Mutation

Primary Site >> Stomach Cancer

Gene >> ITGAD

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31418121:31418121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2546C>A
AA Mutation	p.Pro849His(p.P849H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31411154:31411154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435G>A
AA Mutation	p.Ala479Thr(p.A479T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31414474:31414474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2020T>G
AA Mutation	p.Phe674Val(p.F674V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31412887:31412887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144853512
CDS Mutation	c.1757C>T
AA Mutation	p.Ala586Val(p.A586V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31412949:31412949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1819G>C
AA Mutation	p.Gly607Arg(p.G607R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31394323:31394323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.119T>C
AA Mutation	p.Val40Ala(p.V40A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31394291:31394291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.87G>T
AA Mutation	p.Gln29His(p.Q29H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31411329:31411329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200809631
CDS Mutation	c.1519G>A
AA Mutation	p.Ala507Thr(p.A507T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31423953:31423953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369278071
CDS Mutation	c.3154C>T
AA Mutation	p.Arg1052Cys(p.R1052C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31403596:31403596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751119063
CDS Mutation	c.655G>A
AA Mutation	p.Val219Ile(p.V219I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31423383:31423383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541431535
CDS Mutation	c.2891T>C
AA Mutation	p.Ile964Thr(p.I964T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31416587:31416587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2440A>G
AA Mutation	p.Thr814Ala(p.T814A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31414510:31414510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763655950
CDS Mutation	c.2056C>T
AA Mutation	p.Arg686Cys(p.R686C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000389202
Start	31410817:31410817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1295C>T
AA Mutation	p.Ala432Val(p.A432V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389202
Start	31402185:31402185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746480837
CDS Mutation	c.498T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389202
Start	31394330:31394330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140142659
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389202
Start	31423132:31423132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2799G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389202
Start	31414955:31414955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2247G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000389202
Start	31411328:31411328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770920466
CDS Mutation	c.1518C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389202
Start	31407548:31407548(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.742delA
AA Mutation	p.Ser248ValfsTer53(p.S248Vfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000389202
Start	31410790:31410790(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs772416878
CDS Mutation	c.1273delC
AA Mutation	p.Arg425AlafsTer50(p.R425Afs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000389202
Start	31394234:31394234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.32-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript