Colon Cancer: Gene >> GAD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259271
Start	26286445:26286445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1337G>A
AA Mutation	p.Cys446Tyr(p.C446Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259271
Start	26292484:26292484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1406C>T
AA Mutation	p.Ala469Val(p.A469V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000259271
Start	26217610:26217610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.77C>T
AA Mutation	p.Ala26Val(p.A26V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000259271
Start	26216885:26216885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.76G>T
AA Mutation	p.Ala26Ser(p.A26S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000259271
Start	26286451:26286451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1343G>A
AA Mutation	p.Arg448His(p.R448H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000259271
Start	26245967:26245967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.887C>A
AA Mutation	p.Thr296Lys(p.T296K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000259271
Start	26219055:26219055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299C>T
AA Mutation	p.Ala100Val(p.A100V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000259271
Start	26217615:26217615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82G>A
AA Mutation	p.Ala28Thr(p.A28T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000259271
Start	26300872:26300872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1669T>C
AA Mutation	p.Phe557Leu(p.F557L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000259271
Start	26216862:26216862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776361193
CDS Mutation	c.53G>T
AA Mutation	p.Gly18Val(p.G18V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259271
Start	26273689:26273689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259271
Start	26219053:26219053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772863932
CDS Mutation	c.297G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GAD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259271
Start	26300922:26300922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1719C>A
AA Mutation	p.Phe573Leu(p.F573L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259271
Start	26217631:26217631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98C>A
AA Mutation	p.Ala33Asp(p.A33D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259271
Start	26245931:26245931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.851C>A
AA Mutation	p.Ser284Tyr(p.S284Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259271
Start	26292988:26292988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763555415
CDS Mutation	c.1581G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259271
Start	26281055:26281055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1204T>C
Mutation Classification	Silent
Feature Type	Transcript