Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDH3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264012
Start	68682398:68682398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1093A>C
AA Mutation	p.Thr365Pro(p.T365P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264012
Start	68687731:68687731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1790A>C
AA Mutation	p.Glu597Ala(p.E597A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264012
Start	68698354:68698354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557740168
CDS Mutation	c.2444G>A
AA Mutation	p.Arg815His(p.R815H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000264012
Start	68682487:68682487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182G>T
AA Mutation	p.Lys394Asn(p.K394N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264012
Start	68678547:68678547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200463078
CDS Mutation	c.437C>T
AA Mutation	p.Thr146Met(p.T146M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264012
Start	68687542:68687542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1601T>C
AA Mutation	p.Leu534Pro(p.L534P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264012
Start	68684797:68684797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1397A>G
AA Mutation	p.Asp466Gly(p.D466G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264012
Start	68687562:68687562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621G>A
AA Mutation	p.Val541Ile(p.V541I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264012
Start	68695905:68695905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776565426
CDS Mutation	c.2262C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264012
Start	68687729:68687729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764866365
CDS Mutation	c.1788C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_lost
Transcription ID	ENST00000264012
Start	68698398:68698398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2488T>C
AA Mutation	p.Ter830GlnextTer37(p.830Qext37)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CDH3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264012
Start	68695905:68695905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776565426
CDS Mutation	c.2262C>T
Mutation Classification	Silent
Feature Type	Transcript