Colon Cancer: Gene >> SEPT9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000427177
Start	77402068:77402068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86G>T
AA Mutation	p.Arg29Ile(p.R29I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000427177
Start	77402452:77402452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470C>T
AA Mutation	p.Pro157Leu(p.P157L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000427177
Start	77402269:77402269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287C>T
AA Mutation	p.Ser96Leu(p.S96L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000427177
Start	77487513:77487513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1003C>T
AA Mutation	p.Arg335Cys(p.R335C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000427177
Start	77490816:77490816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760752419
CDS Mutation	c.1337C>T
AA Mutation	p.Ala446Val(p.A446V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000427177
Start	77488797:77488797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1195C>T
AA Mutation	p.Arg399Cys(p.R399C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427177
Start	77402396:77402396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000427177
Start	77402114:77402114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.132C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000427177
Start	77488730:77488730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1128G>A
AA Mutation	p.Trp376Ter(p.W376*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SEPT9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000427177
Start	77498608:77498608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773416606
CDS Mutation	c.1711G>A
AA Mutation	p.Ala571Thr(p.A571T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript