Colon Cancer: Gene >> POLE2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000216367
Start	49664673:49664673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635A>G
AA Mutation	p.Gln212Arg(p.Q212R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216367
Start	49651321:49651321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1268T>C
AA Mutation	p.Met423Thr(p.M423T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216367
Start	49688157:49688157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47T>C
AA Mutation	p.Leu16Ser(p.L16S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216367
Start	49651355:49651355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234A>C
AA Mutation	p.Ile412Leu(p.I412L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216367
Start	49655012:49655012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1011T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216367
Start	49651308:49651308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760488544
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216367
Start	49669593:49669593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.423C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216367
Start	49666390:49666390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216367
Start	49650391:49650392(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1370_1371delAT
AA Mutation	p.Tyr457CysfsTer9(p.Y457Cfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> POLE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216367
Start	49654063:49654063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138C>T
AA Mutation	p.Pro380Ser(p.P380S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216367
Start	49650295:49650295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374026236
CDS Mutation	c.1467G>A
Mutation Classification	Silent
Feature Type	Transcript