Colon Cancer: Gene >> UPK1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222275
Start	35675952:35675952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377645091
CDS Mutation	c.581C>T
AA Mutation	p.Thr194Met(p.T194M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222275
Start	35677842:35677842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679G>A
AA Mutation	p.Asp227Asn(p.D227N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222275
Start	35668634:35668634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151183070
CDS Mutation	c.265C>T
AA Mutation	p.Arg89Cys(p.R89C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000222275
Start	35668653:35668653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61744570
CDS Mutation	c.284C>T
AA Mutation	p.Thr95Met(p.T95M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222275
Start	35668549:35668549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222275
Start	35668633:35668633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222275
Start	35666818:35666818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772358911
CDS Mutation	c.6G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> UPK1A

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222275
Start	35673521:35673521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760111506
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript