Colon Cancer: Gene >> TTLL8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000433387
Start	50045949:50045949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367707905
CDS Mutation	c.523C>T
AA Mutation	p.Arg175Trp(p.R175W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000433387
Start	50032108:50032108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747581157
CDS Mutation	c.1333G>A
AA Mutation	p.Ala445Thr(p.A445T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000433387
Start	50045381:50045381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748454999
CDS Mutation	c.625C>T
AA Mutation	p.Arg209Trp(p.R209W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000433387
Start	50050223:50050223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190576024
CDS Mutation	c.184G>A
AA Mutation	p.Gly62Arg(p.G62R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000433387
Start	50016556:50016556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2258G>A
AA Mutation	p.Gly753Asp(p.G753D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000433387
Start	50041625:50041625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146846158
CDS Mutation	c.934G>A
AA Mutation	p.Val312Ile(p.V312I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000433387
Start	50041630:50041630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751926511
CDS Mutation	c.929C>T
AA Mutation	p.Ser310Phe(p.S310F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000433387
Start	50050199:50050199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201087187
CDS Mutation	c.208G>A
AA Mutation	p.Ala70Thr(p.A70T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000433387
Start	50031981:50031981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532527623
CDS Mutation	c.1460G>A
AA Mutation	p.Arg487His(p.R487H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000433387
Start	50045310:50045310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763006164
CDS Mutation	c.696C>A
AA Mutation	p.Ser232Arg(p.S232R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000433387
Start	50032053:50032053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1388G>T
AA Mutation	p.Arg463Leu(p.R463L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000433387
Start	50030727:50030727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1954C>T
AA Mutation	p.Arg652Trp(p.R652W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TTLL8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000433387
Start	50033418:50033418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1115A>G
AA Mutation	p.Glu372Gly(p.E372G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433387
Start	50033348:50033348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758608796
CDS Mutation	c.1185C>T
Mutation Classification	Silent
Feature Type	Transcript