Mutation

Primary Site >> Stomach Cancer

Gene >> CIT

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119718741:119718741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3835C>A
AA Mutation	p.Leu1279Ile(p.L1279I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119752202:119752202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2626C>G
AA Mutation	p.Leu876Val(p.L876V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119712182:119712182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4724A>G
AA Mutation	p.Asp1575Gly(p.D1575G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119712294:119712294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774673206
CDS Mutation	c.4612G>A
AA Mutation	p.Gly1538Arg(p.G1538R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119782558:119782558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1625T>C
AA Mutation	p.Ile542Thr(p.I542T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119767176:119767176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746443265
CDS Mutation	c.2089G>A
AA Mutation	p.Glu697Lys(p.E697K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119690315:119690315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5896C>G
AA Mutation	p.Leu1966Val(p.L1966V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119700763:119700763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749992069
CDS Mutation	c.5479C>T
AA Mutation	p.Arg1827Cys(p.R1827C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119714298:119714298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763529099
CDS Mutation	c.4079A>G
AA Mutation	p.Asn1360Ser(p.N1360S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119752183:119752183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2645C>T
AA Mutation	p.Ser882Phe(p.S882F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119822948:119822948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983C>A
AA Mutation	p.Pro328His(p.P328H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119690428:119690428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5783C>T
AA Mutation	p.Thr1928Met(p.T1928M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119776727:119776727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1781T>G
AA Mutation	p.Leu594Arg(p.L594R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119704421:119704421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5120C>A
AA Mutation	p.Pro1707His(p.P1707H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119834119:119834119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626T>C
AA Mutation	p.Val209Ala(p.V209A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119721368:119721368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773906531
CDS Mutation	c.3547C>T
AA Mutation	p.Arg1183Trp(p.R1183W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119718326:119718326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540727841
CDS Mutation	c.3961C>T
AA Mutation	p.Arg1321Trp(p.R1321W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119718283:119718283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779515686
CDS Mutation	c.4004C>T
AA Mutation	p.Pro1335Leu(p.P1335L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119714310:119714310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774914678
CDS Mutation	c.4067G>A
AA Mutation	p.Arg1356His(p.R1356H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000261833
Start	119704443:119704443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5098C>T
AA Mutation	p.Leu1700Phe(p.L1700F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119772836:119772836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2016G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119708290:119708290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377318034
CDS Mutation	c.4974C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119728508:119728508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3459G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119697682:119697682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5733C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119734196:119734196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747244776
CDS Mutation	c.3192G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119857658:119857658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377141243
CDS Mutation	c.279G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119857610:119857610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.327T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119752233:119752233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748612285
CDS Mutation	c.2595C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119803382:119803382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1119C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261833
Start	119704393:119704393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780981739
CDS Mutation	c.5148C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261833
Start	119690285:119690285(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5926delC
AA Mutation	p.Leu1976TrpfsTer36(p.L1976Wfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000261833
Start	119735189:119735189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3001C>T
AA Mutation	p.Arg1001Ter(p.R1001*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000261833
Start	119712696:119712696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4454-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	34
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000261833
Start	119690227:119690262(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.5949_5984delCCGGATGCTCAGCACGCGGAGAGAGCGGTCCCCCGG
AA Mutation	p.Met1985_Arg1996del(p.M1985_R1996del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript