Colon Cancer: Gene >> CSPG5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383738
Start	47562656:47562656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1645G>A
AA Mutation	p.Gly549Ser(p.G549S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383738
Start	47577191:47577191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.835G>A
AA Mutation	p.Glu279Lys(p.E279K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000383738
Start	47577761:47577761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265C>A
AA Mutation	p.Leu89Met(p.L89M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000383738
Start	47576872:47576872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154G>A
AA Mutation	p.Gly385Asp(p.G385D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000383738
Start	47577359:47577359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.667G>A
AA Mutation	p.Ala223Thr(p.A223T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000383738
Start	47572873:47572873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1195T>C
AA Mutation	p.Cys399Arg(p.C399R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000383738
Start	47572785:47572785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775179910
CDS Mutation	c.1283C>T
AA Mutation	p.Ser428Leu(p.S428L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383738
Start	47577417:47577417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199702237
CDS Mutation	c.609G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383738
Start	47577015:47577015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373067610
CDS Mutation	c.1011C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383738
Start	47577360:47577360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383738
Start	47572799:47572799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1269C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383738
Start	47577396:47577396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CSPG5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383738
Start	47572695:47572695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759474596
CDS Mutation	c.1373G>A
AA Mutation	p.Arg458His(p.R458H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383738
Start	47572842:47572842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1226G>A
AA Mutation	p.Gly409Glu(p.G409E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000383738
Start	47572713:47572713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201603317
CDS Mutation	c.1355C>T
AA Mutation	p.Thr452Met(p.T452M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383738
Start	47562735:47562735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752259042
CDS Mutation	c.1566C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383738
Start	47577387:47577387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746592573
CDS Mutation	c.639C>T
Mutation Classification	Silent
Feature Type	Transcript