Colon Cancer: Gene >> POLB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265421
Start	42344964:42344964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.131C>T
AA Mutation	p.Ser44Phe(p.S44F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265421
Start	42371647:42371647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766919977
CDS Mutation	c.998G>A
AA Mutation	p.Arg333Gln(p.R333Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265421
Start	42361318:42361318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.574G>C
AA Mutation	p.Asp192His(p.D192H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265421
Start	42369927:42369927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.852T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265421
Start	42371596:42371596(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs780460727
CDS Mutation	c.951delA
AA Mutation	p.Asp318ThrfsTer42(p.D318Tfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> POLB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265421
Start	42338678:42338678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54G>A
AA Mutation	p.Met18Ile(p.M18I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265421
Start	42357200:42357200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Cys(p.R152C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000265421
Start	42371574:42371574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925G>T
AA Mutation	p.Glu309Ter(p.E309*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript