Colon Cancer: Gene >> TTLL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000426895
Start	9812946:9812946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187487302
CDS Mutation	c.481A>C
AA Mutation	p.Lys161Gln(p.K161Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000426895
Start	9835219:9835219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2478C>A
AA Mutation	p.Asp826Glu(p.D826E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000426895
Start	9813105:9813105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640G>A
AA Mutation	p.Glu214Lys(p.E214K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000426895
Start	9829144:9829144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770396917
CDS Mutation	c.1732G>A
AA Mutation	p.Ala578Thr(p.A578T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000426895
Start	9829361:9829361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1949G>A
AA Mutation	p.Cys650Tyr(p.C650Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000426895
Start	9828986:9828986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1574T>C
AA Mutation	p.Ile525Thr(p.I525T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000426895
Start	9829355:9829355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368192955
CDS Mutation	c.1943G>A
AA Mutation	p.Arg648His(p.R648H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000426895
Start	9820722:9820722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779691492
CDS Mutation	c.1135C>T
AA Mutation	p.Arg379Cys(p.R379C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000426895
Start	9829112:9829112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1700T>C
AA Mutation	p.Ile567Thr(p.I567T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000426895
Start	9835304:9835304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376875827
CDS Mutation	c.2563C>T
AA Mutation	p.Arg855Cys(p.R855C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426895
Start	9827211:9827211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765125832
CDS Mutation	c.1518G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426895
Start	9835162:9835162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767751592
CDS Mutation	c.2421G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426895
Start	9829329:9829329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759555843
CDS Mutation	c.1917C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426895
Start	9835360:9835360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751049382
CDS Mutation	c.2619C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000426895
Start	9833246:9833246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2125+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TTLL3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000426895
Start	9829329:9829329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759555843
CDS Mutation	c.1917C>T
Mutation Classification	Silent
Feature Type	Transcript