Colon Cancer: Gene >> F7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375581
Start	113113903:113113903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373C>G
AA Mutation	p.Leu125Val(p.L125V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375581
Start	113113760:113113760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.300C>A
AA Mutation	p.Phe100Leu(p.F100L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375581
Start	113118697:113118697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750980786
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Trp(p.R364W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375581
Start	113110719:113110719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160G>A
AA Mutation	p.Val54Ile(p.V54I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375581
Start	113110764:113110764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.205C>T
AA Mutation	p.Arg69Trp(p.R69W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375581
Start	113117476:113117476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685C>A
AA Mutation	p.Leu229Met(p.L229M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375581
Start	113116836:113116836(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.647delG
AA Mutation	p.Gly216AlafsTer17(p.G216Afs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> F7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375581
Start	113117587:113117587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764807079
CDS Mutation	c.796G>A
AA Mutation	p.Ala266Thr(p.A266T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375581
Start	113110718:113110718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763156842
CDS Mutation	c.159C>T
Mutation Classification	Silent
Feature Type	Transcript