Mutation

Primary Site >> Stomach Cancer

Gene >> ITGAX

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31360049:31360049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200320931
CDS Mutation	c.691G>A
AA Mutation	p.Ala231Thr(p.A231T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31359981:31359981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774736704
CDS Mutation	c.623G>A
AA Mutation	p.Arg208His(p.R208H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31371106:31371106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1733C>G
AA Mutation	p.Ser578Cys(p.S578C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31360444:31360444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842T>C
AA Mutation	p.Ile281Thr(p.I281T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31371446:31371446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1954T>C
AA Mutation	p.Ser652Pro(p.S652P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31380015:31380015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762377072
CDS Mutation	c.3010G>A
AA Mutation	p.Ala1004Thr(p.A1004T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31379809:31379809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2921C>A
AA Mutation	p.Pro974His(p.P974H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31362187:31362187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1199T>C
AA Mutation	p.Met400Thr(p.M400T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31363213:31363213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1549C>T
AA Mutation	p.Pro517Ser(p.P517S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31372480:31372480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755857359
CDS Mutation	c.2263G>A
AA Mutation	p.Ala755Thr(p.A755T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31363258:31363258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1594A>C
AA Mutation	p.Asn532His(p.N532H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31371192:31371192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201655601
CDS Mutation	c.1819C>T
AA Mutation	p.Arg607Trp(p.R607W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31361185:31361185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984A>T
AA Mutation	p.Gln328His(p.Q328H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000268296
Start	31377195:31377195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2719C>A
AA Mutation	p.Pro907Thr(p.P907T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268296
Start	31357276:31357276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564218640
CDS Mutation	c.342C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268296
Start	31361864:31361864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138230749
CDS Mutation	c.1041C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268296
Start	31371400:31371400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773833533
CDS Mutation	c.1908G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268296
Start	31372623:31372623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2319C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268296
Start	31380343:31380343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3138C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268296
Start	31372410:31372410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776073190
CDS Mutation	c.2193C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268296
Start	31373261:31373261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2379G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268296
Start	31371739:31371739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2115C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268296
Start	31372428:31372428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2211G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268296
Start	31359788:31359788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759700394
CDS Mutation	c.519C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268296
Start	31381892:31381892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3477G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268296
Start	31362665:31362665(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1276delC
AA Mutation	p.Arg426AlafsTer20(p.R426Afs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268296
Start	31363014:31363014(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1444delC
AA Mutation	p.His482IlefsTer44(p.H482Ifs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000268296
Start	31357039:31357039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.256G>T
AA Mutation	p.Glu86Ter(p.E86*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript