Colon Cancer: Gene >> CCNF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397066
Start	2449427:2449427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1364C>A
AA Mutation	p.Ala455Glu(p.A455E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397066
Start	2453283:2453283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374120930
CDS Mutation	c.1561C>T
AA Mutation	p.Arg521Cys(p.R521C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397066
Start	2439443:2439443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753372697
CDS Mutation	c.685G>A
AA Mutation	p.Asp229Asn(p.D229N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397066
Start	2456577:2456577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373872375
CDS Mutation	c.1918G>A
AA Mutation	p.Val640Met(p.V640M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397066
Start	2438100:2438100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571G>A
AA Mutation	p.Gly191Ser(p.G191S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397066
Start	2456926:2456926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370448527
CDS Mutation	c.2267C>T
AA Mutation	p.Pro756Leu(p.P756L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397066
Start	2445546:2445546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1018C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397066
Start	2448891:2448891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371121254
CDS Mutation	c.1131C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397066
Start	2443717:2443717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201813739
CDS Mutation	c.846C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397066
Start	2453472:2453472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs553385838
CDS Mutation	c.1650G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000397066
Start	2432970:2432970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181C>T
AA Mutation	p.Gln61Ter(p.Q61*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000397066
Start	2439368:2439368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610C>T
AA Mutation	p.Gln204Ter(p.Q204*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CCNF

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397066
Start	2449452:2449452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200891175
CDS Mutation	c.1389G>A
Mutation Classification	Silent
Feature Type	Transcript