Colon Cancer: Gene >> FSIP1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000350221
Start	39770429:39770429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308C>T
AA Mutation	p.Ser103Leu(p.S103L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350221
Start	39726594:39726594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1045A>G
AA Mutation	p.Asn349Asp(p.N349D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350221
Start	39617858:39617858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1576A>G
AA Mutation	p.Thr526Ala(p.T526A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350221
Start	39617863:39617863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759273718
CDS Mutation	c.1571C>T
AA Mutation	p.Ser524Leu(p.S524L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350221
Start	39765627:39765627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430C>G
AA Mutation	p.Leu144Val(p.L144V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350221
Start	39617881:39617881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1553C>T
AA Mutation	p.Thr518Ile(p.T518I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000350221
Start	39765729:39765729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.328G>T
AA Mutation	p.Glu110Ter(p.E110*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FSIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350221
Start	39617810:39617810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1624C>G
AA Mutation	p.Leu542Val(p.L542V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350221
Start	39618035:39618035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1399G>T
AA Mutation	p.Asp467Tyr(p.D467Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350221
Start	39738185:39738185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.797G>T
AA Mutation	p.Arg266Ile(p.R266I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350221
Start	39765684:39765684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373C>A
AA Mutation	p.Leu125Ile(p.L125I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350221
Start	39600916:39600916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1710G>A
Mutation Classification	Silent
Feature Type	Transcript