Colon Cancer: Gene >> TLR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713789:117713789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1661A>G
AA Mutation	p.Asn554Ser(p.N554S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117712634:117712634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506A>C
AA Mutation	p.Glu169Ala(p.E169A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713397:117713397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1269A>C
AA Mutation	p.Gln423His(p.Q423H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117714127:117714127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1999T>C
AA Mutation	p.Tyr667His(p.Y667H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713382:117713382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254C>A
AA Mutation	p.Phe418Leu(p.F418L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117712578:117712578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450A>C
AA Mutation	p.Lys150Asn(p.K150N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713563:117713563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435G>A
AA Mutation	p.Ala479Thr(p.A479T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117714140:117714140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2012A>G
AA Mutation	p.Glu671Gly(p.E671G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117714259:117714259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2131G>A
AA Mutation	p.Asp711Asn(p.D711N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117712697:117712697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569T>G
AA Mutation	p.Ile190Ser(p.I190S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117714227:117714227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2099T>C
AA Mutation	p.Val700Ala(p.V700A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355622
Start	117712968:117712968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.840G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355622
Start	117714270:117714270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201667292
CDS Mutation	c.2142C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355622
Start	117714459:117714459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2331C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355622
Start	117713184:117713184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1056T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000355622
Start	117712912:117712912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784G>T
AA Mutation	p.Glu262Ter(p.E262*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TLR4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117714259:117714259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2131G>T
AA Mutation	p.Asp711Tyr(p.D711Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713470:117713470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1342A>C
AA Mutation	p.Asn448His(p.N448H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117713945:117713945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773808914
CDS Mutation	c.1817G>A
AA Mutation	p.Arg606Gln(p.R606Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355622
Start	117712610:117712610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.482T>G
AA Mutation	p.Leu161Arg(p.L161R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000355622
Start	117712801:117712801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673G>T
AA Mutation	p.Glu225Ter(p.E225*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript