Colon Cancer: Gene >> CPA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130367537:130367537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1004G>A
AA Mutation	p.Arg335Gln(p.R335Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130359620:130359620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782749167
CDS Mutation	c.365C>T
AA Mutation	p.Ala122Val(p.A122V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130347834:130347834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.185T>C
AA Mutation	p.Leu62Pro(p.L62P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130347837:130347837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188A>C
AA Mutation	p.Lys63Thr(p.K63T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130361236:130361236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526G>C
AA Mutation	p.Val176Leu(p.V176L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130363485:130363485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.814A>G
AA Mutation	p.Arg272Gly(p.R272G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130362484:130362484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.581G>T
AA Mutation	p.Gly194Val(p.G194V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130361215:130361215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505T>C
AA Mutation	p.Phe169Leu(p.F169L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130346538:130346538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.53G>C
AA Mutation	p.Arg18Thr(p.R18T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130367960:130367960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093T>C
AA Mutation	p.Tyr365His(p.Y365H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393213
Start	130363472:130363472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.801C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393213
Start	130367956:130367956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1089C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393213
Start	130368483:130368483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1197G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393213
Start	130368434:130368435(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1149dupC
AA Mutation	p.Trp384LeufsTer4(p.W384Lfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CPA5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130346507:130346507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200717171
CDS Mutation	c.22G>A
AA Mutation	p.Gly8Arg(p.G8R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130347801:130347801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.152A>C
AA Mutation	p.Lys51Thr(p.K51T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393213
Start	130361182:130361182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782787226
CDS Mutation	c.472G>A
AA Mutation	p.Asp158Asn(p.D158N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript