Colon Cancer: Gene >> KLF10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285407
Start	102650227:102650227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757650416
CDS Mutation	c.1348C>T
AA Mutation	p.Arg450Cys(p.R450C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285407
Start	102651863:102651863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469C>T
AA Mutation	p.Arg157Cys(p.R157C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285407
Start	102650385:102650385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1190A>C
AA Mutation	p.Lys397Thr(p.K397T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285407
Start	102650278:102650278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1297A>G
AA Mutation	p.Met433Val(p.M433V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285407
Start	102651256:102651256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1076C>T
AA Mutation	p.Pro359Leu(p.P359L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KLF10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285407
Start	102651319:102651319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777838088
CDS Mutation	c.1013G>A
AA Mutation	p.Gly338Asp(p.G338D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285407
Start	102651327:102651327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745774507
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript