Colon Cancer: Gene >> PREP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105353016:105353016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774687832
CDS Mutation	c.779G>A
AA Mutation	p.Arg260Gln(p.R260Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105328873:105328873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1169A>C
AA Mutation	p.Lys390Thr(p.K390T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105323727:105323727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255C>T
AA Mutation	p.Pro419Ser(p.P419S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105278292:105278292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774977355
CDS Mutation	c.1985G>A
AA Mutation	p.Arg662His(p.R662H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105278334:105278334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1943A>G
AA Mutation	p.His648Arg(p.H648R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105278293:105278293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758277302
CDS Mutation	c.1984C>T
AA Mutation	p.Arg662Cys(p.R662C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105285497:105285497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765121838
CDS Mutation	c.1538C>T
AA Mutation	p.Thr513Met(p.T513M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105285510:105285510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1525G>A
AA Mutation	p.Glu509Lys(p.E509K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105368979:105368979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.641T>C
AA Mutation	p.Val214Ala(p.V214A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105278247:105278247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2030A>T
AA Mutation	p.Lys677Met(p.K677M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105377439:105377439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201G>A
AA Mutation	p.Met67Ile(p.M67I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369110
Start	105376231:105376231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.279T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369110
Start	105278237:105278237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116581811
CDS Mutation	c.2040C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369110
Start	105281811:105281811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141753924
CDS Mutation	c.1773C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369110
Start	105285496:105285496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372854817
CDS Mutation	c.1539G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369110
Start	105397871:105397871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186413675
CDS Mutation	c.102C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369110
Start	105278269:105278269(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2008delC
AA Mutation	p.Leu670CysfsTer20(p.L670Cfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369110
Start	105288837:105288838(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1374dupA
AA Mutation	p.Gly459ArgfsTer58(p.G459Rfs*58)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PREP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105285497:105285497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765121838
CDS Mutation	c.1538C>T
AA Mutation	p.Thr513Met(p.T513M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369110
Start	105288872:105288872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1340G>A
AA Mutation	p.Gly447Asp(p.G447D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369110
Start	105333417:105333417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.912G>A
Mutation Classification	Silent
Feature Type	Transcript