Colon Cancer: Gene >> ADAMTS15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130469370:130469370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755197416
CDS Mutation	c.1651G>A
AA Mutation	p.Gly551Arg(p.G551R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130473532:130473532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2564G>A
AA Mutation	p.Cys855Tyr(p.C855Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130449327:130449327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.354C>A
AA Mutation	p.Ser118Arg(p.S118R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130473410:130473410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2442C>A
AA Mutation	p.Asp814Glu(p.D814E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130473421:130473421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2453C>A
AA Mutation	p.Pro818His(p.P818H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130462686:130462686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189029139
CDS Mutation	c.1448G>A
AA Mutation	p.Arg483His(p.R483H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130462598:130462598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535808287
CDS Mutation	c.1360G>A
AA Mutation	p.Val454Met(p.V454M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130462560:130462560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322G>T
AA Mutation	p.Ser441Ile(p.S441I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130462150:130462150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154G>A
AA Mutation	p.Arg385Gln(p.R385Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130473526:130473526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765064754
CDS Mutation	c.2558C>T
AA Mutation	p.Ala853Val(p.A853V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130449716:130449716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759898564
CDS Mutation	c.743C>T
AA Mutation	p.Thr248Met(p.T248M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299164
Start	130449507:130449507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299164
Start	130469369:130469369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373357559
CDS Mutation	c.1650C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299164
Start	130462720:130462720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199807884
CDS Mutation	c.1482C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299164
Start	130461581:130461581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765014170
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ADAMTS15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130462192:130462192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200077954
CDS Mutation	c.1196G>A
AA Mutation	p.Arg399His(p.R399H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299164
Start	130471303:130471303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1998G>T
AA Mutation	p.Lys666Asn(p.K666N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299164
Start	130449378:130449378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.405C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299164
Start	130469429:130469429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1710C>T
Mutation Classification	Silent
Feature Type	Transcript