Colon Cancer: Gene >> EME1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338165
Start	50375498:50375498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290C>T
AA Mutation	p.Ala97Val(p.A97V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338165
Start	50380928:50380928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1702A>G
AA Mutation	p.Ser568Gly(p.S568G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338165
Start	50380893:50380893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1667A>G
AA Mutation	p.Gln556Arg(p.Q556R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338165
Start	50376084:50376084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.794G>A
AA Mutation	p.Gly265Asp(p.G265D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338165
Start	50375586:50375586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377462951
CDS Mutation	c.378A>C
AA Mutation	p.Gln126His(p.Q126H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000338165
Start	50375769:50375769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561A>C
AA Mutation	p.Lys187Asn(p.K187N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000338165
Start	50380484:50380484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1519C>T
AA Mutation	p.Pro507Ser(p.P507S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000338165
Start	50380881:50380881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140304684
CDS Mutation	c.1655G>A
AA Mutation	p.Arg552His(p.R552H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338165
Start	50380342:50380342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1377C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338165
Start	50378627:50378627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.936A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338165
Start	50380373:50380373(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1409delA
AA Mutation	p.Lys470ArgfsTer11(p.K470Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000338165
Start	50375984:50375984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> EME1

No Mutation Annotation!