Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FOLR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298223
Start	72218661:72218661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.77A>C
AA Mutation	p.Asp26Ala(p.D26A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298223
Start	72221548:72221548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554G>C
AA Mutation	p.Gly185Ala(p.G185A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298223
Start	72221571:72221571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.577G>A
AA Mutation	p.Val193Ile(p.V193I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298223
Start	72221192:72221192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193165102
CDS Mutation	c.356G>A
AA Mutation	p.Arg119His(p.R119H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298223
Start	72218629:72218629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.45A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298223
Start	72218641:72218641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FOLR2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298223
Start	72220929:72220929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.210G>T
AA Mutation	p.Lys70Asn(p.K70N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298223
Start	72221654:72221654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs1803567
CDS Mutation	c.660G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000298223
Start	72221197:72221197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>T
AA Mutation	p.Glu121Ter(p.E121*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript