Mutation

Primary Site >> Stomach Cancer

Gene >> ADAMTS2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179124998:179124998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201998372
CDS Mutation	c.2933G>A
AA Mutation	p.Arg978His(p.R978H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179113984:179113984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3519A>C
AA Mutation	p.Glu1173Asp(p.E1173D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179114285:179114285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3218T>C
AA Mutation	p.Met1073Thr(p.M1073T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179135958:179135958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144554943
CDS Mutation	c.2036G>A
AA Mutation	p.Arg679His(p.R679H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179130041:179130041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2348C>A
AA Mutation	p.Ala783Asp(p.A783D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179207557:179207557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376856341
CDS Mutation	c.847G>A
AA Mutation	p.Gly283Arg(p.G283R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179154082:179154082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752634323
CDS Mutation	c.1349G>A
AA Mutation	p.Arg450His(p.R450H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179114024:179114024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3479C>T
AA Mutation	p.Ala1160Val(p.A1160V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179130055:179130055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2334G>T
AA Mutation	p.Glu778Asp(p.E778D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179343783:179343783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518G>A
AA Mutation	p.Ser173Asn(p.S173N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179207643:179207643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761G>C
AA Mutation	p.Arg254Thr(p.R254T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179153612:179153612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1394G>A
AA Mutation	p.Cys465Tyr(p.C465Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179158752:179158752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146441575
CDS Mutation	c.1103G>A
AA Mutation	p.Arg368Gln(p.R368Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179158753:179158753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371384169
CDS Mutation	c.1102C>T
AA Mutation	p.Arg368Trp(p.R368W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179181110:179181110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535377243
CDS Mutation	c.937G>A
AA Mutation	p.Val313Met(p.V313M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179272924:179272924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675G>T
AA Mutation	p.Gln225His(p.Q225H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179272970:179272970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629T>C
AA Mutation	p.Val210Ala(p.V210A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000251582
Start	179130096:179130096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777314559
CDS Mutation	c.2293G>A
AA Mutation	p.Val765Ile(p.V765I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179125038:179125038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144138766
CDS Mutation	c.2893G>A
AA Mutation	p.Glu965Lys(p.E965K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179343984:179343984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.317G>A
AA Mutation	p.Gly106Asp(p.G106D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179113886:179113886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3617A>T
AA Mutation	p.Glu1206Val(p.E1206V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179114013:179114013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776115866
CDS Mutation	c.3490C>T
AA Mutation	p.Pro1164Ser(p.P1164S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000251582
Start	179344113:179344113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.188G>A
AA Mutation	p.Arg63His(p.R63H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179136002:179136002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1992C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179128065:179128065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2511T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179154819:179154819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179158790:179158790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1065C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179129974:179129974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2415G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179181105:179181105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.942C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179113987:179113987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3516T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179121683:179121683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763966576
CDS Mutation	c.3156G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179273026:179273026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774498509
CDS Mutation	c.573C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179343845:179343845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750739595
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179128035:179128035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2541C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179125048:179125048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370397254
CDS Mutation	c.2883C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179272957:179272957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.642G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251582
Start	179344082:179344082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251582
Start	179272930:179272930(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.669delG
AA Mutation	p.Pro224HisfsTer23(p.P224Hfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000251582
Start	179128090:179128090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2486C>A
AA Mutation	p.Ser829Ter(p.S829*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000251582
Start	179132312:179132312(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2210-2delA
Mutation Classification	Splice_Site
Feature Type	Transcript