Colon Cancer: Gene >> RPUSD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315616
Start	40574049:40574049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1426G>A
AA Mutation	p.Asp476Asn(p.D476N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315616
Start	40571619:40571619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146217445
CDS Mutation	c.622C>T
AA Mutation	p.Arg208Trp(p.R208W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315616
Start	40573926:40573926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1303C>A
AA Mutation	p.Leu435Met(p.L435M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315616
Start	40574173:40574173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1550T>A
AA Mutation	p.Phe517Tyr(p.F517Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315616
Start	40574029:40574029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1406A>G
AA Mutation	p.Glu469Gly(p.E469G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315616
Start	40573713:40573713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090C>T
AA Mutation	p.Pro364Ser(p.P364S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315616
Start	40574159:40574159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1536A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000315616
Start	40573590:40573590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967G>T
AA Mutation	p.Glu323Ter(p.E323*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RPUSD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315616
Start	40574130:40574130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532193389
CDS Mutation	c.1507C>T
AA Mutation	p.Arg503Trp(p.R503W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315616
Start	40574153:40574153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1530G>A
Mutation Classification	Silent
Feature Type	Transcript