Colon Cancer: Gene >> CRY1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000008527
Start	106999810:106999810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772585429
CDS Mutation	c.878G>A
AA Mutation	p.Arg293His(p.R293H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000008527
Start	106997619:106997619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1361T>A
AA Mutation	p.Ile454Asn(p.I454N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000008527
Start	106997955:106997955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770965692
CDS Mutation	c.1249G>A
AA Mutation	p.Gly417Ser(p.G417S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000008527
Start	106999646:106999646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749506981
CDS Mutation	c.1042C>T
AA Mutation	p.Arg348Cys(p.R348C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000008527
Start	107000045:107000045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.722C>T
AA Mutation	p.Ala241Val(p.A241V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000008527
Start	107001311:107001311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.653T>G
AA Mutation	p.Leu218Arg(p.L218R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000008527
Start	107005136:107005136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380G>T
AA Mutation	p.Arg127Ile(p.R127I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000008527
Start	107092863:107092863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000008527
Start	106997537:106997537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368170196
CDS Mutation	c.1443C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000008527
Start	107005180:107005180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000008527
Start	107001300:107001300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664G>T
AA Mutation	p.Glu222Ter(p.E222*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CRY1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000008527
Start	106999768:106999768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920A>G
AA Mutation	p.Asp307Gly(p.D307G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000008527
Start	107092877:107092877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85G>A
AA Mutation	p.Asp29Asn(p.D29N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000008527
Start	107022160:107022160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.191C>G
AA Mutation	p.Ala64Gly(p.A64G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000008527
Start	107022184:107022184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.167T>G
AA Mutation	p.Leu56Arg(p.L56R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000008527
Start	106992996:106992996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1626C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000008527
Start	106999980:106999980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.787C>T
AA Mutation	p.Arg263Ter(p.R263*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript