Colon Cancer: Gene >> FICD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000552695
Start	108519266:108519266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1168A>G
AA Mutation	p.Thr390Ala(p.T390A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000552695
Start	108517102:108517102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130C>A
AA Mutation	p.Leu44Met(p.L44M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000552695
Start	108519281:108519281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1183C>A
AA Mutation	p.Gln395Lys(p.Q395K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000552695
Start	108519032:108519032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934A>G
AA Mutation	p.Thr312Ala(p.T312A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000552695
Start	108519325:108519325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763816141
CDS Mutation	c.1227C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000552695
Start	108518515:108518515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200978347
CDS Mutation	c.417C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000552695
Start	108517197:108517197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.225C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000552695
Start	108518426:108518426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000552695
Start	108519205:108519205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536678902
CDS Mutation	c.1107C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000552695
Start	108517055:108517056(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.83_84insTTCA
AA Mutation	p.Leu29SerfsTer76(p.L29Sfs*76)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FICD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000552695
Start	108519326:108519326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775969172
CDS Mutation	c.1228G>A
AA Mutation	p.Asp410Asn(p.D410N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript