Colon Cancer: Gene >> TLR5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223111513:223111513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1519C>A
AA Mutation	p.Leu507Met(p.L507M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223111619:223111619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1413G>T
AA Mutation	p.Glu471Asp(p.E471D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223112355:223112355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.677T>C
AA Mutation	p.Met226Thr(p.M226T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223112586:223112586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372708351
CDS Mutation	c.446G>A
AA Mutation	p.Arg149His(p.R149H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223112970:223112970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62T>G
AA Mutation	p.Ile21Ser(p.I21S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223111971:223111971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139394912
CDS Mutation	c.1061C>T
AA Mutation	p.Ser354Leu(p.S354L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223110825:223110825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2207C>G
AA Mutation	p.Pro736Arg(p.P736R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366881
Start	223112276:223112276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366881
Start	223111988:223111988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366881
Start	223112441:223112441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000366881
Start	223112429:223112429(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.603delT
AA Mutation	p.Phe201LeufsTer20(p.F201Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000366881
Start	223112947:223112947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200942023
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Ter(p.R29*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TLR5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223110850:223110850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2182T>C
AA Mutation	p.Cys728Arg(p.C728R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223110528:223110528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2504A>C
AA Mutation	p.Gln835Pro(p.Q835P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223111720:223111720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1312C>A
AA Mutation	p.Leu438Ile(p.L438I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223110925:223110925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2107G>T
AA Mutation	p.Asp703Tyr(p.D703Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223111925:223111925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1107G>T
AA Mutation	p.Lys369Asn(p.K369N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000366881
Start	223112648:223112648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384C>A
AA Mutation	p.Phe128Leu(p.F128L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366881
Start	223112231:223112231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200513847
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366881
Start	223112462:223112462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758596845
CDS Mutation	c.570C>T
Mutation Classification	Silent
Feature Type	Transcript