Colon Cancer: Gene >> EIF4G1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184327338:184327338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756664955
CDS Mutation	c.3551G>A
AA Mutation	p.Arg1184Gln(p.R1184Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184321519:184321519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754009820
CDS Mutation	c.935G>A
AA Mutation	p.Arg312His(p.R312H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184320693:184320693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601C>T
AA Mutation	p.Arg201Cys(p.R201C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184326569:184326569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3265G>T
AA Mutation	p.Gly1089Trp(p.G1089W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000346169
Start	184323409:184323409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2090C>T
AA Mutation	p.Ala697Val(p.A697V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184315815:184315815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19T>C
AA Mutation	p.Ser7Pro(p.S7P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184328711:184328711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4034C>T
AA Mutation	p.Thr1345Ile(p.T1345I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184327365:184327365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3578G>A
AA Mutation	p.Arg1193Gln(p.R1193Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184316205:184316205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.134C>A
AA Mutation	p.Ser45Tyr(p.S45Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184320964:184320964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752416317
CDS Mutation	c.668C>T
AA Mutation	p.Thr223Met(p.T223M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184319793:184319793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Cys(p.R177C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184320694:184320694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34838305
CDS Mutation	c.602G>A
AA Mutation	p.Arg201His(p.R201H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184321749:184321749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165G>A
AA Mutation	p.Glu389Lys(p.E389K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184327845:184327845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3796G>A
AA Mutation	p.Val1266Met(p.V1266M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000346169
Start	184319800:184319800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536C>T
AA Mutation	p.Thr179Met(p.T179M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184324935:184324935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2677C>T
AA Mutation	p.Arg893Trp(p.R893W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346169
Start	184331346:184331346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4242T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346169
Start	184321367:184321367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374764057
CDS Mutation	c.783G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346169
Start	184321970:184321970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779808419
CDS Mutation	c.1386A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346169
Start	184334749:184334749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149243787
CDS Mutation	c.4641C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346169
Start	184327847:184327847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3798G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346169
Start	184327907:184327907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748359022
CDS Mutation	c.3858G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346169
Start	184331992:184331992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112264710
CDS Mutation	c.4524G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346169
Start	184327606:184327606(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3686delC
AA Mutation	p.Pro1229GlnfsTer2(p.P1229Qfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346169
Start	184321883:184321884(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1305dupC
AA Mutation	p.Thr436HisfsTer40(p.T436Hfs*40)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000346169
Start	184327214:184327214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3429-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> EIF4G1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184323870:184323870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2365G>A
AA Mutation	p.Asp789Asn(p.D789N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184323946:184323946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2441C>T
AA Mutation	p.Ala814Val(p.A814V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184321787:184321787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1203G>T
AA Mutation	p.Glu401Asp(p.E401D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184323469:184323469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2150C>A
AA Mutation	p.Ala717Asp(p.A717D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000346169
Start	184325091:184325091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2833G>T
AA Mutation	p.Asp945Tyr(p.D945Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346169
Start	184326598:184326598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346169
Start	184326619:184326619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3315C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346169
Start	184317455:184317455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.282C>A
Mutation Classification	Silent
Feature Type	Transcript