Colon Cancer: Gene >> PORCN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326194
Start	48512422:48512422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.470G>A
AA Mutation	p.Gly157Asp(p.G157D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326194
Start	48512679:48512679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.646C>A
AA Mutation	p.Pro216Thr(p.P216T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000326194
Start	48511322:48511322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.164G>A
AA Mutation	p.Ser55Asn(p.S55N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000326194
Start	48512395:48512395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782273836
CDS Mutation	c.443C>T
AA Mutation	p.Thr148Met(p.T148M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000326194
Start	48512448:48512448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496G>A
AA Mutation	p.Val166Ile(p.V166I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326194
Start	48514255:48514255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326194
Start	48514570:48514570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.891A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326194
Start	48514321:48514321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376623776
CDS Mutation	c.801G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326194
Start	48512699:48512699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782299289
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000326194
Start	48512690:48512690(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.661delC
AA Mutation	p.Leu221SerfsTer19(p.L221Sfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000326194
Start	48517182:48517182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1174-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> PORCN

No Mutation Annotation!