Colon Cancer: Gene >> SAE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000270225
Start	47169879:47169879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689A>T
AA Mutation	p.Lys230Met(p.K230M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000270225
Start	47152972:47152972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.459C>A
AA Mutation	p.Phe153Leu(p.F153L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000270225
Start	47143522:47143522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199801330
CDS Mutation	c.127G>A
AA Mutation	p.Gly43Ser(p.G43S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000270225
Start	47150349:47150349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>A
AA Mutation	p.Glu120Lys(p.E120K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000270225
Start	47152958:47152958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445A>T
AA Mutation	p.Asn149Tyr(p.N149Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000270225
Start	47197268:47197268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769C>T
AA Mutation	p.Pro257Ser(p.P257S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270225
Start	47209162:47209162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.952C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270225
Start	47155159:47155159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.573G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000270225
Start	47155162:47155162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SAE1

No Mutation Annotation!