Colon Cancer: Gene >> CYP1A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343932
Start	74754847:74754847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1310G>A
AA Mutation	p.Gly437Asp(p.G437D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343932
Start	74750007:74750007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201551575
CDS Mutation	c.269G>A
AA Mutation	p.Arg90His(p.R90H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343932
Start	74751208:74751208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368776150
CDS Mutation	c.851C>T
AA Mutation	p.Thr284Met(p.T284M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343932
Start	74755041:74755041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1504G>A
AA Mutation	p.Ala502Thr(p.A502T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343932
Start	74750037:74750037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201650099
CDS Mutation	c.299G>A
AA Mutation	p.Arg100Gln(p.R100Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000343932
Start	74749973:74749973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761941661
CDS Mutation	c.235C>T
AA Mutation	p.Arg79Cys(p.R79C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000343932
Start	74755000:74755000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1463A>T
AA Mutation	p.Lys488Ile(p.K488I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000343932
Start	74750006:74750006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556218799
CDS Mutation	c.268C>T
AA Mutation	p.Arg90Cys(p.R90C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343932
Start	74753232:74753232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1215C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343932
Start	74753238:74753238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1221C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000343932
Start	74751222:74751222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.865A>T
AA Mutation	p.Lys289Ter(p.K289*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000343932
Start	74753254:74753254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1237C>T
AA Mutation	p.Gln413Ter(p.Q413*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CYP1A2

No Mutation Annotation!