Colon Cancer: Gene >> SCPEP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262288
Start	56998451:56998451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.947C>T
AA Mutation	p.Pro316Leu(p.P316L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262288
Start	56978232:56978232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73G>A
AA Mutation	p.Ala25Thr(p.A25T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262288
Start	57002086:57002086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377343195
CDS Mutation	c.1201G>A
AA Mutation	p.Ala401Thr(p.A401T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262288
Start	57002035:57002035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771883135
CDS Mutation	c.1150C>T
AA Mutation	p.Arg384Trp(p.R384W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262288
Start	57002158:57002158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1273T>C
AA Mutation	p.Trp425Arg(p.W425R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262288
Start	57002059:57002059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769859901
CDS Mutation	c.1174C>T
AA Mutation	p.Pro392Ser(p.P392S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262288
Start	56978214:56978214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.55C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262288
Start	57002103:57002103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1218T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262288
Start	56997012:56997012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148083534
CDS Mutation	c.837G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000262288
Start	56995621:56995622(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.772_773insGACCCACTT
AA Mutation	p.Met258delinsArgProThrLeu(p.M258delinsRPTL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SCPEP1

No Mutation Annotation!