Colon Cancer: Gene >> AANAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392492
Start	76468777:76468777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31C>T
AA Mutation	p.Pro11Ser(p.P11S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392492
Start	76469803:76469803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576095033
CDS Mutation	c.457G>A
AA Mutation	p.Val153Met(p.V153M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392492
Start	76469193:76469193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201200092
CDS Mutation	c.184G>A
AA Mutation	p.Val62Ile(p.V62I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392492
Start	76468854:76468854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746533176
CDS Mutation	c.108G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392492
Start	76469237:76469237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771430665
CDS Mutation	c.228A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392492
Start	76469730:76469730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200468284
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000392492
Start	76469740:76469740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.394C>T
AA Mutation	p.Gln132Ter(p.Q132*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AANAT

No Mutation Annotation!