Colon Cancer: Gene >> TBC1D9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140622706:140622706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3290C>T
AA Mutation	p.Pro1097Leu(p.P1097L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140627478:140627478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2862G>C
AA Mutation	p.Gln954His(p.Q954H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140634101:140634101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757180833
CDS Mutation	c.2593C>T
AA Mutation	p.Arg865Cys(p.R865C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140659605:140659605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1904A>G
AA Mutation	p.Tyr635Cys(p.Y635C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140634100:140634100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753790959
CDS Mutation	c.2594G>A
AA Mutation	p.Arg865His(p.R865H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140634146:140634146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563665831
CDS Mutation	c.2548G>A
AA Mutation	p.Ala850Thr(p.A850T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140634119:140634119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2575C>T
AA Mutation	p.Pro859Ser(p.P859S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140622742:140622742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3254C>T
AA Mutation	p.Pro1085Leu(p.P1085L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140701549:140701549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.196T>A
AA Mutation	p.Leu66Met(p.L66M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140756015:140756015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.31G>A
AA Mutation	p.Ala11Thr(p.A11T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140657189:140657189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2245C>T
AA Mutation	p.Pro749Ser(p.P749S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000442267
Start	140678943:140678943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850C>T
AA Mutation	p.Arg284Cys(p.R284C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140668944:140668944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1561C>T
AA Mutation	p.Arg521Cys(p.R521C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140670890:140670890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096C>T
AA Mutation	p.Leu366Phe(p.L366F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140639367:140639367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2399T>G
AA Mutation	p.Val800Gly(p.V800G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140639368:140639368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2398G>T
AA Mutation	p.Val800Leu(p.V800L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140661969:140661969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1727A>G
AA Mutation	p.Asn576Ser(p.N576S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140701562:140701562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140668996:140668996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1509C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140676903:140676903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376544697
CDS Mutation	c.1050G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140669706:140669706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751576434
CDS Mutation	c.1365C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140657711:140657711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2023C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140634159:140634159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376886163
CDS Mutation	c.2535C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140686359:140686359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.345G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140670795:140670795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1191T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140627448:140627448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2892T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442267
Start	140622366:140622366(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3630delC
AA Mutation	p.Ile1211SerfsTer11(p.I1211Sfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000442267
Start	140677033:140677033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920T>G
AA Mutation	p.Leu307Ter(p.L307*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442267
Start	140678958:140678959(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.834dupA
AA Mutation	p.Val279SerfsTer7(p.V279Sfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442267
Start	140622261:140622262(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3734dupA
AA Mutation	p.Asn1245LysfsTer14(p.N1245Kfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TBC1D9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140679743:140679743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461T>C
AA Mutation	p.Met154Thr(p.M154T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140669732:140669732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781475633
CDS Mutation	c.1339C>T
AA Mutation	p.Arg447Cys(p.R447C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140622377:140622377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754331118
CDS Mutation	c.3619C>T
AA Mutation	p.Arg1207Trp(p.R1207W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140657686:140657686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2048T>A
AA Mutation	p.Leu683His(p.L683H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140634067:140634067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375019047
CDS Mutation	c.2627C>T
AA Mutation	p.Ala876Val(p.A876V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140657190:140657190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2244G>C
Mutation Classification	Silent
Feature Type	Transcript