Colon Cancer: Gene >> PRSS37

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350549
Start	141839363:141839363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151C>A
AA Mutation	p.Leu51Met(p.L51M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350549
Start	141836460:141836460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745313899
CDS Mutation	c.643G>A
AA Mutation	p.Val215Ile(p.V215I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350549
Start	141838068:141838068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222C>A
AA Mutation	p.Asp74Glu(p.D74E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350549
Start	141836457:141836457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756834067
CDS Mutation	c.646G>A
AA Mutation	p.Gly216Ser(p.G216S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350549
Start	141836496:141836496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773596053
CDS Mutation	c.607C>A
AA Mutation	p.Gln203Lys(p.Q203K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350549
Start	141837163:141837163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516C>A
AA Mutation	p.His172Gln(p.H172Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000350549
Start	141837132:141837132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547G>C
AA Mutation	p.Val183Leu(p.V183L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350549
Start	141837930:141837930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189550606
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350549
Start	141836461:141836461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146774956
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350549
Start	141838035:141838035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149011966
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PRSS37

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350549
Start	141838068:141838068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200503952
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript