Colon Cancer: Gene >> GPI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356487
Start	34366816:34366816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247C>T
AA Mutation	p.Arg83Trp(p.R83W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356487
Start	34393260:34393260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748408705
CDS Mutation	c.817C>T
AA Mutation	p.Arg273Cys(p.R273C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356487
Start	34396615:34396615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774225651
CDS Mutation	c.1227G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356487
Start	34366797:34366797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150838903
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356487
Start	34399976:34399976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766494581
CDS Mutation	c.1617C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356487
Start	34393304:34393304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371025511
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356487
Start	34365311:34365311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572523544
CDS Mutation	c.45A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356487
Start	34399293:34399293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34604585
CDS Mutation	c.1356G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356487
Start	34366369:34366369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.147G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356487
Start	34394054:34394054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780075559
CDS Mutation	c.1050G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356487
Start	34396377:34396377(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1144delG
AA Mutation	p.Glu382SerfsTer20(p.E382Sfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GPI

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356487
Start	34366826:34366826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370578920
CDS Mutation	c.257A>G
AA Mutation	p.Asn86Ser(p.N86S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356487
Start	34399977:34399977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547475819
CDS Mutation	c.1618G>A
AA Mutation	p.Ala540Thr(p.A540T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356487
Start	34399741:34399741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138799755
CDS Mutation	c.1497C>T
Mutation Classification	Silent
Feature Type	Transcript