Colon Cancer: Gene >> CRTC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368633
Start	153951378:153951378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377025190
CDS Mutation	c.1286G>A
AA Mutation	p.Arg429His(p.R429H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368633
Start	153951348:153951348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779135391
CDS Mutation	c.1316C>T
AA Mutation	p.Ala439Val(p.A439V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368633
Start	153951528:153951528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143226168
CDS Mutation	c.1136G>A
AA Mutation	p.Arg379His(p.R379H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368633
Start	153951297:153951297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754577717
CDS Mutation	c.1367C>T
AA Mutation	p.Ser456Leu(p.S456L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368633
Start	153951382:153951382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282C>T
AA Mutation	p.Arg428Cys(p.R428C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368633
Start	153951428:153951428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201148360
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368633
Start	153952408:153952408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.741C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368633
Start	153951338:153951338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145272706
CDS Mutation	c.1326C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368633
Start	153951388:153951388(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1276delC
AA Mutation	p.His426ThrfsTer10(p.H426Tfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CRTC2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368633
Start	153952616:153952616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657C>A
AA Mutation	p.Asn219Lys(p.N219K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368633
Start	153949345:153949345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753578803
CDS Mutation	c.1444C>T
AA Mutation	p.Arg482Trp(p.R482W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368633
Start	153951297:153951297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754577717
CDS Mutation	c.1367C>T
AA Mutation	p.Ser456Leu(p.S456L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368633
Start	153952616:153952616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript