Colon Cancer: Gene >> TSC22D1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44574098:44574098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1977G>T
AA Mutation	p.Gln659His(p.Q659H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44574760:44574760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1315A>G
AA Mutation	p.Thr439Ala(p.T439A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44574155:44574155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1920G>A
AA Mutation	p.Met640Ile(p.M640I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44574822:44574822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1253C>T
AA Mutation	p.Pro418Leu(p.P418L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44575656:44575656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419A>C
AA Mutation	p.Asp140Ala(p.D140A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44574424:44574424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779732270
CDS Mutation	c.1651T>C
AA Mutation	p.Ser551Pro(p.S551P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44574554:44574554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1521G>T
AA Mutation	p.Gln507His(p.Q507H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44576019:44576019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.56C>T
AA Mutation	p.Ala19Val(p.A19V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44575195:44575195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779440319
CDS Mutation	c.880C>T
AA Mutation	p.Arg294Cys(p.R294C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44573384:44573384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2691C>A
AA Mutation	p.Phe897Leu(p.F897L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44575093:44575093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760138310
CDS Mutation	c.982G>A
AA Mutation	p.Val328Met(p.V328M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458659
Start	44574068:44574068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781265296
CDS Mutation	c.2007C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458659
Start	44575577:44575577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458659
Start	44573819:44573819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2256A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458659
Start	44575874:44575874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.201G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000458659
Start	44574812:44574812(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1263delA
AA Mutation	p.Gly422ValfsTer22(p.G422Vfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000458659
Start	44434702:44434702(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3146delC
AA Mutation	p.Pro1049LeufsTer38(p.P1049Lfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000458659
Start	44574553:44574553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1522C>T
AA Mutation	p.Gln508Ter(p.Q508*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000458659
Start	44573531:44573532(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2543dupC
AA Mutation	p.Thr849AsnfsTer19(p.T849Nfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000458659
Start	44574821:44574822(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1253_1254insAT
AA Mutation	p.Phe419SerfsTer26(p.F419Sfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TSC22D1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44575209:44575209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.866T>C
AA Mutation	p.Val289Ala(p.V289A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000458659
Start	44574067:44574067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531498658
CDS Mutation	c.2008G>A
AA Mutation	p.Gly670Arg(p.G670R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript