299421
Start 6609601:6609601(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774113906
CDS Mutation c.818C>T
AA Mutation p.Pro273Leu(p.P273L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000299421
Start 6608158:6608158(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.202G>A
AA Mutation p.Asp68Asn(p.D68N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000299421
Start 6609554:6609554(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.771C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000299421
Start 6608162:6608162(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.211delC
AA Mutation p.Leu71CysfsTer26(p.L71Cfs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000299421
Start 6608462:6608462(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.328delT
AA Mutation p.Trp110GlyfsTer35(p.W110Gfs*35)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000299421
Start 6608062:6608063(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.111dupC
AA Mutation p.His39AlafsTer13(p.H39Afs*13)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000299421
Start 6604357:6604358(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.89+1dupG
Mutation Classification Frame_Shift_Ins
Feature Type Transcript