Colon Cancer: Gene >> FITM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267426
Start	24132693:24132693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.749T>C
AA Mutation	p.Val250Ala(p.V250A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267426
Start	24131724:24131724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201965049
CDS Mutation	c.161G>A
AA Mutation	p.Arg54His(p.R54H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267426
Start	24131610:24131610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375038109
CDS Mutation	c.47G>A
AA Mutation	p.Arg16Gln(p.R16Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000267426
Start	24132288:24132288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.344C>T
AA Mutation	p.Thr115Ile(p.T115I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267426
Start	24132814:24132814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FITM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267426
Start	24132570:24132570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.626C>T
AA Mutation	p.Ala209Val(p.A209V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript