Colon Cancer: Gene >> TXNRD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400521
Start	19878121:19878121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766076027
CDS Mutation	c.1414G>A
AA Mutation	p.Glu472Lys(p.E472K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000400521
Start	19915221:19915221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584C>A
AA Mutation	p.Pro195His(p.P195H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000400521
Start	19895508:19895508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531699366
CDS Mutation	c.848G>A
AA Mutation	p.Arg283Gln(p.R283Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000400521
Start	19880235:19880235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1219T>C
AA Mutation	p.Cys407Arg(p.C407R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000400521
Start	19878139:19878139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1396C>A
AA Mutation	p.Leu466Ile(p.L466I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000400521
Start	19880663:19880663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377714537
CDS Mutation	c.1141C>T
AA Mutation	p.Arg381Trp(p.R381W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000400521
Start	19878403:19878403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1310C>T
AA Mutation	p.Thr437Met(p.T437M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400521
Start	19898099:19898099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202225486
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400521
Start	19915262:19915262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367754522
CDS Mutation	c.543C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400521
Start	19878165:19878165(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1370delC
AA Mutation	p.Pro457HisfsTer34(p.P457Hfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TXNRD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400521
Start	19915787:19915787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506G>A
AA Mutation	p.Gly169Asp(p.G169D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000400521
Start	19911379:19911379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.660A>C
AA Mutation	p.Lys220Asn(p.K220N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript