Colon Cancer: Gene >> TTLL12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43172485:43172485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1411A>G
AA Mutation	p.Ile471Val(p.I471V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43183121:43183121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206T>C
AA Mutation	p.Ile69Thr(p.I69T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43180887:43180887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.401A>G
AA Mutation	p.Gln134Arg(p.Q134R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43174242:43174242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196A>G
AA Mutation	p.Gln399Arg(p.Q399R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43180933:43180933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745511521
CDS Mutation	c.355C>T
AA Mutation	p.Leu119Phe(p.L119F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43180803:43180803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.485C>T
AA Mutation	p.Ala162Val(p.A162V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43180896:43180896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771565831
CDS Mutation	c.392C>T
AA Mutation	p.Ala131Val(p.A131V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43180858:43180858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430C>T
AA Mutation	p.Arg144Cys(p.R144C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43179948:43179948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148175933
CDS Mutation	c.599G>A
AA Mutation	p.Arg200Gln(p.R200Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43180767:43180767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521A>G
AA Mutation	p.Asn174Ser(p.N174S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43169510:43169510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138428335
CDS Mutation	c.1634C>T
AA Mutation	p.Thr545Met(p.T545M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43179963:43179963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584A>G
AA Mutation	p.Asp195Gly(p.D195G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43172407:43172407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1489A>G
AA Mutation	p.Asn497Asp(p.N497D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216129
Start	43179947:43179947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216129
Start	43174379:43174379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768212577
CDS Mutation	c.1059C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216129
Start	43168841:43168841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781032496
CDS Mutation	c.1716C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216129
Start	43179980:43179980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139884471
CDS Mutation	c.567G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216129
Start	43183141:43183141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216129
Start	43174606:43174606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778999708
CDS Mutation	c.927G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000216129
Start	43168145:43168145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755655409
CDS Mutation	c.1798C>T
AA Mutation	p.Gln600Ter(p.Q600*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TTLL12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216129
Start	43174378:43174378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746660164
CDS Mutation	c.1060G>A
AA Mutation	p.Val354Met(p.V354M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript