Colon Cancer: Gene >> LEF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265165
Start	108078252:108078252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.976A>G
AA Mutation	p.Ser326Gly(p.S326G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265165
Start	108079549:108079549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.788T>C
AA Mutation	p.Ile263Thr(p.I263T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265165
Start	108078314:108078314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914C>T
AA Mutation	p.Ala305Val(p.A305V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265165
Start	108167727:108167727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769814612
CDS Mutation	c.41A>G
AA Mutation	p.Asp14Gly(p.D14G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265165
Start	108078324:108078324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.904C>T
AA Mutation	p.Pro302Ser(p.P302S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265165
Start	108078312:108078312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916T>C
AA Mutation	p.Phe306Leu(p.F306L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265165
Start	108078303:108078303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925T>C
AA Mutation	p.Tyr309His(p.Y309H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265165
Start	108163620:108163620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362A>G
AA Mutation	p.Asn121Ser(p.N121S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265165
Start	108078342:108078342(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.886delA
AA Mutation	p.Arg296AspfsTer8(p.R296Dfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LEF1

No Mutation Annotation!