Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GDNF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326524
Start	37815800:37815800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753300953
CDS Mutation	c.487T>G
AA Mutation	p.Leu163Val(p.L163V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326524
Start	37815936:37815936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.351T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326524
Start	37816104:37816104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115263690
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326524
Start	37815840:37815840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368244196
CDS Mutation	c.447C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326524
Start	37815819:37815819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561764524
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326524
Start	37815930:37815930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326524
Start	37834746:37834746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.51G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GDNF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000326524
Start	37816099:37816099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.188A>T
AA Mutation	p.Asp63Val(p.D63V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000326524
Start	37815862:37815862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.425T>G
AA Mutation	p.Phe142Cys(p.F142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326524
Start	37815840:37815840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368244196
CDS Mutation	c.447C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000326524
Start	37816104:37816104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115263690
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript