Colon Cancer: Gene >> F2RL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296641
Start	76617830:76617830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877G>A
AA Mutation	p.Asp293Asn(p.D293N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296641
Start	76617624:76617624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1083G>A
AA Mutation	p.Met361Ile(p.M361I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000296641
Start	76618204:76618204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503C>T
AA Mutation	p.Ala168Val(p.A168V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000296641
Start	76618121:76618121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150312521
CDS Mutation	c.586G>A
AA Mutation	p.Val196Ile(p.V196I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000296641
Start	76618635:76618635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.72A>C
AA Mutation	p.Glu24Asp(p.E24D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296641
Start	76617939:76617939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.768T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000296641
Start	76617936:76617936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.771C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> F2RL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000296641
Start	76617631:76617631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1076T>G
AA Mutation	p.Phe359Cys(p.F359C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000296641
Start	76618567:76618567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140C>A
AA Mutation	p.Ser47Tyr(p.S47Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript