Primary Site >> Stomach Cancer

Gene >> IVNS1ABP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000367498
Start 185300996:185300996(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1096A>G
AA Mutation p.Met366Val(p.M366V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000367498
Start 185298121:185298121(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764078356
CDS Mutation c.1843G>A
AA Mutation p.Asp615Asn(p.D615N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000367498
Start 185307581:185307581(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.439T>C
AA Mutation p.Ser147Pro(p.S147P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000367498
Start 185307640:185307640(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.380C>A
AA Mutation p.Ser127Tyr(p.S127Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000367498
Start 185301049:185301049(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1043A>G
AA Mutation p.Glu348Gly(p.E348G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000367498
Start 185298099:185298099(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1865C>T
AA Mutation p.Thr622Met(p.T622M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000367498
Start 185308811:185308811(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.346C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000367498
Start 185308824:185308825(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.332dupA
AA Mutation p.Leu112AlafsTer12(p.L112Afs*12)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000367498
Start 185309113:185309114(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.169_170dupTT
AA Mutation p.Leu57PhefsTer32(p.L57Ffs*32)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript