Colon Cancer: Gene >> PCDHGC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308177
Start	141477401:141477401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1285G>A
AA Mutation	p.Ala429Thr(p.A429T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308177
Start	141477446:141477446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330C>T
AA Mutation	p.Arg444Cys(p.R444C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308177
Start	141476987:141476987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871G>A
AA Mutation	p.Val291Met(p.V291M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308177
Start	141478496:141478496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2380C>T
AA Mutation	p.Pro794Ser(p.P794S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308177
Start	141477504:141477504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1388A>G
AA Mutation	p.Asp463Gly(p.D463G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308177
Start	141476659:141476659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.543G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308177
Start	141477100:141477100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308177
Start	141476716:141476716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308177
Start	141476383:141476383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308177
Start	141476902:141476902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308177
Start	141478175:141478175(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2066delA
AA Mutation	p.Asn689IlefsTer10(p.N689Ifs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308177
Start	141477782:141477782(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1668delT
AA Mutation	p.Phe556LeufsTer34(p.F556Lfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PCDHGC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308177
Start	141476340:141476340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224G>T
AA Mutation	p.Arg75Ile(p.R75I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308177
Start	141477489:141477489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1373C>A
AA Mutation	p.Ser458Tyr(p.S458Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308177
Start	141478498:141478498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2382G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308177
Start	141478531:141478531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2415C>T
Mutation Classification	Silent
Feature Type	Transcript