Colon Cancer: Gene >> EIF2AK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000199389
Start	6037494:6037494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1262A>C
AA Mutation	p.Lys421Thr(p.K421T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000199389
Start	6047029:6047029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765245380
CDS Mutation	c.512C>T
AA Mutation	p.Ala171Val(p.A171V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000199389
Start	6042949:6042949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.775G>A
AA Mutation	p.Asp259Asn(p.D259N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000199389
Start	6037434:6037434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322G>A
AA Mutation	p.Arg441Gln(p.R441Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000199389
Start	6054647:6054647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.176T>C
AA Mutation	p.Phe59Ser(p.F59S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000199389
Start	6049956:6049956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.367G>C
AA Mutation	p.Ala123Pro(p.A123P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000199389
Start	6026838:6026838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1654A>T
AA Mutation	p.Arg552Trp(p.R552W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000199389
Start	6044597:6044597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771599948
CDS Mutation	c.695C>T
AA Mutation	p.Ala232Val(p.A232V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000199389
Start	6026894:6026894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1598G>A
AA Mutation	p.Arg533Gln(p.R533Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000199389
Start	6024767:6024767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1799A>C
AA Mutation	p.Gln600Pro(p.Q600P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000199389
Start	6049957:6049957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.366A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000199389
Start	6046109:6046109(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.592delA
AA Mutation	p.Ile198SerfsTer2(p.I198Sfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000199389
Start	6041068:6041068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.943G>T
AA Mutation	p.Glu315Ter(p.E315*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000199389
Start	6044565:6044565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727C>T
AA Mutation	p.Arg243Ter(p.R243*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000199389
Start	6026895:6026895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754214883
CDS Mutation	c.1597C>T
AA Mutation	p.Arg533Ter(p.R533*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000199389
Start	6042940:6042940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784G>T
AA Mutation	p.Glu262Ter(p.E262*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000199389
Start	6046130:6046130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571C>T
AA Mutation	p.Gln191Ter(p.Q191*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EIF2AK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000199389
Start	6037434:6037434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322G>A
AA Mutation	p.Arg441Gln(p.R441Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript