Colon Cancer: Gene >> KLF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374672
Start	107485870:107485870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321G>A
AA Mutation	p.Asp441Asn(p.D441N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374672
Start	107485905:107485905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286A>T
AA Mutation	p.Asp429Val(p.D429V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374672
Start	107489018:107489018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.38G>A
AA Mutation	p.Ser13Asn(p.S13N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374672
Start	107488203:107488203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191A>T
AA Mutation	p.Asp64Val(p.D64V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374672
Start	107487046:107487046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246C>T
AA Mutation	p.His416Tyr(p.H416Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374672
Start	107488024:107488024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751611404
CDS Mutation	c.370G>A
AA Mutation	p.Val124Met(p.V124M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374672
Start	107488009:107488009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.385T>C
AA Mutation	p.Ser129Pro(p.S129P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374672
Start	107487551:107487551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.843G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374672
Start	107485905:107485906(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1285_1286delGA
AA Mutation	p.Asp429LeufsTer13(p.D429Lfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KLF4

No Mutation Annotation!