Colon Cancer: Gene >> IRAK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000551736
Start	43768234:43768234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123A>C
AA Mutation	p.Lys41Asn(p.K41N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000551736
Start	43772950:43772950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141209982
CDS Mutation	c.529A>G
AA Mutation	p.Thr177Ala(p.T177A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000551736
Start	43782441:43782441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1076C>T
AA Mutation	p.Ala359Val(p.A359V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000551736
Start	43782356:43782356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.991G>A
AA Mutation	p.Gly331Ser(p.G331S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000551736
Start	43786434:43786434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1224G>C
AA Mutation	p.Lys408Asn(p.K408N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000551736
Start	43768145:43768145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377584435
CDS Mutation	c.34C>T
AA Mutation	p.Arg12Cys(p.R12C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000551736
Start	43772181:43772181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.309T>G
AA Mutation	p.Asp103Glu(p.D103E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000551736
Start	43782447:43782447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764106350
CDS Mutation	c.1082G>A
AA Mutation	p.Arg361His(p.R361H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551736
Start	43768234:43768234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551138584
CDS Mutation	c.123A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551736
Start	43768240:43768240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000551736
Start	43777720:43777720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.807A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000551736
Start	43771247:43771247(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.193delA
AA Mutation	p.Ser65ValfsTer24(p.S65Vfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IRAK4

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000551736
Start	43782309:43782309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.944C>A
AA Mutation	p.Ala315Glu(p.A315E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript