Colon Cancer: Gene >> FEZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278919
Start	125456079:125456079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.695T>C
AA Mutation	p.Leu232Pro(p.L232P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278919
Start	125456019:125456019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755A>T
AA Mutation	p.Gln252Leu(p.Q252L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278919
Start	125456049:125456049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.725C>A
AA Mutation	p.Ala242Asp(p.A242D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278919
Start	125448522:125448522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142T>C
AA Mutation	p.Leu381Pro(p.L381P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278919
Start	125448517:125448517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1147G>A
AA Mutation	p.Asp383Asn(p.D383N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000278919
Start	125460655:125460655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510G>T
AA Mutation	p.Glu170Asp(p.E170D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000278919
Start	125460510:125460510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745432120
CDS Mutation	c.655T>C
AA Mutation	p.Trp219Arg(p.W219R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FEZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278919
Start	125481616:125481616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329C>G
AA Mutation	p.Thr110Arg(p.T110R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278919
Start	125489645:125489645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.133G>A
AA Mutation	p.Glu45Lys(p.E45K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278919
Start	125481610:125481610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.335A>G
AA Mutation	p.Asn112Ser(p.N112S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278919
Start	125489624:125489624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.154G>A
AA Mutation	p.Glu52Lys(p.E52K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278919
Start	125456075:125456075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755860059
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript