Colon Cancer: Gene >> DTX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324432
Start	76480519:76480519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.10G>T
AA Mutation	p.Ala4Ser(p.A4S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324432
Start	76482910:76482910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671A>G
AA Mutation	p.Tyr224Cys(p.Y224C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324432
Start	76482759:76482759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138102519
CDS Mutation	c.520C>T
AA Mutation	p.Arg174Cys(p.R174C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324432
Start	76497389:76497389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761188367
CDS Mutation	c.1062C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324432
Start	76505457:76505457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756074116
CDS Mutation	c.1725C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000324432
Start	76482921:76482921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.682C>T
AA Mutation	p.Gln228Ter(p.Q228*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DTX2

No Mutation Annotation!