Primary Site >> Stomach Cancer

Gene >> GAS2L3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000266754
Start 100624147:100624147(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1342C>G
AA Mutation p.Pro448Ala(p.P448A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000266754
Start 100624292:100624292(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1487C>A
AA Mutation p.Ser496Tyr(p.S496Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000266754
Start 100624579:100624579(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1774C>G
AA Mutation p.Gln592Glu(p.Q592E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000266754
Start 100623968:100623968(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1163C>T
AA Mutation p.Ser388Leu(p.S388L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000266754
Start 100600415:100600415(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758071152
CDS Mutation c.52C>T
AA Mutation p.Arg18Trp(p.R18W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000266754
Start 100624818:100624818(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2013A>T
AA Mutation p.Lys671Asn(p.K671N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000266754
Start 100612110:100612110(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.414T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000266754
Start 100623915:100623915(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1110T>C
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000266754
Start 100623692:100623692(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.891delA
AA Mutation p.Gly298GlufsTer20(p.G298Efs*20)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000266754
Start 100601643:100601643(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.193A>T
AA Mutation p.Lys65Ter(p.K65*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript