Mutation

Primary Site >> Stomach Cancer

Gene >> CIITA

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10906985:10906985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1493T>C
AA Mutation	p.Leu498Pro(p.L498P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10907081:10907081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1589C>T
AA Mutation	p.Ala530Val(p.A530V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10922478:10922478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3305T>C
AA Mutation	p.Val1102Ala(p.V1102A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10909052:10909052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143801818
CDS Mutation	c.2681C>T
AA Mutation	p.Ala894Val(p.A894V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10923286:10923286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3376C>T
AA Mutation	p.Arg1126Trp(p.R1126W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10906625:10906625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1133T>C
AA Mutation	p.Leu378Pro(p.L378P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10907007:10907007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1515A>C
AA Mutation	p.Glu505Asp(p.E505D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10922484:10922484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367805896
CDS Mutation	c.3311C>T
AA Mutation	p.Thr1104Met(p.T1104M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10903881:10903881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780678285
CDS Mutation	c.923G>A
AA Mutation	p.Arg308Gln(p.R308Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10907218:10907218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1726G>A
AA Mutation	p.Ala576Thr(p.A576T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10908074:10908074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2582T>C
AA Mutation	p.Leu861Pro(p.L861P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10907869:10907869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2377C>A
AA Mutation	p.Leu793Met(p.L793M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10907870:10907870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2378T>A
AA Mutation	p.Leu793Gln(p.L793Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10907590:10907590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770284013
CDS Mutation	c.2098C>T
AA Mutation	p.Arg700Trp(p.R700W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10895293:10895293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774713571
CDS Mutation	c.64T>C
AA Mutation	p.Cys22Arg(p.C22R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10907650:10907650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2158C>A
AA Mutation	p.Leu720Met(p.L720M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10907176:10907176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199476070
CDS Mutation	c.1684G>A
AA Mutation	p.Ala562Thr(p.A562T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000324288
Start	10907419:10907419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1927G>A
AA Mutation	p.Gly643Ser(p.G643S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324288
Start	10906989:10906989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772143212
CDS Mutation	c.1497C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324288
Start	10906827:10906827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1335C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324288
Start	10907043:10907043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370785250
CDS Mutation	c.1551G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324288
Start	10918482:10918482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3105C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324288
Start	10907073:10907073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1581G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324288
Start	10907448:10907448(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1962delC
AA Mutation	p.Ala656ProfsTer30(p.A656Pfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324288
Start	10906869:10906869(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1381delG
AA Mutation	p.Asp461MetfsTer28(p.D461Mfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript