Colon Cancer: Gene >> TLR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38798506:38798506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326C>A
AA Mutation	p.Ser109Tyr(p.S109Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38797867:38797867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.965T>G
AA Mutation	p.Ile322Ser(p.I322S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38798053:38798053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779C>A
AA Mutation	p.Ser260Tyr(p.S260Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38797232:38797232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1600G>A
AA Mutation	p.Glu534Lys(p.E534K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38797073:38797073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370009768
CDS Mutation	c.1759G>A
AA Mutation	p.Val587Ile(p.V587I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38798179:38798179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.653T>G
AA Mutation	p.Leu218Arg(p.L218R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38796784:38796784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2048T>C
AA Mutation	p.Ile683Thr(p.I683T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38798821:38798821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.11T>C
AA Mutation	p.Ile4Thr(p.I4T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38797861:38797861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143619350
CDS Mutation	c.971C>T
AA Mutation	p.Ser324Leu(p.S324L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38798749:38798749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.83T>C
AA Mutation	p.Leu28Ser(p.L28S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308979
Start	38797467:38797467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748741180
CDS Mutation	c.1365T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308979
Start	38798363:38798363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308979
Start	38797761:38797761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1071T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308979
Start	38798622:38798622(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.210delA
AA Mutation	p.Lys70AsnfsTer2(p.K70Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TLR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38796665:38796665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2167T>G
AA Mutation	p.Ser723Ala(p.S723A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38796574:38796574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2258G>T
AA Mutation	p.Arg753Met(p.R753M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38796893:38796893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751096819
CDS Mutation	c.1939G>A
AA Mutation	p.Asp647Asn(p.D647N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38797396:38797396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436C>A
AA Mutation	p.Ser479Tyr(p.S479Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308979
Start	38798087:38798087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745C>A
AA Mutation	p.Leu249Ile(p.L249I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308979
Start	38797860:38797860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140075350
CDS Mutation	c.972G>A
Mutation Classification	Silent
Feature Type	Transcript