Colon Cancer: Gene >> TGS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260129
Start	55786731:55786731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833A>G
AA Mutation	p.Glu278Gly(p.E278G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260129
Start	55813049:55813049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2370T>G
AA Mutation	p.Ile790Met(p.I790M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260129
Start	55796006:55796006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547391666
CDS Mutation	c.1396C>T
AA Mutation	p.Arg466Trp(p.R466W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260129
Start	55796022:55796022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1412T>C
AA Mutation	p.Leu471Ser(p.L471S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260129
Start	55798923:55798923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1552T>A
AA Mutation	p.Phe518Ile(p.F518I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260129
Start	55824585:55824585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2444C>T
AA Mutation	p.Ala815Val(p.A815V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260129
Start	55805012:55805012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2119C>G
AA Mutation	p.Gln707Glu(p.Q707E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000260129
Start	55795996:55795996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1386T>G
AA Mutation	p.Asn462Lys(p.N462K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260129
Start	55802476:55802476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1869G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000260129
Start	55824680:55824680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2539C>T
AA Mutation	p.Arg847Ter(p.R847*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260129
Start	55799039:55799040(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1674dupA
AA Mutation	p.Gly559ArgfsTer2(p.G559Rfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TGS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260129
Start	55773658:55773658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.40C>A
AA Mutation	p.Leu14Ile(p.L14I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260129
Start	55786911:55786911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013C>T
AA Mutation	p.Ser338Phe(p.S338F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260129
Start	55813092:55813092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2413C>A
AA Mutation	p.Leu805Ile(p.L805I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260129
Start	55799133:55799133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1762G>A
AA Mutation	p.Glu588Lys(p.E588K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript