Colon Cancer: Gene >> TUFM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313511
Start	28844023:28844023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753682714
CDS Mutation	c.1001G>A
AA Mutation	p.Arg334Gln(p.R334Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313511
Start	28844331:28844331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821G>A
AA Mutation	p.Arg274His(p.R274H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313511
Start	28844053:28844053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971A>G
AA Mutation	p.Asn324Ser(p.N324S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313511
Start	28843755:28843755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1175T>A
AA Mutation	p.Ile392Asn(p.I392N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000313511
Start	28845475:28845475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253G>A
AA Mutation	p.Ala85Thr(p.A85T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000313511
Start	28844302:28844302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.850C>A
AA Mutation	p.Arg284Ser(p.R284S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000313511
Start	28845963:28845963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.196A>G
AA Mutation	p.Ile66Val(p.I66V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000313511
Start	28844302:28844302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs180768366
CDS Mutation	c.850C>T
AA Mutation	p.Arg284Cys(p.R284C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313511
Start	28844067:28844067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778365709
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313511
Start	28844004:28844004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000313511
Start	28843061:28843061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1282C>T
AA Mutation	p.Arg428Ter(p.R428*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TUFM

No Mutation Annotation!