Colon Cancer: Gene >> VCP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358901
Start	35066695:35066695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.425C>T
AA Mutation	p.Ala142Val(p.A142V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358901
Start	35062234:35062234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928G>A
AA Mutation	p.Ala310Thr(p.A310T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358901
Start	35062008:35062008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1076G>A
AA Mutation	p.Arg359Gln(p.R359Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358901
Start	35062029:35062029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747902669
CDS Mutation	c.1055G>A
AA Mutation	p.Ser352Asn(p.S352N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358901
Start	35059638:35059638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1859T>C
AA Mutation	p.Ile620Thr(p.I620T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358901
Start	35059584:35059584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1913G>A
AA Mutation	p.Arg638His(p.R638H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358901
Start	35057457:35057457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2234G>A
AA Mutation	p.Arg745His(p.R745H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358901
Start	35060501:35060501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1507T>G
AA Mutation	p.Phe503Val(p.F503V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000358901
Start	35061103:35061103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1271G>A
AA Mutation	p.Arg424His(p.R424H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358901
Start	35062247:35062247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.915G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358901
Start	35066790:35066790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358901
Start	35057432:35057432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2259G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VCP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358901
Start	35059167:35059167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2057A>G
AA Mutation	p.Asp686Gly(p.D686G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358901
Start	35065254:35065254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.573A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358901
Start	35066727:35066727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760755090
CDS Mutation	c.393C>T
Mutation Classification	Silent
Feature Type	Transcript