Colon Cancer: Gene >> GOLGA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128258117:128258117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2290C>T
AA Mutation	p.Arg764Cys(p.R764C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128257638:128257638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2600A>G
AA Mutation	p.Tyr867Cys(p.Y867C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128267513:128267513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201848352
CDS Mutation	c.425C>T
AA Mutation	p.Ala142Val(p.A142V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128273917:128273917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.140A>G
AA Mutation	p.Lys47Arg(p.K47R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128257383:128257383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201662917
CDS Mutation	c.2780C>T
AA Mutation	p.Ala927Val(p.A927V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128260581:128260581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1561C>T
AA Mutation	p.Arg521Cys(p.R521C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128260141:128260141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1726G>A
AA Mutation	p.Val576Ile(p.V576I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128257174:128257174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2902C>T
AA Mutation	p.Arg968Cys(p.R968C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128259279:128259279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1904T>C
AA Mutation	p.Val635Ala(p.V635A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128257205:128257205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2871C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128260112:128260112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757910820
CDS Mutation	c.1755C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128268468:128268468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368496788
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128262650:128262650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128267482:128267482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750162676
CDS Mutation	c.456G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128273895:128273895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.162T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128261511:128261511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1194G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128260507:128260507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1635C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421699
Start	128257111:128257111(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763679060
CDS Mutation	c.2965delT
AA Mutation	p.Tyr989ThrfsTer9(p.Y989Tfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000421699
Start	128257110:128257111(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2965dupT
AA Mutation	p.Tyr989LeufsTer4(p.Y989Lfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000421699
Start	128265594:128265596(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.841_843delAAG
AA Mutation	p.Lys281del(p.K281del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GOLGA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128257108:128257108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2968C>T
AA Mutation	p.Arg990Trp(p.R990W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000421699
Start	128262677:128262677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.939G>T
AA Mutation	p.Glu313Asp(p.E313D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000421699
Start	128273946:128273946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript