Colon Cancer: Gene >> GPC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264039
Start	240465104:240465104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750226747
CDS Mutation	c.1162G>A
AA Mutation	p.Asp388Asn(p.D388N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264039
Start	240464711:240464711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751991629
CDS Mutation	c.979G>A
AA Mutation	p.Ala327Thr(p.A327T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264039
Start	240459055:240459055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192G>T
AA Mutation	p.Gln64His(p.Q64H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264039
Start	240465504:240465504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1300G>A
AA Mutation	p.Ala434Thr(p.A434T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264039
Start	240462317:240462317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452A>G
AA Mutation	p.Tyr151Cys(p.Y151C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264039
Start	240463393:240463393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764A>G
AA Mutation	p.Tyr255Cys(p.Y255C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264039
Start	240465645:240465645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775242022
CDS Mutation	c.1441G>A
AA Mutation	p.Ala481Thr(p.A481T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264039
Start	240462558:240462558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754067522
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264039
Start	240464698:240464698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201081083
CDS Mutation	c.966G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000264039
Start	240463346:240463346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.718-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GPC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264039
Start	240466132:240466132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1519A>C
AA Mutation	p.Ser507Arg(p.S507R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript