Colon Cancer: Gene >> MAEA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303400
Start	1312044:1312044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135C>G
AA Mutation	p.Ser45Arg(p.S45R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303400
Start	1315524:1315524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758614928
CDS Mutation	c.380G>A
AA Mutation	p.Arg127His(p.R127H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303400
Start	1338532:1338532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010G>A
AA Mutation	p.Arg337His(p.R337H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000303400
Start	1322387:1322387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768054350
CDS Mutation	c.463G>C
AA Mutation	p.Val155Leu(p.V155L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000303400
Start	1332846:1332846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746C>T
AA Mutation	p.Thr249Met(p.T249M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000303400
Start	1315515:1315515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765652453
CDS Mutation	c.371G>A
AA Mutation	p.Arg124His(p.R124H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303400
Start	1327671:1327671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303400
Start	1312107:1312107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765489677
CDS Mutation	c.198C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303400
Start	1312047:1312047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751359580
CDS Mutation	c.138C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAEA

No Mutation Annotation!