Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MEPE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361056
Start	87846310:87846310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138152179
CDS Mutation	c.1442G>A
AA Mutation	p.Arg481Gln(p.R481Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361056
Start	87845699:87845699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831A>C
AA Mutation	p.Glu277Asp(p.E277D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361056
Start	87845452:87845452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584A>C
AA Mutation	p.Lys195Thr(p.K195T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361056
Start	87846394:87846394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1526A>G
AA Mutation	p.Asp509Gly(p.D509G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361056
Start	87845839:87845839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113931822
CDS Mutation	c.971C>T
AA Mutation	p.Ala324Val(p.A324V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361056
Start	87846067:87846067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1199C>A
AA Mutation	p.Pro400His(p.P400H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361056
Start	87845440:87845440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773178722
CDS Mutation	c.572C>T
AA Mutation	p.Ser191Leu(p.S191L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361056
Start	87846213:87846213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1345A>C
AA Mutation	p.Asn449His(p.N449H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361056
Start	87838684:87838684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107G>A
AA Mutation	p.Arg36Lys(p.R36K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361056
Start	87845348:87845348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374913233
CDS Mutation	c.480G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361056
Start	87845297:87845297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145299039
CDS Mutation	c.429C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361056
Start	87845834:87845834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.966A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361056
Start	87846230:87846230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1362T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MEPE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361056
Start	87846310:87846310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138152179
CDS Mutation	c.1442G>A
AA Mutation	p.Arg481Gln(p.R481Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361056
Start	87845298:87845298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148637496
CDS Mutation	c.430G>A
AA Mutation	p.Ala144Thr(p.A144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361056
Start	87845239:87845239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371A>G
AA Mutation	p.Lys124Arg(p.K124R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript