Colon Cancer: Gene >> CSNK1E

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359867
Start	38303167:38303167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.158G>T
AA Mutation	p.Ser53Ile(p.S53I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359867
Start	38294230:38294230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097C>T
AA Mutation	p.Ala366Val(p.A366V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359867
Start	38294483:38294483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752107236
CDS Mutation	c.937C>T
AA Mutation	p.Arg313Cys(p.R313C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359867
Start	38299951:38299951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.680G>A
AA Mutation	p.Arg227Gln(p.R227Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359867
Start	38300910:38300910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379C>T
AA Mutation	p.Arg127Trp(p.R127W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359867
Start	38294224:38294224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749796700
CDS Mutation	c.1103C>T
AA Mutation	p.Ser368Leu(p.S368L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359867
Start	38300811:38300811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.478C>A
AA Mutation	p.Arg160Ser(p.R160S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359867
Start	38298872:38298872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.799T>G
AA Mutation	p.Ser267Ala(p.S267A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359867
Start	38294225:38294225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1102T>C
AA Mutation	p.Ser368Pro(p.S368P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359867
Start	38302941:38302941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256G>T
AA Mutation	p.Gly86Trp(p.G86W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359867
Start	38300904:38300904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.385G>A
AA Mutation	p.Val129Ile(p.V129I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359867
Start	38299920:38299920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774242774
CDS Mutation	c.711C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359867
Start	38298923:38298923(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.748delA
AA Mutation	p.Thr250HisfsTer44(p.T250Hfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CSNK1E

No Mutation Annotation!