Colon Cancer: Gene >> CYP39A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275016
Start	46550415:46550415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1361T>C
AA Mutation	p.Val454Ala(p.V454A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275016
Start	46631059:46631059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.744A>C
AA Mutation	p.Gln248His(p.Q248H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000275016
Start	46596043:46596043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201855604
CDS Mutation	c.1009C>T
AA Mutation	p.Arg337Cys(p.R337C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000275016
Start	46642261:46642261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215G>A
AA Mutation	p.Arg72Gln(p.R72Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000275016
Start	46652566:46652566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.17C>T
AA Mutation	p.Pro6Leu(p.P6L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275016
Start	46550414:46550414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1362C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275016
Start	46639649:46639649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.333C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CYP39A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275016
Start	46550391:46550391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767237937
CDS Mutation	c.1385G>A
AA Mutation	p.Arg462Gln(p.R462Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000275016
Start	46652432:46652432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151G>T
AA Mutation	p.Glu51Ter(p.E51*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript