Colon Cancer: Gene >> FNDC5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373471
Start	32868222:32868222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369474610
CDS Mutation	c.377G>A
AA Mutation	p.Arg126His(p.R126H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373471
Start	32867777:32867777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189231805
CDS Mutation	c.475G>A
AA Mutation	p.Val159Ile(p.V159I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373471
Start	32868220:32868220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.379G>C
AA Mutation	p.Glu127Gln(p.E127Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373471
Start	32868222:32868222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.377G>C
AA Mutation	p.Arg126Pro(p.R126P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373471
Start	32867792:32867792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460G>A
AA Mutation	p.Glu154Lys(p.E154K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373471
Start	32867755:32867755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773770710
CDS Mutation	c.497C>T
AA Mutation	p.Ala166Val(p.A166V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FNDC5

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373471
Start	32868203:32868203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.396C>A
Mutation Classification	Silent
Feature Type	Transcript