Colon Cancer: Gene >> ILF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000590261
Start	10681065:10681065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004G>A
AA Mutation	p.Gly335Asp(p.G335D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000590261
Start	10671026:10671026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.56C>A
AA Mutation	p.Ser19Tyr(p.S19Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000590261
Start	10679161:10679161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.716G>A
AA Mutation	p.Arg239His(p.R239H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000590261
Start	10681297:10681297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1148C>T
AA Mutation	p.Pro383Leu(p.P383L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000590261
Start	10687412:10687412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2126G>A
AA Mutation	p.Gly709Asp(p.G709D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000590261
Start	10681252:10681252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103C>T
AA Mutation	p.Thr368Met(p.T368M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000590261
Start	10683513:10683513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575931762
CDS Mutation	c.1822G>A
AA Mutation	p.Val608Ile(p.V608I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000590261
Start	10682637:10682637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780654204
CDS Mutation	c.1481C>T
AA Mutation	p.Ala494Val(p.A494V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000590261
Start	10682167:10682167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370373655
CDS Mutation	c.1355C>T
AA Mutation	p.Thr452Met(p.T452M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000590261
Start	10679163:10679163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200955896
CDS Mutation	c.718G>A
AA Mutation	p.Val240Met(p.V240M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000590261
Start	10680436:10680436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.950G>A
AA Mutation	p.Ser317Asn(p.S317N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590261
Start	10688653:10688653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2526C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590261
Start	10671120:10671120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590261
Start	10678629:10678629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590261
Start	10689279:10689279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2652C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590261
Start	10671093:10671093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764217068
CDS Mutation	c.123G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590261
Start	10677237:10677237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756744264
CDS Mutation	c.486G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590261
Start	10683939:10683939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2028G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ILF3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000590261
Start	10683789:10683789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2005G>A
AA Mutation	p.Gly669Ser(p.G669S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590261
Start	10677213:10677213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142885843
CDS Mutation	c.462G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000590261
Start	10688656:10688656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2529C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000590261
Start	10683690:10683690(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1911delC
AA Mutation	p.Asn638ThrfsTer29(p.N638Tfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript