Colon Cancer: Gene >> FDXR

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000293195
Start	74864930:74864930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611G>T
AA Mutation	p.Arg204Ile(p.R204I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293195
Start	74864186:74864186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778860222
CDS Mutation	c.964C>T
AA Mutation	p.Arg322Trp(p.R322W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293195
Start	74872062:74872062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.151T>G
AA Mutation	p.Phe51Val(p.F51V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000293195
Start	74872940:74872940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756259973
CDS Mutation	c.5C>T
AA Mutation	p.Ala2Val(p.A2V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000293195
Start	74866836:74866836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218T>C
AA Mutation	p.Val73Ala(p.V73A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293195
Start	74862874:74862874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1419G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293195
Start	74864917:74864917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768414971
CDS Mutation	c.624G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293195
Start	74864538:74864538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545500381
CDS Mutation	c.744G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000293195
Start	74864886:74864886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778482062
CDS Mutation	c.655C>T
AA Mutation	p.Arg219Ter(p.R219*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FDXR

No Mutation Annotation!