Colon Cancer: Gene >> TIMELESS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000553532
Start	56418226:56418226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3362C>G
AA Mutation	p.Ser1121Cys(p.S1121C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000553532
Start	56422976:56422976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2309C>T
AA Mutation	p.Ala770Val(p.A770V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000553532
Start	56434158:56434158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.13A>G
AA Mutation	p.Met5Val(p.M5V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000553532
Start	56420589:56420589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145031140
CDS Mutation	c.3208C>T
AA Mutation	p.Arg1070Trp(p.R1070W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000553532
Start	56432482:56432482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.574G>T
AA Mutation	p.Ala192Ser(p.A192S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000553532
Start	56432509:56432509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781372283
CDS Mutation	c.547G>A
AA Mutation	p.Ala183Thr(p.A183T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000553532
Start	56421924:56421924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2617G>A
AA Mutation	p.Ala873Thr(p.A873T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000553532
Start	56420673:56420673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745492833
CDS Mutation	c.3124G>A
AA Mutation	p.Val1042Ile(p.V1042I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000553532
Start	56423375:56423375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770377436
CDS Mutation	c.2191C>T
AA Mutation	p.Arg731Trp(p.R731W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000553532
Start	56420604:56420604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371723339
CDS Mutation	c.3193C>T
AA Mutation	p.Arg1065Cys(p.R1065C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000553532
Start	56429062:56429062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000553532
Start	56423649:56423649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2025A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000553532
Start	56420817:56420817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3105G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000553532
Start	56424887:56424887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1743G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000553532
Start	56423420:56423420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2146C>T
AA Mutation	p.Gln716Ter(p.Q716*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000553532
Start	56428355:56428355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747106203
CDS Mutation	c.1459C>T
AA Mutation	p.Arg487Ter(p.R487*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000553532
Start	56418009:56418009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3455-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TIMELESS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000553532
Start	56420839:56420839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763159822
CDS Mutation	c.3083G>A
AA Mutation	p.Arg1028Gln(p.R1028Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000553532
Start	56423703:56423703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1971G>A
Mutation Classification	Silent
Feature Type	Transcript