Colon Cancer: Gene >> CLOCK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309964
Start	55456278:55456278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815C>T
AA Mutation	p.Pro272Leu(p.P272L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309964
Start	55438288:55438288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2355T>G
AA Mutation	p.Phe785Leu(p.F785L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309964
Start	55478896:55478896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.175T>C
AA Mutation	p.Ser59Pro(p.S59P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309964
Start	55476018:55476018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.293A>G
AA Mutation	p.Gln98Arg(p.Q98R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309964
Start	55453703:55453703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1104T>A
AA Mutation	p.Phe368Leu(p.F368L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000309964
Start	55448858:55448858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779397098
CDS Mutation	c.1460C>T
AA Mutation	p.Ser487Phe(p.S487F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000309964
Start	55458978:55458978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.706A>G
AA Mutation	p.Thr236Ala(p.T236A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000309964
Start	55456218:55456218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.875G>T
AA Mutation	p.Arg292Met(p.R292M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309964
Start	55450110:55450110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309964
Start	55442611:55442611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1926G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309964
Start	55459203:55459203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000309964
Start	55478827:55478827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244C>T
AA Mutation	p.Arg82Ter(p.R82*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000309964
Start	55450120:55450120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1319C>A
AA Mutation	p.Ser440Ter(p.S440*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309964
Start	55459254:55459255(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.566dupA
AA Mutation	p.Asn189LysfsTer23(p.N189Kfs*23)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309964
Start	55470786:55470787(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs758547642
CDS Mutation	c.368dupT
AA Mutation	p.Leu123PhefsTer14(p.L123Ffs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000309964
Start	55435596:55435596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2362-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CLOCK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309964
Start	55438509:55438509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2134A>G
AA Mutation	p.Lys712Glu(p.K712E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309964
Start	55459159:55459159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662C>A
AA Mutation	p.Ser221Tyr(p.S221Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309964
Start	55478926:55478926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.145C>A
AA Mutation	p.Gln49Lys(p.Q49K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript