Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SCUBE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000520467
Start	9021166:9021166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2795T>C
AA Mutation	p.Val932Ala(p.V932A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000520467
Start	9030838:9030838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2090G>A
AA Mutation	p.Arg697Gln(p.R697Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000520467
Start	9027441:9027441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370883793
CDS Mutation	c.2453G>A
AA Mutation	p.Arg818His(p.R818H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000520467
Start	9059369:9059369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147079601
CDS Mutation	c.1024G>A
AA Mutation	p.Val342Met(p.V342M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000520467
Start	9047437:9047437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1921G>A
AA Mutation	p.Val641Met(p.V641M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000520467
Start	9059303:9059303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090G>T
AA Mutation	p.Asp364Tyr(p.D364Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000520467
Start	9029902:9029902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2314A>G
AA Mutation	p.Asn772Asp(p.N772D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000520467
Start	9047532:9047532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756925394
CDS Mutation	c.1826G>A
AA Mutation	p.Arg609Gln(p.R609Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000520467
Start	9025798:9025798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138426692
CDS Mutation	c.2587G>A
AA Mutation	p.Ala863Thr(p.A863T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520467
Start	9025760:9025760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2625C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520467
Start	9029924:9029924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771636204
CDS Mutation	c.2292G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520467
Start	9053142:9053142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145459189
CDS Mutation	c.1404C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520467
Start	9066806:9066806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.651T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520467
Start	9025814:9025814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2571C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520467
Start	9027518:9027518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2376T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520467
Start	9025799:9025799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534458521
CDS Mutation	c.2586C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520467
Start	9027431:9027431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139856572
CDS Mutation	c.2463C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520467
Start	9047441:9047441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370455985
CDS Mutation	c.1917C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520467
Start	9079422:9079423(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.343_344delGA
AA Mutation	p.Asp115TrpfsTer7(p.D115Wfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000520467
Start	9065978:9065978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760063339
CDS Mutation	c.763C>T
AA Mutation	p.Arg255Ter(p.R255*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520467
Start	9029954:9029955(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2261dupA
AA Mutation	p.Asn754LysfsTer2(p.N754Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000520467
Start	9055910:9055910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1091-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> SCUBE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000520467
Start	9027419:9027419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2475G>T
AA Mutation	p.Glu825Asp(p.E825D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000520467
Start	9079437:9079437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751243340
CDS Mutation	c.329G>A
AA Mutation	p.Arg110His(p.R110H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000520467
Start	9029953:9029953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2263A>G
AA Mutation	p.Asn755Asp(p.N755D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000520467
Start	9047527:9047527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1831G>A
AA Mutation	p.Glu611Lys(p.E611K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520467
Start	9079445:9079445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.321C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520467
Start	9074587:9074587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368262750
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000520467
Start	9074527:9074527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.471G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520467
Start	9079499:9079499(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.267delA
AA Mutation	p.Glu89AspfsTer15(p.E89Dfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript