Mutation

Primary Site >> Stomach Cancer

Gene >> ITGAV

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261023
Start	186656331:186656331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1649G>A
AA Mutation	p.Ser550Asn(p.S550N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261023
Start	186677249:186677249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3104A>G
AA Mutation	p.Gln1035Arg(p.Q1035R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261023
Start	186656298:186656298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771409986
CDS Mutation	c.1616G>A
AA Mutation	p.Arg539Gln(p.R539Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261023
Start	186659047:186659047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1729G>A
AA Mutation	p.Glu577Lys(p.E577K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261023
Start	186625568:186625568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.504G>T
AA Mutation	p.Glu168Asp(p.E168D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261023
Start	186675823:186675823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757331033
CDS Mutation	c.2824G>A
AA Mutation	p.Glu942Lys(p.E942K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261023
Start	186637079:186637079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772G>A
AA Mutation	p.Val258Ile(p.V258I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261023
Start	186668846:186668846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2518T>C
AA Mutation	p.Tyr840His(p.Y840H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261023
Start	186659092:186659092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200949549
CDS Mutation	c.1774C>T
AA Mutation	p.Arg592Trp(p.R592W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261023
Start	186666714:186666714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2177G>C
AA Mutation	p.Gly726Ala(p.G726A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261023
Start	186602121:186602121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200516634
CDS Mutation	c.286C>T
AA Mutation	p.Arg96Trp(p.R96W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261023
Start	186641534:186641534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1105C>T
AA Mutation	p.Arg369Trp(p.R369W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261023
Start	186656257:186656257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1575G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261023
Start	186669799:186669799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2691A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261023
Start	186676848:186676848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140775791
CDS Mutation	c.2964G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261023
Start	186656358:186656358(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1682delG
AA Mutation	p.Gly561AspfsTer2(p.G561Dfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261023
Start	186675682:186675682(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2785delG
AA Mutation	p.Val929Ter(p.V929*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261023
Start	186590473:186590474(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.136_137delGG
AA Mutation	p.Gly46LysfsTer44(p.G46Kfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000261023
Start	186656297:186656297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1615C>T
AA Mutation	p.Arg539Ter(p.R539*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000261023
Start	186638286:186638286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812C>A
AA Mutation	p.Ser271Ter(p.S271*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261023
Start	186656357:186656358(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1682dupG
AA Mutation	p.Leu562ThrfsTer5(p.L562Tfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261023
Start	186625518:186625519(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.458_459dupAG
AA Mutation	p.Pro154SerfsTer86(p.P154Sfs*86)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	23
Mutation Consequence	splice_donor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000261023
Start	186590466:186590533(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.130_185+12delCCCGAGGGAAGTTACTTCGGCTTCGCCGTGGATTTCTTCGTGCCCAGCGCGTCTTCGTAAGTGGCCGC
Mutation Classification	Splice_Site
Feature Type	Transcript