Primary Site >> Stomach Cancer

Gene >> ASNS

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000175506
Start 97864280:97864280(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.466G>A
AA Mutation p.Ala156Thr(p.A156T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000175506
Start 97864424:97864424(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.322G>A
AA Mutation p.Gly108Arg(p.G108R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000175506
Start 97869140:97869140(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs398122975
CDS Mutation c.17C>T
AA Mutation p.Ala6Val(p.A6V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000175506
Start 97869011:97869011(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769236847
CDS Mutation c.146G>A
AA Mutation p.Arg49Gln(p.R49Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000175506
Start 97854612:97854612(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1206T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000175506
Start 97859373:97859373(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755945639
CDS Mutation c.513G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000175506
Start 97853120:97853120(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1416T>C
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000175506
Start 97858859:97858859(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.770delT
AA Mutation p.Leu257TyrfsTer15(p.L257Yfs*15)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000175506
Start 97852435:97852435(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1510A>T
AA Mutation p.Lys504Ter(p.K504*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript