Colon Cancer: Gene >> UPF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18832309:18832309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100G>A
AA Mutation	p.Glu34Lys(p.E34K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18854607:18854607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196G>A
AA Mutation	p.Gly399Asp(p.G399D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18860878:18860878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2386G>A
AA Mutation	p.Ala796Thr(p.A796T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18860962:18860962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2470C>A
AA Mutation	p.Leu824Met(p.L824M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18857348:18857348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2030T>C
AA Mutation	p.Leu677Pro(p.L677P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18856943:18856943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367803735
CDS Mutation	c.1924C>T
AA Mutation	p.Arg642Cys(p.R642C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18862125:18862125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2606G>A
AA Mutation	p.Arg869His(p.R869H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18865755:18865755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3247C>A
AA Mutation	p.Leu1083Ile(p.L1083I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18847814:18847814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Cys(p.R148C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18856263:18856263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1820G>A
AA Mutation	p.Arg607Gln(p.R607Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18864177:18864177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2816G>A
AA Mutation	p.Arg939His(p.R939H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18854622:18854622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1211T>C
AA Mutation	p.Ile404Thr(p.I404T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18856280:18856280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1837G>A
AA Mutation	p.Ala613Thr(p.A613T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18857473:18857473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2155C>T
AA Mutation	p.Leu719Phe(p.L719F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18850821:18850821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763C>T
AA Mutation	p.Arg255Cys(p.R255C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18863450:18863450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2646C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18857502:18857502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759452259
CDS Mutation	c.2184C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18832239:18832239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.30G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18846093:18846093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.345G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18865598:18865598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3090A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18846006:18846006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149711534
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> UPF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18856944:18856944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1925G>A
AA Mutation	p.Arg642His(p.R642H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000599848
Start	18856961:18856961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1942G>A
AA Mutation	p.Glu648Lys(p.E648K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000599848
Start	18863444:18863444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758737674
CDS Mutation	c.2640C>T
Mutation Classification	Silent
Feature Type	Transcript