Colon Cancer: Gene >> KLF7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309446
Start	207081236:207081236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.886C>T
AA Mutation	p.Leu296Phe(p.L296F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309446
Start	207165528:207165528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.41A>G
AA Mutation	p.Gln14Arg(p.Q14R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309446
Start	207088539:207088539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.776G>A
AA Mutation	p.Arg259His(p.R259H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309446
Start	207123828:207123828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371003779
CDS Mutation	c.679C>T
AA Mutation	p.Arg227Trp(p.R227W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309446
Start	207165521:207165521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.48C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309446
Start	207124038:207124039(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.467_468dupCT
AA Mutation	p.Ala157LeufsTer7(p.A157Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> KLF7

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309446
Start	207123835:207123835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201005804
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript