Colon Cancer: Gene >> FEZF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283268
Start	62371639:62371639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.881G>A
AA Mutation	p.Arg294His(p.R294H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283268
Start	62370221:62370221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242G>T
AA Mutation	p.Lys414Asn(p.K414N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000283268
Start	62372262:62372262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368222900
CDS Mutation	c.607G>A
AA Mutation	p.Ala203Thr(p.A203T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000283268
Start	62370210:62370210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1253C>T
AA Mutation	p.Thr418Met(p.T418M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000283268
Start	62372324:62372324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.545C>T
AA Mutation	p.Pro182Leu(p.P182L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000283268
Start	62372753:62372753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.116C>T
AA Mutation	p.Thr39Met(p.T39M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000283268
Start	62372201:62372201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374025354
CDS Mutation	c.668C>T
AA Mutation	p.Ala223Val(p.A223V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000283268
Start	62372684:62372684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.185A>T
AA Mutation	p.Lys62Ile(p.K62I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283268
Start	62370227:62370227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283268
Start	62372479:62372479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283268
Start	62371590:62371590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283268
Start	62371569:62371569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.951C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283268
Start	62370206:62370206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750078095
CDS Mutation	c.1257C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283268
Start	62371296:62371296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1041G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283268
Start	62371605:62371605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283268
Start	62370197:62370197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1266C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283268
Start	62370209:62370209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000283268
Start	62370118:62370119(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1344dupC
AA Mutation	p.Ser449LeufsTer7(p.S449Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FEZF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283268
Start	62371247:62371247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090G>A
AA Mutation	p.Glu364Lys(p.E364K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283268
Start	62370206:62370206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750078095
CDS Mutation	c.1257C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283268
Start	62371605:62371605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.915C>T
Mutation Classification	Silent
Feature Type	Transcript