Primary Site >> Stomach Cancer

Gene >> GLI1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000228682
Start 57465224:57465224(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.503C>A
AA Mutation p.Pro168His(p.P168H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000228682
Start 57470368:57470368(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1628G>A
AA Mutation p.Ser543Asn(p.S543N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000228682
Start 57464729:57464729(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.250T>C
AA Mutation p.Ser84Pro(p.S84P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000228682
Start 57470718:57470718(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1978C>A
AA Mutation p.Leu660Met(p.L660M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000228682
Start 57467361:57467361(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373249560
CDS Mutation c.941G>A
AA Mutation p.Arg314His(p.R314H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000228682
Start 57471592:57471592(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2852G>A
AA Mutation p.Gly951Asp(p.G951D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000228682
Start 57464721:57464721(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.242G>A
AA Mutation p.Arg81Gln(p.R81Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000228682
Start 57467346:57467346(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767216717
CDS Mutation c.926G>A
AA Mutation p.Arg309Gln(p.R309Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000228682
Start 57470409:57470409(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201845227
CDS Mutation c.1669C>T
AA Mutation p.Arg557Cys(p.R557C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000228682
Start 57464720:57464720(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753380800
CDS Mutation c.241C>T
AA Mutation p.Arg81Trp(p.R81W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000228682
Start 57470546:57470546(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775573332
CDS Mutation c.1806G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000228682
Start 57471977:57471977(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3237G>C
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000228682
Start 57466292:57466292(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs759448855
CDS Mutation c.821delG
AA Mutation p.Gly274AlafsTer6(p.G274Afs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000228682
Start 57470435:57470435(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1700delC
AA Mutation p.Pro567LeufsTer46(p.P567Lfs*46)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000228682
Start 57470342:57470342(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1607delC
AA Mutation p.Pro536GlnfsTer77(p.P536Qfs*77)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence splice_donor_variant
Transcription ID ENST00000228682
Start 57465257:57465257(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.534+2T>C
Mutation Classification Splice_Site
Feature Type Transcript