Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PRSS55

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328655
Start	10538588:10538588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.854A>G
AA Mutation	p.Tyr285Cys(p.Y285C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328655
Start	10532927:10532927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202134590
CDS Mutation	c.620C>T
AA Mutation	p.Thr207Met(p.T207M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328655
Start	10538650:10538650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916T>C
AA Mutation	p.Phe306Leu(p.F306L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328655
Start	10531330:10531330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.383A>G
AA Mutation	p.Asp128Gly(p.D128G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000328655
Start	10538716:10538716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.982C>A
AA Mutation	p.Pro328Thr(p.P328T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328655
Start	10538619:10538619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.885C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328655
Start	10529634:10529634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746250450
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328655
Start	10531451:10531451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560455180
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PRSS55

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328655
Start	10529522:10529522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.170C>A
AA Mutation	p.Ser57Tyr(p.S57Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328655
Start	10529573:10529573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144558050
CDS Mutation	c.221C>T
AA Mutation	p.Ala74Val(p.A74V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328655
Start	10538611:10538611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877C>A
AA Mutation	p.Leu293Ile(p.L293I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328655
Start	10538675:10538675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.941C>A
AA Mutation	p.Ser314Tyr(p.S314Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328655
Start	10529688:10529688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750765458
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328655
Start	10538499:10538499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765C>A
Mutation Classification	Silent
Feature Type	Transcript