Colon Cancer: Gene >> TINAGL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271064
Start	31584999:31584999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820C>T
AA Mutation	p.Arg274Cys(p.R274C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271064
Start	31586893:31586893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1318G>A
AA Mutation	p.Val440Met(p.V440M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000271064
Start	31586745:31586745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1253T>C
AA Mutation	p.Leu418Pro(p.L418P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000271064
Start	31585021:31585021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.842T>C
AA Mutation	p.Phe281Ser(p.F281S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000271064
Start	31585210:31585210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.917C>T
AA Mutation	p.Ala306Val(p.A306V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271064
Start	31583494:31583494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.501C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271064
Start	31584938:31584938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759564811
CDS Mutation	c.759C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271064
Start	31577445:31577445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.297T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TINAGL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271064
Start	31577320:31577320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172C>G
AA Mutation	p.Arg58Gly(p.R58G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271064
Start	31584940:31584940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.761T>C
AA Mutation	p.Leu254Pro(p.L254P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript