Colon Cancer: Gene >> KLF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377126
Start	70413099:70413099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265C>T
AA Mutation	p.Pro89Ser(p.P89S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377126
Start	70413098:70413098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.266C>T
AA Mutation	p.Pro89Leu(p.P89L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377126
Start	70388005:70388005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.506G>C
AA Mutation	p.Gly169Ala(p.G169A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377126
Start	70387893:70387893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764995654
CDS Mutation	c.618G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377126
Start	70413286:70413286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766581282
CDS Mutation	c.78G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377126
Start	70387798:70387798(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.713delA
AA Mutation	p.Lys238ArgfsTer32(p.K238Rfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KLF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377126
Start	70412897:70412897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467A>C
AA Mutation	p.Lys156Thr(p.K156T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377126
Start	70413337:70413337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript