Colon Cancer: Gene >> AZIN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294517
Start	33094606:33094606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144776558
CDS Mutation	c.646G>A
AA Mutation	p.Ala216Thr(p.A216T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294517
Start	33082254:33082254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5C>T
AA Mutation	p.Ala2Val(p.A2V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294517
Start	33094565:33094565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605G>A
AA Mutation	p.Gly202Asp(p.G202D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294517
Start	33118064:33118064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1192T>C
AA Mutation	p.Phe398Leu(p.F398L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294517
Start	33092103:33092103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192729842
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294517
Start	33084026:33084026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.178C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294517
Start	33084080:33084080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AZIN2

No Mutation Annotation!