Colon Cancer: Gene >> CRTC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321949
Start	18743007:18743007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224C>T
AA Mutation	p.Thr75Ile(p.T75I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321949
Start	18745928:18745928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Trp(p.R117W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321949
Start	18745901:18745901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322C>T
AA Mutation	p.Arg108Cys(p.R108C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321949
Start	18683710:18683710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>T
AA Mutation	p.Thr3Ile(p.T3I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321949
Start	18771464:18771464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748706628
CDS Mutation	c.1343G>A
AA Mutation	p.Arg448His(p.R448H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321949
Start	18749829:18749829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321949
Start	18749820:18749820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765028098
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321949
Start	18765453:18765453(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.940delC
AA Mutation	p.Leu314CysfsTer3(p.L314Cfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321949
Start	18777183:18777184(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1712_1713delCC
AA Mutation	p.Pro571GlnfsTer4(p.P571Qfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321949
Start	18768744:18768744(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1277delC
AA Mutation	p.Pro426GlnfsTer85(p.P426Qfs*85)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321949
Start	18777183:18777183(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs779900748
CDS Mutation	c.1713delC
AA Mutation	p.Ser572AlafsTer6(p.S572Afs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321949
Start	18760031:18760031(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.692delA
AA Mutation	p.Asn231ThrfsTer5(p.N231Tfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321949
Start	18760069:18760069(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.732delG
AA Mutation	p.Ser245ProfsTer5(p.S245Pfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321949
Start	18768649:18768650(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1181dupC
AA Mutation	p.Gly395TrpfsTer56(p.G395Wfs*56)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321949
Start	18768743:18768744(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs760791352
CDS Mutation	c.1277dupC
AA Mutation	p.Glu427ArgfsTer24(p.E427Rfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CRTC1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321949
Start	18765450:18765450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.933C>T
Mutation Classification	Silent
Feature Type	Transcript