Mutation

Primary Site >> Stomach Cancer

Gene >> ADAMTS1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26840322:26840322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1619G>A
AA Mutation	p.Cys540Tyr(p.C540Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26838147:26838147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2336T>G
AA Mutation	p.Leu779Arg(p.L779R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26838545:26838545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2098G>A
AA Mutation	p.Gly700Ser(p.G700S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26839607:26839607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2008T>G
AA Mutation	p.Phe670Val(p.F670V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26839914:26839914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1813T>C
AA Mutation	p.Tyr605His(p.Y605H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26837704:26837704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2779G>A
AA Mutation	p.Gly927Ser(p.G927S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26839982:26839982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200821463
CDS Mutation	c.1745C>T
AA Mutation	p.Thr582Met(p.T582M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26837782:26837782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2701A>G
AA Mutation	p.Thr901Ala(p.T901A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26841085:26841085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291G>A
AA Mutation	p.Ala431Thr(p.A431T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000284984
Start	26840060:26840060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142639689
CDS Mutation	c.1667C>T
AA Mutation	p.Thr556Met(p.T556M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26837997:26837997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2486G>A
AA Mutation	p.Gly829Asp(p.G829D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26840293:26840293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648G>A
AA Mutation	p.Asp550Asn(p.D550N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26840379:26840379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1562G>A
AA Mutation	p.Cys521Tyr(p.C521Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26844303:26844303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652G>A
AA Mutation	p.Glu218Lys(p.E218K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26840546:26840546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1395C>A
AA Mutation	p.Asp465Glu(p.D465E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26842517:26842517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770859188
CDS Mutation	c.899A>G
AA Mutation	p.Asn300Ser(p.N300S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26844317:26844317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.638C>T
AA Mutation	p.Thr213Ile(p.T213I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26844593:26844593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362C>A
AA Mutation	p.Ala121Glu(p.A121E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26839601:26839601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2014G>C
AA Mutation	p.Val672Leu(p.V672L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26842594:26842594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26844532:26844532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26838492:26838492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs7278894
CDS Mutation	c.2151C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26844577:26844577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26842642:26842642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26839927:26839927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1800C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000284984
Start	26837692:26837692(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2791delA
AA Mutation	p.Arg931GlufsTer3(p.R931Efs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript