Colon Cancer: Gene >> MX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398598
Start	41458721:41458721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758038928
CDS Mutation	c.1952C>T
AA Mutation	p.Thr651Met(p.T651M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398598
Start	41440893:41440893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598A>G
AA Mutation	p.Thr200Ala(p.T200A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398598
Start	41458575:41458575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1806C>A
AA Mutation	p.Phe602Leu(p.F602L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398598
Start	41441865:41441865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.880G>A
AA Mutation	p.Glu294Lys(p.E294K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398598
Start	41443828:41443828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.970G>A
AA Mutation	p.Ala324Thr(p.A324T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398598
Start	41452768:41452768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1657G>A
AA Mutation	p.Glu553Lys(p.E553K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398598
Start	41441778:41441778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.793C>T
AA Mutation	p.Arg265Trp(p.R265W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000398598
Start	41440909:41440909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614A>G
AA Mutation	p.Tyr205Cys(p.Y205C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398598
Start	41435953:41435953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200861936
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398598
Start	41441827:41441827(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.845delG
AA Mutation	p.Gly282AlafsTer9(p.G282Afs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398598
Start	41445548:41445548(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776684659
CDS Mutation	c.1114delA
AA Mutation	p.Met372CysfsTer4(p.M372Cfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MX1

No Mutation Annotation!