Colon Cancer: Gene >> TARBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266987
Start	53504758:53504758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556C>A
AA Mutation	p.Pro186Thr(p.P186T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266987
Start	53506089:53506089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747821228
CDS Mutation	c.1042C>T
AA Mutation	p.Arg348Cys(p.R348C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266987
Start	53504404:53504404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139126157
CDS Mutation	c.430C>G
AA Mutation	p.Pro144Ala(p.P144A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266987
Start	53504792:53504792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.590G>A
AA Mutation	p.Arg197Gln(p.R197Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266987
Start	53504723:53504723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.521G>A
AA Mutation	p.Arg174Gln(p.R174Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266987
Start	53505174:53505174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.653C>T
AA Mutation	p.Ala218Val(p.A218V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266987
Start	53505194:53505194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.673G>A
AA Mutation	p.Val225Met(p.V225M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266987
Start	53503725:53503725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266987
Start	53504730:53504730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200766710
CDS Mutation	c.528G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266987
Start	53502168:53502168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.207C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000266987
Start	53504773:53504773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571G>T
AA Mutation	p.Glu191Ter(p.E191*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000266987
Start	53505676:53505676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758198296
CDS Mutation	c.769C>T
AA Mutation	p.Arg257Ter(p.R257*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000266987
Start	53503131:53503131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.326+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TARBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266987
Start	53505677:53505677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.770G>A
AA Mutation	p.Arg257Gln(p.R257Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266987
Start	53505158:53505158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.637G>A
AA Mutation	p.Ala213Thr(p.A213T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266987
Start	53504784:53504784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582G>T
AA Mutation	p.Met194Ile(p.M194I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript