Colon Cancer: Gene >> RNF41

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345093
Start	56210538:56210538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.121G>A
AA Mutation	p.Ala41Thr(p.A41T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345093
Start	56207661:56207661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587A>G
AA Mutation	p.Tyr196Cys(p.Y196C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345093
Start	56210442:56210442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.217C>T
AA Mutation	p.Arg73Trp(p.R73W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345093
Start	56206776:56206776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625G>A
AA Mutation	p.Ala209Thr(p.A209T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345093
Start	56206656:56206656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745A>G
AA Mutation	p.Asn249Asp(p.N249D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000345093
Start	56210297:56210297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362G>A
AA Mutation	p.Gly121Asp(p.G121D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345093
Start	56206525:56206525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.876G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345093
Start	56210512:56210512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000345093
Start	56206531:56206532(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.869_870insT
AA Mutation	p.Cys291LeufsTer2(p.C291Lfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RNF41

No Mutation Annotation!