Colon Cancer: Gene >> SEPHS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327347
Start	13333827:13333827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.550G>A
AA Mutation	p.Glu184Lys(p.E184K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327347
Start	13319209:13319209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1112G>A
AA Mutation	p.Arg371Gln(p.R371Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327347
Start	13319236:13319236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1085G>A
AA Mutation	p.Arg362His(p.R362H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327347
Start	13344862:13344862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89G>A
AA Mutation	p.Gly30Asp(p.G30D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327347
Start	13338781:13338781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221C>A
AA Mutation	p.Pro74His(p.P74H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327347
Start	13322846:13322846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.953C>T
AA Mutation	p.Pro318Leu(p.P318L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327347
Start	13322851:13322851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327347
Start	13338771:13338771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567954830
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327347
Start	13322881:13322881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564065082
CDS Mutation	c.918C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327347
Start	13344894:13344894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.57G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SEPHS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327347
Start	13344833:13344833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.118A>G
AA Mutation	p.Lys40Glu(p.K40E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript