Colon Cancer: Gene >> GSN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373818
Start	121302998:121302998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437A>G
AA Mutation	p.His146Arg(p.H146R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373818
Start	121310819:121310819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121909715
CDS Mutation	c.640G>A
AA Mutation	p.Asp214Asn(p.D214N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373818
Start	121326558:121326558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1616T>C
AA Mutation	p.Phe539Ser(p.F539S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373818
Start	121310790:121310790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611C>A
AA Mutation	p.Pro204His(p.P204H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373818
Start	121332574:121332574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2320G>T
AA Mutation	p.Asp774Tyr(p.D774Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373818
Start	121313995:121313995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878C>T
AA Mutation	p.Ala293Val(p.A293V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373818
Start	121302942:121302942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761824852
CDS Mutation	c.381G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373818
Start	121332489:121332489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2235C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373818
Start	121317187:121317187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374571846
CDS Mutation	c.1008C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373818
Start	121326607:121326607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745619898
CDS Mutation	c.1665C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000373818
Start	121329016:121329016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2040+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> GSN

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373818
Start	121312422:121312422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146329975
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript