Primary Site >> Stomach Cancer

Gene >> INTS2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000444766
Start 61869078:61869078(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs207476529
CDS Mutation c.3224G>A
AA Mutation p.Ser1075Asn(p.S1075N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000444766
Start 61869082:61869082(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3220C>G
AA Mutation p.Leu1074Val(p.L1074V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000444766
Start 61867991:61867991(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780717831
CDS Mutation c.3287G>A
AA Mutation p.Arg1096Gln(p.R1096Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000444766
Start 61912010:61912010(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749391688
CDS Mutation c.734G>A
AA Mutation p.Arg245His(p.R245H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000444766
Start 61891680:61891680(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1732T>A
AA Mutation p.Tyr578Asn(p.Y578N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000444766
Start 61912011:61912011(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372208858
CDS Mutation c.733C>T
AA Mutation p.Arg245Cys(p.R245C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000444766
Start 61872330:61872330(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2737G>A
AA Mutation p.Val913Ile(p.V913I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000444766
Start 61891592:61891592(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745439048
CDS Mutation c.1820C>T
AA Mutation p.Ala607Val(p.A607V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000444766
Start 61872459:61872459(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2608T>C
AA Mutation p.Cys870Arg(p.C870R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000444766
Start 61895329:61895329(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1573A>T
AA Mutation p.Ile525Phe(p.I525F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000444766
Start 61893890:61893890(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1597G>A
AA Mutation p.Ala533Thr(p.A533T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000444766
Start 61889871:61889871(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1923G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000444766
Start 61872452:61872452(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs753355779
CDS Mutation c.2615delC
AA Mutation p.Pro872HisfsTer2(p.P872Hfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000444766
Start 61881033:61881033(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2252delA
AA Mutation p.Asn751IlefsTer16(p.N751Ifs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000444766
Start 61867978:61867978(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3300delT
AA Mutation p.Phe1100LeufsTer26(p.F1100Lfs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000444766
Start 61867977:61867978(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.3300dupT
AA Mutation p.Met1101TyrfsTer19(p.M1101Yfs*19)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000444766
Start 61891682:61891683(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1729_1730insAAAATAAG
AA Mutation p.Ile577LysfsTer22(p.I577Kfs*22)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript