Mutation

Primary Site >> Stomach Cancer

Gene >> ITGAL

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356798
Start	30494791:30494791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444G>A
AA Mutation	p.Ala482Thr(p.A482T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356798
Start	30521561:30521561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3409G>A
AA Mutation	p.Ala1137Thr(p.A1137T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356798
Start	30496190:30496190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530715206
CDS Mutation	c.1597G>A
AA Mutation	p.Gly533Ser(p.G533S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356798
Start	30496559:30496559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750373265
CDS Mutation	c.1825G>A
AA Mutation	p.Val609Met(p.V609M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356798
Start	30511103:30511103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2753C>A
AA Mutation	p.Pro918His(p.P918H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356798
Start	30496193:30496193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561225020
CDS Mutation	c.1600G>A
AA Mutation	p.Asp534Asn(p.D534N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356798
Start	30484137:30484137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.880G>A
AA Mutation	p.Glu294Lys(p.E294K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356798
Start	30494215:30494215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1217A>G
AA Mutation	p.Tyr406Cys(p.Y406C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356798
Start	30494238:30494238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551557846
CDS Mutation	c.1240C>T
AA Mutation	p.Arg414Trp(p.R414W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356798
Start	30475310:30475310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781453504
CDS Mutation	c.169A>G
AA Mutation	p.Ile57Val(p.I57V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000356798
Start	30496487:30496487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1753A>T
AA Mutation	p.Ile585Phe(p.I585F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000356798
Start	30510454:30510454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2602T>G
AA Mutation	p.Phe868Val(p.F868V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356798
Start	30518671:30518671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3180C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356798
Start	30510924:30510924(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2668delG
AA Mutation	p.Asp890ThrfsTer9(p.D890Tfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356798
Start	30506817:30506817(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2474delC
AA Mutation	p.Pro825ArgfsTer11(p.P825Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356798
Start	30504197:30504197(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2172delC
AA Mutation	p.Ile725SerfsTer5(p.I725Sfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000356798
Start	30496550:30496550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1816C>T
AA Mutation	p.Gln606Ter(p.Q606*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356798
Start	30517011:30517012(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2902dupA
AA Mutation	p.Thr968AsnfsTer34(p.T968Nfs*34)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	19
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000356798
Start	30521517:30521519(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3367_3369delGAG
AA Mutation	p.Glu1123del(p.E1123del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript