Colon Cancer: Gene >> GZMA

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000274306
Start	55107794:55107794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.216G>T
AA Mutation	p.Leu72Phe(p.L72F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274306
Start	55107872:55107872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294G>T
AA Mutation	p.Lys98Asn(p.K98N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000274306
Start	55107935:55107935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.357G>T
AA Mutation	p.Gln119His(p.Q119H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274306
Start	55108147:55108147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380A>G
AA Mutation	p.Asn127Ser(p.N127S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000274306
Start	55107834:55107834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256A>G
AA Mutation	p.Thr86Ala(p.T86A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000274306
Start	55107804:55107804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765136087
CDS Mutation	c.226T>C
AA Mutation	p.Ser76Pro(p.S76P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000274306
Start	55105567:55105567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164C>A
AA Mutation	p.Ala55Asp(p.A55D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274306
Start	55110095:55110095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371339546
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274306
Start	55110047:55110047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374569624
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GZMA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274306
Start	55105489:55105489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86T>A
AA Mutation	p.Ile29Asn(p.I29N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274306
Start	55107816:55107816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238C>A
AA Mutation	p.Leu80Ile(p.L80I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274306
Start	55108324:55108324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.557A>G
AA Mutation	p.Asn186Ser(p.N186S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274306
Start	55110095:55110095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371339546
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript