Colon Cancer: Gene >> IFT81

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242591
Start	110129095:110129095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394C>A
AA Mutation	p.Leu132Ile(p.L132I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242591
Start	110203907:110203907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1601G>T
AA Mutation	p.Ser534Ile(p.S534I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242591
Start	110205616:110205616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs527626533
CDS Mutation	c.1738C>T
AA Mutation	p.Arg580Cys(p.R580C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242591
Start	110127454:110127454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.74C>T
AA Mutation	p.Thr25Met(p.T25M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000242591
Start	110127492:110127492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112C>T
AA Mutation	p.Leu38Phe(p.L38F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000242591
Start	110163045:110163045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1168G>A
AA Mutation	p.Glu390Lys(p.E390K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242591
Start	110143410:110143410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.810A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242591
Start	110203914:110203914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1608A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242591
Start	110180508:110180508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763039671
CDS Mutation	c.1275C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000242591
Start	110180428:110180428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374954469
CDS Mutation	c.1195C>T
AA Mutation	p.Arg399Ter(p.R399*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242591
Start	110129060:110129061(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs756551252
CDS Mutation	c.365dupT
AA Mutation	p.Leu122PhefsTer5(p.L122Ffs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242591
Start	110192619:110192620(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1476dupA
AA Mutation	p.Leu493ThrfsTer7(p.L493Tfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IFT81

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242591
Start	110205613:110205613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760804753
CDS Mutation	c.1735C>T
AA Mutation	p.Arg579Cys(p.R579C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript