Colon Cancer: Gene >> CNR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88145021:88145021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254C>A
AA Mutation	p.Ser85Tyr(p.S85Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144133:88144133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142T>G
AA Mutation	p.Phe381Cys(p.F381C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144422:88144422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199892728
CDS Mutation	c.853G>A
AA Mutation	p.Val285Ile(p.V285I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144290:88144290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.985G>A
AA Mutation	p.Val329Met(p.V329M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88143968:88143968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1307C>A
AA Mutation	p.Ala436Glu(p.A436E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144796:88144796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759310920
CDS Mutation	c.479C>T
AA Mutation	p.Ala160Val(p.A160V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144049:88144049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143455045
CDS Mutation	c.1226G>A
AA Mutation	p.Arg409Gln(p.R409Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144145:88144145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764560714
CDS Mutation	c.1130C>T
AA Mutation	p.Thr377Met(p.T377M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144901:88144901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.374C>T
AA Mutation	p.Thr125Met(p.T125M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144355:88144355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140913272
CDS Mutation	c.920G>A
AA Mutation	p.Arg307His(p.R307H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88145184:88145184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770413069
CDS Mutation	c.91G>A
AA Mutation	p.Glu31Lys(p.E31K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144061:88144061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1214G>A
AA Mutation	p.Arg405Gln(p.R405Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144832:88144832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443G>A
AA Mutation	p.Arg148His(p.R148H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369499
Start	88143988:88143988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149238893
CDS Mutation	c.1287G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369499
Start	88144567:88144567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577054667
CDS Mutation	c.708G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369499
Start	88145185:88145185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774890934
CDS Mutation	c.90C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369499
Start	88144666:88144666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000369499
Start	88144062:88144062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770859974
CDS Mutation	c.1213C>T
AA Mutation	p.Arg405Ter(p.R405*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CNR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144841:88144841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143463104
CDS Mutation	c.434G>A
AA Mutation	p.Arg145His(p.R145H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88145189:88145189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.86A>G
AA Mutation	p.Gln29Arg(p.Q29R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369499
Start	88144351:88144351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.924G>T
AA Mutation	p.Met308Ile(p.M308I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369499
Start	88144531:88144531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762643235
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript