Colon Cancer: Gene >> TALDO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319006
Start	764308:764308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856A>C
AA Mutation	p.Lys286Gln(p.K286Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319006
Start	760142:760142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764703431
CDS Mutation	c.350C>T
AA Mutation	p.Ala117Val(p.A117V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319006
Start	763367:763367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.485T>C
AA Mutation	p.Ile162Thr(p.I162T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319006
Start	763825:763825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773023043
CDS Mutation	c.716G>A
AA Mutation	p.Arg239His(p.R239H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319006
Start	763381:763381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499A>G
AA Mutation	p.Thr167Ala(p.T167A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319006
Start	763910:763910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142263629
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TALDO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319006
Start	759027:759027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778205812
CDS Mutation	c.299C>T
AA Mutation	p.Pro100Leu(p.P100L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript