Colon Cancer: Gene >> DDX39A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242776
Start	14410244:14410244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704G>A
AA Mutation	p.Arg235Gln(p.R235Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242776
Start	14409442:14409442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.980C>T
AA Mutation	p.Ser327Leu(p.S327L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242776
Start	14410278:14410278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670A>G
AA Mutation	p.Met224Val(p.M224V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242776
Start	14411528:14411528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.407C>T
AA Mutation	p.Ser136Phe(p.S136F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242776
Start	14413080:14413080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242776
Start	14409634:14409634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371615674
CDS Mutation	c.876C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242776
Start	14411539:14411539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.396T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> DDX39A

No Mutation Annotation!