Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CADM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222374
Start	43625167:43625167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.839G>A
AA Mutation	p.Gly280Asp(p.G280D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222374
Start	43627235:43627235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.295G>A
AA Mutation	p.Glu99Lys(p.E99K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222374
Start	43626889:43626889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394C>T
AA Mutation	p.Arg132Trp(p.R132W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000222374
Start	43626288:43626288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500G>A
AA Mutation	p.Gly167Glu(p.G167E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222374
Start	43627193:43627193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.337C>A
AA Mutation	p.His113Asn(p.H113N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222374
Start	43623363:43623363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144737031
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CADM4

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000222374
Start	43627644:43627644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.211G>C
AA Mutation	p.Ala71Pro(p.A71P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222374
Start	43627674:43627674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.181C>T
AA Mutation	p.Arg61Trp(p.R61W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222374
Start	43626888:43626888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.395G>A
AA Mutation	p.Arg132Gln(p.R132Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript