Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CPA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297770
Start	67511639:67511639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.334C>A
AA Mutation	p.Leu112Ile(p.L112I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000297770
Start	67517986:67517986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756306763
CDS Mutation	c.254A>G
AA Mutation	p.His85Arg(p.H85R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000297770
Start	67746036:67746036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94C>T
AA Mutation	p.Leu32Phe(p.L32F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000297770
Start	67509564:67509564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.487T>C
AA Mutation	p.Phe163Leu(p.F163L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297770
Start	67422633:67422633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1185T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297770
Start	67746049:67746049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369835154
CDS Mutation	c.81G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CPA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000297770
Start	67746061:67746061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.69G>T
AA Mutation	p.Lys23Asn(p.K23N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297770
Start	67422627:67422627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760234221
CDS Mutation	c.1191C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000297770
Start	67434134:67434134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.945G>A
Mutation Classification	Silent
Feature Type	Transcript