Colon Cancer: Gene >> EEF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309311
Start	3978067:3978067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1819C>T
AA Mutation	p.Arg607Trp(p.R607W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309311
Start	3983160:3983160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350C>T
AA Mutation	p.Ala117Val(p.A117V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000309311
Start	3984136:3984136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218C>T
AA Mutation	p.Thr73Ile(p.T73I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309311
Start	3979942:3979942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1471G>A
AA Mutation	p.Ala491Thr(p.A491T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309311
Start	3984250:3984250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104T>C
AA Mutation	p.Leu35Pro(p.L35P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000309311
Start	3979992:3979992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1421G>A
AA Mutation	p.Gly474Asp(p.G474D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000309311
Start	3983211:3983211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299T>G
AA Mutation	p.Ile100Ser(p.I100S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000309311
Start	3981984:3981984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767351133
CDS Mutation	c.860G>A
AA Mutation	p.Arg287His(p.R287H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309311
Start	3982034:3982034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201754413
CDS Mutation	c.810C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309311
Start	3977918:3977918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769162318
CDS Mutation	c.1968C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309311
Start	3976698:3976698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2433G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309311
Start	3982316:3982316(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.721delG
AA Mutation	p.Glu241ArgfsTer13(p.E241Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> EEF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309311
Start	3982285:3982285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.752A>C
AA Mutation	p.Lys251Thr(p.K251T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript