Colon Cancer: Gene >> UBXN11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374221
Start	26284442:26284442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200278768
CDS Mutation	c.893T>C
AA Mutation	p.Leu298Pro(p.L298P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374221
Start	26285833:26285833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.764C>A
AA Mutation	p.Pro255His(p.P255H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374221
Start	26282915:26282915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371990639
CDS Mutation	c.1100G>A
AA Mutation	p.Arg367Gln(p.R367Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374221
Start	26282525:26282525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1337C>A
AA Mutation	p.Pro446His(p.P446H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374221
Start	26282883:26282883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1132T>G
AA Mutation	p.Leu378Val(p.L378V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374221
Start	26285907:26285907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369607205
CDS Mutation	c.690C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374221
Start	26285494:26285494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.822G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> UBXN11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374221
Start	26282545:26282545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1317G>T
AA Mutation	p.Glu439Asp(p.E439D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374221
Start	26282783:26282783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1158G>C
AA Mutation	p.Gln386His(p.Q386H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript