Colon Cancer: Gene >> TOM1L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000575882
Start	54930092:54930092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748448745
CDS Mutation	c.740G>A
AA Mutation	p.Arg247Gln(p.R247Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000575882
Start	54912729:54912729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286T>A
AA Mutation	p.Phe96Ile(p.F96I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000575882
Start	54912809:54912809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.366C>A
AA Mutation	p.Phe122Leu(p.F122L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000575882
Start	54913786:54913786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773984383
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000575882
Start	54900887:54900887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000575882
Start	54912684:54912684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568678217
CDS Mutation	c.241C>T
AA Mutation	p.Gln81Ter(p.Q81*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000575882
Start	54915791:54915791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771053348
CDS Mutation	c.649C>T
AA Mutation	p.Arg217Ter(p.R217*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TOM1L1

No Mutation Annotation!