Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FEZF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442488
Start	122304247:122304247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191C>A
AA Mutation	p.Ser64Tyr(p.S64Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442488
Start	122302888:122302888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.980G>T
AA Mutation	p.Arg327Ile(p.R327I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000442488
Start	122304380:122304380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.58G>T
AA Mutation	p.Gly20Cys(p.G20C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000442488
Start	122302316:122302316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1109A>C
AA Mutation	p.Lys370Thr(p.K370T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442488
Start	122303717:122303717(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.721delA
AA Mutation	p.Ile241SerfsTer35(p.I241Sfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442488
Start	122303852:122303852(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.586delA
AA Mutation	p.Thr196ArgfsTer3(p.T196Rfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442488
Start	122303871:122303872(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.566dupC
AA Mutation	p.Leu190PhefsTer14(p.L190Ffs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FEZF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442488
Start	122303737:122303737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701C>T
AA Mutation	p.Ala234Val(p.A234V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442488
Start	122302301:122302301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1124A>G
AA Mutation	p.Asn375Ser(p.N375S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000442488
Start	122303665:122303665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773A>C
AA Mutation	p.Lys258Thr(p.K258T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript