Colon Cancer: Gene >> ISYNA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338128
Start	18436340:18436340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.749G>A
AA Mutation	p.Arg250His(p.R250H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338128
Start	18435351:18435351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1387C>A
AA Mutation	p.Leu463Ile(p.L463I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338128
Start	18435372:18435372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758356975
CDS Mutation	c.1366G>A
AA Mutation	p.Val456Met(p.V456M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338128
Start	18436045:18436045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.962G>A
AA Mutation	p.Gly321Asp(p.G321D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338128
Start	18437018:18437018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.370A>G
AA Mutation	p.Ser124Gly(p.S124G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000338128
Start	18436178:18436178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829A>G
AA Mutation	p.Asn277Asp(p.N277D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338128
Start	18435817:18435817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1080G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338128
Start	18435781:18435781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338128
Start	18436717:18436717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.576G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338128
Start	18436792:18436792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338128
Start	18436405:18436405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779370907
CDS Mutation	c.684G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000338128
Start	18436031:18436031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ISYNA1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338128
Start	18436983:18436983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405C>T
Mutation Classification	Silent
Feature Type	Transcript