Mutation

Primary Site >> Stomach Cancer

Gene >> SETD1A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30979649:30979649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772555919
CDS Mutation	c.3863G>A
AA Mutation	p.Arg1288His(p.R1288H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30979331:30979331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3545C>G
AA Mutation	p.Pro1182Arg(p.P1182R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30979823:30979823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778079685
CDS Mutation	c.4037C>T
AA Mutation	p.Ala1346Val(p.A1346V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30980782:30980782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755261245
CDS Mutation	c.4625G>A
AA Mutation	p.Arg1542Gln(p.R1542Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30964821:30964821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1079G>A
AA Mutation	p.Arg360His(p.R360H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30964674:30964674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764044469
CDS Mutation	c.932G>A
AA Mutation	p.Arg311His(p.R311H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30965127:30965127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1385C>A
AA Mutation	p.Pro462Gln(p.P462Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30964916:30964916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771871764
CDS Mutation	c.1174C>A
AA Mutation	p.Pro392Thr(p.P392T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30966003:30966003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2122G>A
AA Mutation	p.Gly708Ser(p.G708S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30971437:30971437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3076G>A
AA Mutation	p.Glu1026Lys(p.E1026K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30964814:30964814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1072C>G
AA Mutation	p.Gln358Glu(p.Q358E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30980116:30980116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750790917
CDS Mutation	c.4330C>T
AA Mutation	p.Arg1444Trp(p.R1444W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30965124:30965124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382G>A
AA Mutation	p.Arg461His(p.R461H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262519
Start	30964724:30964724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201145470
CDS Mutation	c.982G>A
AA Mutation	p.Ala328Thr(p.A328T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262519
Start	30959147:30959147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.207C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262519
Start	30979635:30979635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570770215
CDS Mutation	c.3849G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262519
Start	30965807:30965807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777902844
CDS Mutation	c.1926G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262519
Start	30971505:30971505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3144G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262519
Start	30981141:30981141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532298159
CDS Mutation	c.4773C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262519
Start	30979323:30979323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200527523
CDS Mutation	c.3537G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262519
Start	30964990:30964990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1248G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262519
Start	30971502:30971502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3141C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262519
Start	30971625:30971625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370157586
CDS Mutation	c.3264G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262519
Start	30979737:30979737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3951C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262519
Start	30965996:30965996(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2121delC
AA Mutation	p.Gly708ValfsTer95(p.G708Vfs*95)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262519
Start	30964916:30964916(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1178delC
AA Mutation	p.Pro393LeufsTer104(p.P393Lfs*104)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262519
Start	30964253:30964253(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.799delT
AA Mutation	p.Ser267ProfsTer230(p.S267Pfs*230)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262519
Start	30964176:30964176(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.726delC
AA Mutation	p.Cys243AlafsTer254(p.C243Afs*254)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262519
Start	30966039:30966039(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2162delC
AA Mutation	p.Pro721ArgfsTer82(p.P721Rfs*82)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262519
Start	30979713:30979714(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3932dupC
AA Mutation	p.Ala1312CysfsTer22(p.A1312Cfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	31
Mutation Consequence	start_lost
Transcription ID	ENST00000262519
Start	30958733:30958733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript