Colon Cancer: Gene >> DUOXA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323030
Start	45116723:45116723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.548C>T
AA Mutation	p.Thr183Met(p.T183M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323030
Start	45116593:45116593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>A
AA Mutation	p.Ala140Thr(p.A140T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323030
Start	45114673:45114673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.68C>T
AA Mutation	p.Pro23Leu(p.P23L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323030
Start	45115826:45115826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.175C>A
AA Mutation	p.Leu59Ile(p.L59I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323030
Start	45114683:45114683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323030
Start	45116215:45116215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323030
Start	45117097:45117097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323030
Start	45114683:45114683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323030
Start	45117891:45117891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.945T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DUOXA2

No Mutation Annotation!