Colon Cancer: Gene >> ADAMTS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26844522:26844522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.433G>A
AA Mutation	p.Val145Met(p.V145M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26844506:26844506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774133434
CDS Mutation	c.449A>G
AA Mutation	p.Tyr150Cys(p.Y150C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26841909:26841909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374668733
CDS Mutation	c.1159G>A
AA Mutation	p.Val387Ile(p.V387I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26837974:26837974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2509A>G
AA Mutation	p.Lys837Glu(p.K837E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26842526:26842526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.890G>A
AA Mutation	p.Ser297Asn(p.S297N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26837841:26837841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2642G>T
AA Mutation	p.Cys881Phe(p.C881F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26842428:26842428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758996929
CDS Mutation	c.988C>T
AA Mutation	p.Arg330Trp(p.R330W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26842472:26842472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944A>C
AA Mutation	p.Glu315Ala(p.E315A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26844254:26844254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769915069
CDS Mutation	c.701C>T
AA Mutation	p.Pro234Leu(p.P234L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26840434:26840434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1507G>A
AA Mutation	p.Ala503Thr(p.A503T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26838229:26838229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762654704
CDS Mutation	c.2254G>A
AA Mutation	p.Glu752Lys(p.E752K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26842644:26842644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.772C>T
AA Mutation	p.Arg258Cys(p.R258C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26840521:26840521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1420C>A
AA Mutation	p.Pro474Thr(p.P474T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26838487:26838487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2156G>T
AA Mutation	p.Gly719Val(p.G719V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
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

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26837940:26837940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2543C>A
AA Mutation	p.Ser848Tyr(p.S848Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26841952:26841952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116G>T
AA Mutation	p.Met372Ile(p.M372I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26844627:26844627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.328G>A
AA Mutation	p.Gly110Arg(p.G110R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26840366:26840366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1575C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26838071:26838071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2412C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26841053:26841053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26840002:26840002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138109740
CDS Mutation	c.1725C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26844235:26844235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.720A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
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

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26840495:26840495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754926404
CDS Mutation	c.1446C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26844523:26844523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000284984
Start	26841166:26841166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1211-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ADAMTS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26840012:26840012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373807387
CDS Mutation	c.1715C>T
AA Mutation	p.Ser572Leu(p.S572L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26839661:26839661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201769018
CDS Mutation	c.1954G>A
AA Mutation	p.Val652Ile(p.V652I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26842352:26842352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1064T>G
AA Mutation	p.Leu355Arg(p.L355R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284984
Start	26842661:26842661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755G>A
AA Mutation	p.Arg252Gln(p.R252Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284984
Start	26837939:26837939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2544T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000284984
Start	26839923:26839923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1804C>T
AA Mutation	p.Arg602Ter(p.R602*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript