Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> PRG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287143
Start	57379537:57379537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779423526
CDS Mutation	c.332G>A
AA Mutation	p.Arg111His(p.R111H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287143
Start	57379498:57379498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371C>T
AA Mutation	p.Ala124Val(p.A124V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287143
Start	57379764:57379764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.105C>A
AA Mutation	p.Asp35Glu(p.D35E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000287143
Start	57378681:57378681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507G>C
AA Mutation	p.Trp169Cys(p.W169C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287143
Start	57376896:57376896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756413130
CDS Mutation	c.632G>A
AA Mutation	p.Arg211Gln(p.R211Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287143
Start	57380653:57380653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.56A>G
AA Mutation	p.His19Arg(p.H19R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287143
Start	57379793:57379793(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776957765
CDS Mutation	c.76delC
AA Mutation	p.His26IlefsTer5(p.H26Ifs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PRG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287143
Start	57379537:57379537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779423526
CDS Mutation	c.332G>A
AA Mutation	p.Arg111His(p.R111H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287143
Start	57378786:57378786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.402C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287143
Start	57376883:57376883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript