Colon Cancer: Gene >> TGIF2LX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283891
Start	89922404:89922404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.319C>T
AA Mutation	p.Arg107Cys(p.R107C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283891
Start	89922519:89922519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434A>G
AA Mutation	p.Lys145Arg(p.K145R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000283891
Start	89922667:89922667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582G>T
AA Mutation	p.Lys194Asn(p.K194N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000283891
Start	89922590:89922590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505A>G
AA Mutation	p.Arg169Gly(p.R169G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000283891
Start	89922099:89922099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773985382
CDS Mutation	c.14C>T
AA Mutation	p.Ala5Val(p.A5V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000283891
Start	89922170:89922170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85G>T
AA Mutation	p.Asp29Tyr(p.D29Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000283891
Start	89922410:89922410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325C>A
AA Mutation	p.Leu109Ile(p.L109I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000283891
Start	89922440:89922440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Asp119Asn(p.D119N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000283891
Start	89922712:89922712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.627G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TGIF2LX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000283891
Start	89922189:89922189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.104G>T
AA Mutation	p.Arg35Ile(p.R35I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000283891
Start	89922519:89922519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434A>C
AA Mutation	p.Lys145Thr(p.K145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript