Colon Cancer: Gene >> CELF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000290583
Start	151705907:151705907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1185G>T
AA Mutation	p.Glu395Asp(p.E395D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290583
Start	151707165:151707165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746263623
CDS Mutation	c.902A>G
AA Mutation	p.Asn301Ser(p.N301S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290583
Start	151705091:151705091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1348C>T
AA Mutation	p.Arg450Cys(p.R450C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290583
Start	151709018:151709018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466C>A
AA Mutation	p.His156Asn(p.H156N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000290583
Start	151707163:151707163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779202939
CDS Mutation	c.904G>A
AA Mutation	p.Gly302Arg(p.G302R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290583
Start	151706249:151706249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1101G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290583
Start	151709073:151709073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778927541
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290583
Start	151706270:151706270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1080G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290583
Start	151706724:151706724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290583
Start	151705927:151705927(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1165delC
AA Mutation	p.Gln389ArgfsTer38(p.Q389Rfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000290583
Start	151707887:151707887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.535C>T
AA Mutation	p.Arg179Ter(p.R179*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CELF3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290583
Start	151709266:151709266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360C>A
Mutation Classification	Silent
Feature Type	Transcript