Colon Cancer: Gene >> COPS6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303904
Start	100089725:100089725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313T>C
AA Mutation	p.Tyr105His(p.Y105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303904
Start	100090607:100090607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439G>A
AA Mutation	p.Glu147Lys(p.E147K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303904
Start	100091095:100091095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.592A>T
AA Mutation	p.Ile198Phe(p.I198F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303904
Start	100091310:100091310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722A>T
AA Mutation	p.Tyr241Phe(p.Y241F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303904
Start	100090640:100090640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.472A>C
AA Mutation	p.Thr158Pro(p.T158P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303904
Start	100091710:100091710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749647179
CDS Mutation	c.905T>C
AA Mutation	p.Met302Thr(p.M302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000303904
Start	100091110:100091110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607G>A
AA Mutation	p.Val203Ile(p.V203I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000303904
Start	100089391:100089391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.178T>C
AA Mutation	p.Ser60Pro(p.S60P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000303904
Start	100089392:100089392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.179C>T
AA Mutation	p.Ser60Phe(p.S60F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000303904
Start	100091252:100091252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664A>T
AA Mutation	p.Ile222Leu(p.I222L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303904
Start	100091088:100091088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377111966
CDS Mutation	c.585G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303904
Start	100091445:100091445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745924412
CDS Mutation	c.768C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303904
Start	100091251:100091251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303904
Start	100089032:100089032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> COPS6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303904
Start	100091267:100091267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679G>A
AA Mutation	p.Ala227Thr(p.A227T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303904
Start	100089650:100089650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.238A>C
AA Mutation	p.Asn80His(p.N80H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000303904
Start	100089619:100089620(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.209_211dupGGG
AA Mutation	p.Gly70dup(p.G70dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript