Colon Cancer: Gene >> GOPC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368498
Start	117566971:117566971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115242892
CDS Mutation	c.1141G>A
AA Mutation	p.Val381Ile(p.V381I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368498
Start	117563381:117563381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1262T>G
AA Mutation	p.Phe421Cys(p.F421C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368498
Start	117569575:117569575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074G>T
AA Mutation	p.Gln358His(p.Q358H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368498
Start	117569605:117569605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1044G>T
AA Mutation	p.Lys348Asn(p.K348N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368498
Start	117575219:117575219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.608C>T
AA Mutation	p.Ala203Val(p.A203V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368498
Start	117566972:117566972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749282315
CDS Mutation	c.1140C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368498
Start	117569668:117569668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149907550
CDS Mutation	c.981C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GOPC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368498
Start	117575259:117575259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752823444
CDS Mutation	c.568C>T
AA Mutation	p.Arg190Cys(p.R190C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368498
Start	117573522:117573522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761G>A
AA Mutation	p.Arg254Gln(p.R254Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368498
Start	117563317:117563317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146035577
CDS Mutation	c.1326G>A
Mutation Classification	Silent
Feature Type	Transcript