Colon Cancer: Gene >> CELF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37274397:37274397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.715C>T
AA Mutation	p.Arg239Trp(p.R239W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37270782:37270782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1085T>C
AA Mutation	p.Ile362Thr(p.I362T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37270867:37270867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751100448
CDS Mutation	c.1000T>C
AA Mutation	p.Ser334Pro(p.S334P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37274406:37274406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.706C>T
AA Mutation	p.Arg236Cys(p.R236C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37273084:37273084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881C>T
AA Mutation	p.Ala294Val(p.A294V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37274393:37274393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.719G>A
AA Mutation	p.Arg240Gln(p.R240Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37270854:37270854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1013T>C
AA Mutation	p.Val338Ala(p.V338A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37273042:37273042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372830155
CDS Mutation	c.923C>T
AA Mutation	p.Ala308Val(p.A308V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37274405:37274405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.707G>A
AA Mutation	p.Arg236His(p.R236H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37321818:37321818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148456424
CDS Mutation	c.433C>T
AA Mutation	p.Arg145Cys(p.R145C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420428
Start	37275176:37275176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420428
Start	37565420:37565420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420428
Start	37273131:37273131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420428
Start	37565366:37565366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420428
Start	37253817:37253817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1455G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420428
Start	37274446:37274446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778279875
CDS Mutation	c.666G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000420428
Start	37565579:37565579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.63C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000420428
Start	37270830:37270830(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1037delC
AA Mutation	p.Pro346HisfsTer54(p.P346Hfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000420428
Start	37264689:37264689(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1234delC
AA Mutation	p.Gln412SerfsTer26(p.Q412Sfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CELF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37274844:37274844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.618G>T
AA Mutation	p.Gln206His(p.Q206H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37565430:37565430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.212A>G
AA Mutation	p.Lys71Arg(p.K71R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000420428
Start	37565437:37565437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.205G>T
AA Mutation	p.Asp69Tyr(p.D69Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript