Primary Site >> Stomach Cancer

Gene >> IRS1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226795497:226795497(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372681714
CDS Mutation c.3242G>A
AA Mutation p.Arg1081His(p.R1081H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226798615:226798615(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.124G>A
AA Mutation p.Ala42Thr(p.A42T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226797588:226797588(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1151C>A
AA Mutation p.Pro384His(p.P384H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226797726:226797726(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1013G>A
AA Mutation p.Arg338His(p.R338H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226796350:226796350(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2389C>T
AA Mutation p.Arg797Cys(p.R797C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226797673:226797673(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773817315
CDS Mutation c.1066G>A
AA Mutation p.Ala356Thr(p.A356T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226795474:226795474(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781408207
CDS Mutation c.3265C>T
AA Mutation p.Arg1089Cys(p.R1089C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226797180:226797180(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1559G>A
AA Mutation p.Arg520Gln(p.R520Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226797573:226797573(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1166C>T
AA Mutation p.Pro389Leu(p.P389L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226798344:226798344(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.395G>A
AA Mutation p.Gly132Asp(p.G132D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226797547:226797547(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1192A>G
AA Mutation p.Ser398Gly(p.S398G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226798614:226798614(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.125C>T
AA Mutation p.Ala42Val(p.A42V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226796308:226796308(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2431A>G
AA Mutation p.Thr811Ala(p.T811A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000305123
Start 226796173:226796173(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2566G>A
AA Mutation p.Ala856Thr(p.A856T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000305123
Start 226798337:226798337(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.402C>T
Mutation Classification Silent
Feature Type Transcript
ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000305123
Start 226795358:226795358(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs533260174
CDS Mutation c.3381C>T
Mutation Classification Silent
Feature Type Transcript
ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000305123
Start 226795538:226795538(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3201G>A
Mutation Classification Silent
Feature Type Transcript
ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000305123
Start 226797494:226797494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1245G>A
Mutation Classification Silent
Feature Type Transcript
ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000305123
Start 226795211:226795211(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3528T>C
Mutation Classification Silent
Feature Type Transcript
ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000305123
Start 226796636:226796636(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772248279
CDS Mutation c.2103C>T
Mutation Classification Silent
Feature Type Transcript
ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000305123
Start 226797317:226797317(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1422C>T
Mutation Classification Silent
Feature Type Transcript
ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000305123
Start 226797953:226797953(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.786T>C
Mutation Classification Silent
Feature Type Transcript
ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000305123
Start 226798364:226798364(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.375G>A
Mutation Classification Silent
Feature Type Transcript
ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000305123
Start 226796225:226796225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2514G>A
Mutation Classification Silent
Feature Type Transcript
ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000305123
Start 226797812:226797812(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757476072
CDS Mutation c.927C>T
Mutation Classification Silent
Feature Type Transcript
ID 26
Mutation Consequence frameshift_variant
Transcription ID ENST00000305123
Start 226797636:226797636(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1103delC
AA Mutation p.Pro368ArgfsTer95(p.P368Rfs*95)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 27
Mutation Consequence frameshift_variant
Transcription ID ENST00000305123
Start 226796625:226796625(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2114delG
AA Mutation p.Gly705AlafsTer29(p.G705Afs*29)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 28
Mutation Consequence frameshift_variant
Transcription ID ENST00000305123
Start 226795554:226795554(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3185delG
AA Mutation p.Gly1062AlafsTer8(p.G1062Afs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 29
Mutation Consequence frameshift_variant
Transcription ID ENST00000305123
Start 226796501:226796501(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2238delC
AA Mutation p.Ser747ProfsTer196(p.S747Pfs*196)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 30
Mutation Consequence frameshift_variant
Transcription ID ENST00000305123
Start 226795125:226795125(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3614delC
AA Mutation p.Pro1205HisfsTer22(p.P1205Hfs*22)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 31
Mutation Consequence frameshift_variant
Transcription ID ENST00000305123
Start 226797479:226797479(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1260delC
AA Mutation p.Ser421AlafsTer42(p.S421Afs*42)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 32
Mutation Consequence frameshift_variant
Transcription ID ENST00000305123
Start 226795131:226795131(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3608delC
AA Mutation p.Pro1203HisfsTer24(p.P1203Hfs*24)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 33
Mutation Consequence stop_gained
Transcription ID ENST00000305123
Start 226798024:226798024(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.715C>T
AA Mutation p.Gln239Ter(p.Q239*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 34
Mutation Consequence stop_gained
Transcription ID ENST00000305123
Start 226797835:226797835(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.904C>T
AA Mutation p.Arg302Ter(p.R302*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 35
Mutation Consequence frameshift_variant
Transcription ID ENST00000305123
Start 226796955:226796956(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1783_1784insT
AA Mutation p.Arg595LeufsTer16(p.R595Lfs*16)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript