Colon Cancer: Gene >> GP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000417454
Start	55027778:55027778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773642386
CDS Mutation	c.410G>A
AA Mutation	p.Arg137Gln(p.R137Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000417454
Start	55027776:55027776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412T>C
AA Mutation	p.Tyr138His(p.Y138H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000417454
Start	55032325:55032325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756588702
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Trp(p.R47W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000417454
Start	55027671:55027671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517G>A
AA Mutation	p.Ala173Thr(p.A173T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000417454
Start	55032204:55032204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759426349
CDS Mutation	c.260G>A
AA Mutation	p.Arg87His(p.R87H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000417454
Start	55027652:55027652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751979972
CDS Mutation	c.536G>A
AA Mutation	p.Arg179Gln(p.R179Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000417454
Start	55032141:55032141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323C>T
AA Mutation	p.Thr108Met(p.T108M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000417454
Start	55015138:55015138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803G>A
AA Mutation	p.Gly268Asp(p.G268D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000417454
Start	55015732:55015732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.726G>T
AA Mutation	p.Glu242Asp(p.E242D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript