Colon Cancer: Gene >> CLUAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000576634
Start	3504749:3504749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770554988
CDS Mutation	c.52T>C
AA Mutation	p.Tyr18His(p.Y18H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000576634
Start	3519987:3519987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664T>G
AA Mutation	p.Leu222Val(p.L222V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000576634
Start	3508347:3508347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531380218
CDS Mutation	c.278C>T
AA Mutation	p.Ala93Val(p.A93V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000576634
Start	3506362:3506362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749597681
CDS Mutation	c.166G>A
AA Mutation	p.Val56Met(p.V56M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000576634
Start	3504795:3504795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98G>A
AA Mutation	p.Gly33Glu(p.G33E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000576634
Start	3501077:3501077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10C>T
AA Mutation	p.Arg4Cys(p.R4C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000576634
Start	3536166:3536166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377189683
CDS Mutation	c.1137C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000576634
Start	3504746:3504746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49G>T
AA Mutation	p.Gly17Ter(p.G17*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	start_lost
Transcription ID	ENST00000576634
Start	3501069:3501069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CLUAP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000576634
Start	3506343:3506343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.147G>T
AA Mutation	p.Gln49His(p.Q49H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000576634
Start	3519974:3519974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748456720
CDS Mutation	c.651C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000576634
Start	3519932:3519932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609C>A
Mutation Classification	Silent
Feature Type	Transcript