Colon Cancer: Gene >> CREB5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357727
Start	28809310:28809310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1150C>T
AA Mutation	p.Arg384Trp(p.R384W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357727
Start	28570386:28570386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313G>A
AA Mutation	p.Val105Ile(p.V105I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357727
Start	28804308:28804308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.812A>G
AA Mutation	p.His271Arg(p.H271R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357727
Start	28570435:28570435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116248568
CDS Mutation	c.362G>A
AA Mutation	p.Arg121Gln(p.R121Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357727
Start	28570480:28570480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555693522
CDS Mutation	c.407C>T
AA Mutation	p.Pro136Leu(p.P136L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357727
Start	28809203:28809203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1043A>G
AA Mutation	p.Gln348Arg(p.Q348R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357727
Start	28818102:28818102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1286C>A
AA Mutation	p.Ala429Asp(p.A429D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357727
Start	28570403:28570403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537303404
CDS Mutation	c.330G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357727
Start	28507674:28507674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357727
Start	28804285:28804285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.789C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357727
Start	28570394:28570394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.321G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357727
Start	28804303:28804303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573375434
CDS Mutation	c.807G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357727
Start	28570409:28570409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370145745
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000357727
Start	28804278:28804279(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.782_783insTTAAAA
AA Mutation	p.Met261delinsIleTerLys(p.M261delinsI*K)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357727
Start	28804279:28804280(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.783_784insCAAA
AA Mutation	p.Met262GlnfsTer160(p.M262Qfs*160)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000357727
Start	28818070:28818070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1255-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CREB5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357727
Start	28488192:28488192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21G>T
AA Mutation	p.Lys7Asn(p.K7N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000357727
Start	28507735:28507735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766189534
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Trp(p.R97W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357727
Start	28809304:28809304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1144C>A
AA Mutation	p.Leu382Met(p.L382M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript