Colon Cancer: Gene >> FEN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305885
Start	61795421:61795421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.60G>T
AA Mutation	p.Glu20Asp(p.E20D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305885
Start	61795968:61795968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607C>T
AA Mutation	p.Pro203Ser(p.P203S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305885
Start	61796094:61796094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.733C>G
AA Mutation	p.Arg245Gly(p.R245G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305885
Start	61796370:61796370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1009C>A
AA Mutation	p.Gln337Lys(p.Q337K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305885
Start	61796377:61796377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573495657
CDS Mutation	c.1016G>A
AA Mutation	p.Arg339His(p.R339H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305885
Start	61795718:61795718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745612425
CDS Mutation	c.357C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305885
Start	61795646:61795646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371846488
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FEN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305885
Start	61796347:61796347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.986G>A
AA Mutation	p.Ser329Asn(p.S329N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript