Colon Cancer: Gene >> TTC12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000529221
Start	113339405:113339405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.757T>C
AA Mutation	p.Ser253Pro(p.S253P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000529221
Start	113352200:113352200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1439G>T
AA Mutation	p.Ser480Ile(p.S480I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000529221
Start	113338808:113338808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.611A>G
AA Mutation	p.Asn204Ser(p.N204S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000529221
Start	113335017:113335017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556G>A
AA Mutation	p.Ala186Thr(p.A186T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000529221
Start	113323417:113323417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.188A>C
AA Mutation	p.Lys63Thr(p.K63T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000529221
Start	113352119:113352119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1358C>T
AA Mutation	p.Ala453Val(p.A453V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000529221
Start	113324677:113324677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145843861
CDS Mutation	c.317C>T
AA Mutation	p.Ala106Val(p.A106V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000529221
Start	113323424:113323424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195G>A
AA Mutation	p.Met65Ile(p.M65I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000529221
Start	113325583:113325583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372770355
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Cys(p.R128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529221
Start	113335013:113335013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529221
Start	113340719:113340719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782138110
CDS Mutation	c.882C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529221
Start	113329958:113329958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529221
Start	113329958:113329958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.483G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529221
Start	113340707:113340707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000529221
Start	113339313:113339313(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.669delA
AA Mutation	p.Ala224GlnfsTer20(p.A224Qfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000529221
Start	113339438:113339438(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.795delG
AA Mutation	p.Ile266LeufsTer4(p.I266Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TTC12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000529221
Start	113359430:113359430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1514A>G
AA Mutation	p.Asn505Ser(p.N505S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000529221
Start	113364937:113364937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1919C>A
AA Mutation	p.Ser640Tyr(p.S640Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529221
Start	113335013:113335013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000529221
Start	113341921:113341921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.981G>A
Mutation Classification	Silent
Feature Type	Transcript