Colon Cancer: Gene >> POLR2F

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000427034
Start	38025913:38025913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.159A>G
AA Mutation	p.Thr54Ala(p.T54A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442738
Start	37959448:37959448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760223334
CDS Mutation	c.193G>A
AA Mutation	p.Val65Met(p.V65M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000333418
Start	38025871:38025871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.123C>T
AA Mutation	p.Ala42Val(p.A42V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000442738
Start	37967642:37967642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311T>C
AA Mutation	p.Ile104Thr(p.I104T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000442738
Start	37956837:37956837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771399849
CDS Mutation	c.85G>A
AA Mutation	p.Glu29Lys(p.E29K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000442738
Start	37959445:37959445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.190C>T
AA Mutation	p.Arg64Cys(p.R64C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442738
Start	37956785:37956785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747162109
CDS Mutation	c.33C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442738
Start	37956782:37956782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs75033328
CDS Mutation	c.30C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442738
Start	37959371:37959372(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.120dupC
AA Mutation	p.Ser41LeufsTer76(p.S41Lfs*76)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000333418
Start	38026110:38026111(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.367dupC
AA Mutation	p.Thr124HisfsTer17(p.T124Hfs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> POLR2F

No Mutation Annotation!