Colon Cancer: Gene >> TLR10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308973
Start	38774762:38774762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829C>G
AA Mutation	p.Arg277Gly(p.R277G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308973
Start	38773781:38773781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1810C>T
AA Mutation	p.Pro604Ser(p.P604S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308973
Start	38773315:38773315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2276A>C
AA Mutation	p.Lys759Thr(p.K759T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308973
Start	38774212:38774212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1379A>C
AA Mutation	p.Lys460Thr(p.K460T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308973
Start	38774182:38774182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1409A>G
AA Mutation	p.Glu470Gly(p.E470G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308973
Start	38775439:38775439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375480992
CDS Mutation	c.152C>T
AA Mutation	p.Thr51Met(p.T51M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308973
Start	38774275:38774275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1316G>T
AA Mutation	p.Arg439Met(p.R439M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308973
Start	38773581:38773581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2010C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308973
Start	38773335:38773335(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2256delA
AA Mutation	p.Ala753HisfsTer28(p.A753Hfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000308973
Start	38774183:38774183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1408G>T
AA Mutation	p.Glu470Ter(p.E470*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308973
Start	38775557:38775558(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.33_34insTATAGGATAAATCC
AA Mutation	p.Ser12TyrfsTer9(p.S12Yfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TLR10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308973
Start	38773657:38773657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1934C>T
AA Mutation	p.Ser645Phe(p.S645F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308973
Start	38774035:38774035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149319935
CDS Mutation	c.1556C>T
AA Mutation	p.Ala519Val(p.A519V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308973
Start	38773386:38773386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2205C>A
AA Mutation	p.Phe735Leu(p.F735L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308973
Start	38775326:38775326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265C>T
AA Mutation	p.Leu89Phe(p.L89F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308973
Start	38775577:38775577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.14G>T
AA Mutation	p.Arg5Ile(p.R5I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308973
Start	38773665:38773665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1926A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308973
Start	38773695:38773695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148341393
CDS Mutation	c.1896C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308973
Start	38773407:38773407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2184C>A
Mutation Classification	Silent
Feature Type	Transcript