Colon Cancer: Gene >> CPA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000011292
Start	130383741:130383741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643A>G
AA Mutation	p.Ile215Val(p.I215V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000011292
Start	130383741:130383741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643A>C
AA Mutation	p.Ile215Leu(p.I215L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000011292
Start	130381766:130381766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375929600
CDS Mutation	c.284C>T
AA Mutation	p.Ser95Leu(p.S95L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000011292
Start	130385288:130385288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.930G>T
AA Mutation	p.Gln310His(p.Q310H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000011292
Start	130381112:130381112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547564304
CDS Mutation	c.80G>A
AA Mutation	p.Arg27Gln(p.R27Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000011292
Start	130385205:130385205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782561684
CDS Mutation	c.847G>A
AA Mutation	p.Glu283Lys(p.E283K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000011292
Start	130385314:130385314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956A>C
AA Mutation	p.Lys319Thr(p.K319T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011292
Start	130381824:130381824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.342C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011292
Start	130384613:130384613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368689434
CDS Mutation	c.774C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011292
Start	130383785:130383785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370302338
CDS Mutation	c.687G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011292
Start	130383429:130383429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.522C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011292
Start	130382146:130382146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011292
Start	130385186:130385186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781912694
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000011292
Start	130381102:130381102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.70C>T
AA Mutation	p.Gln24Ter(p.Q24*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000011292
Start	130381678:130381678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371401173
CDS Mutation	c.196C>T
AA Mutation	p.Arg66Ter(p.R66*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CPA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000011292
Start	130381811:130381811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537076438
CDS Mutation	c.329G>A
AA Mutation	p.Arg110Gln(p.R110Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000011292
Start	130381112:130381112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547564304
CDS Mutation	c.80G>A
AA Mutation	p.Arg27Gln(p.R27Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000011292
Start	130385886:130385886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1035G>A
Mutation Classification	Silent
Feature Type	Transcript