Colon Cancer: Gene >> UBA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333486
Start	49812000:49812000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809C>T
AA Mutation	p.Ala270Val(p.A270V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333486
Start	49813066:49813066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140891266
CDS Mutation	c.463G>A
AA Mutation	p.Val155Met(p.V155M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333486
Start	49810768:49810768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772891199
CDS Mutation	c.1295G>A
AA Mutation	p.Arg432His(p.R432H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000333486
Start	49805361:49805361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2986T>C
AA Mutation	p.Cys996Arg(p.C996R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000333486
Start	49805960:49805960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2846G>A
AA Mutation	p.Gly949Asp(p.G949D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000333486
Start	49808433:49808433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2383G>A
AA Mutation	p.Glu795Lys(p.E795K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000333486
Start	49808993:49808993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776826132
CDS Mutation	c.2330C>T
AA Mutation	p.Ser777Leu(p.S777L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333486
Start	49813088:49813088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.441G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333486
Start	49808104:49808104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2439C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000333486
Start	49809541:49809541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2088+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> UBA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333486
Start	49811306:49811306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1089G>A
AA Mutation	p.Met363Ile(p.M363I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333486
Start	49812488:49812488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.614A>G
AA Mutation	p.Asp205Gly(p.D205G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333486
Start	49810013:49810013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757115951
CDS Mutation	c.1804C>T
AA Mutation	p.Arg602Trp(p.R602W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript