Colon Cancer: Gene >> GPC5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377067
Start	91728551:91728551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372530892
CDS Mutation	c.1040G>A
AA Mutation	p.Arg347His(p.R347H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377067
Start	92866387:92866387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1667C>A
AA Mutation	p.Ser556Tyr(p.S556Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377067
Start	91728647:91728647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138581416
CDS Mutation	c.1136C>T
AA Mutation	p.Thr379Met(p.T379M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377067
Start	91693405:91693405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>A
AA Mutation	p.Gly182Ser(p.G182S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377067
Start	91448902:91448902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772585092
CDS Mutation	c.305G>A
AA Mutation	p.Arg102Gln(p.R102Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377067
Start	91399203:91399203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157C>T
AA Mutation	p.Arg53Trp(p.R53W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377067
Start	91693634:91693634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773G>T
AA Mutation	p.Cys258Phe(p.C258F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377067
Start	91693529:91693529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201373834
CDS Mutation	c.668G>A
AA Mutation	p.Arg223His(p.R223H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377067
Start	91693248:91693248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.387C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377067
Start	91693521:91693521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.660G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377067
Start	91693230:91693230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.369T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377067
Start	92866310:92866310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1590T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377067
Start	91693356:91693357(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.501dupT
AA Mutation	p.Asp168Ter(p.D168*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000377067
Start	91756422:91756422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1280+2T>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GPC5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377067
Start	91728580:91728580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772838827
CDS Mutation	c.1069C>T
AA Mutation	p.Arg357Cys(p.R357C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377067
Start	91756331:91756331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1191C>A
AA Mutation	p.Phe397Leu(p.F397L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript