Colon Cancer: Gene >> FBLN5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342058
Start	91877555:91877555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1117C>A
AA Mutation	p.Arg373Ser(p.R373S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000342058
Start	91936958:91936958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.368A>G
AA Mutation	p.Asn123Ser(p.N123S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000342058
Start	91891274:91891274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.566C>A
AA Mutation	p.Ser189Tyr(p.S189Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342058
Start	91881381:91881381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342058
Start	91883069:91883069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554422450
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FBLN5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342058
Start	91877611:91877611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1061A>G
AA Mutation	p.Asp354Gly(p.D354G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript