Colon Cancer: Gene >> CELF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11329024:11329024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1498C>T
AA Mutation	p.Arg500Cys(p.R500C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11288448:11288448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851C>T
AA Mutation	p.Ala284Val(p.A284V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11288493:11288493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896G>T
AA Mutation	p.Ser299Ile(p.S299I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11165622:11165622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190G>A
AA Mutation	p.Gly64Arg(p.G64R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11165524:11165524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92A>G
AA Mutation	p.His31Arg(p.H31R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11266631:11266631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.551T>C
AA Mutation	p.Met184Thr(p.M184T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11328983:11328983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1457G>A
AA Mutation	p.Gly486Asp(p.G486D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000416382
Start	11005419:11005419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.32G>T
AA Mutation	p.Arg11Ile(p.R11I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416382
Start	11329035:11329035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539435223
CDS Mutation	c.1509C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416382
Start	11321316:11321316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371442396
CDS Mutation	c.1185C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000416382
Start	11314152:11314152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000416382
Start	11325842:11325843(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1267dupG
AA Mutation	p.Ala423GlyfsTer31(p.A423Gfs*31)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000416382
Start	11328983:11328984(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1457_1458insA
AA Mutation	p.Phe487LeufsTer69(p.F487Lfs*69)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CELF2

No Mutation Annotation!