Colon Cancer: Gene >> IRAK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256458
Start	10200432:10200432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.341A>C
AA Mutation	p.Lys114Thr(p.K114T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256458
Start	10222760:10222760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1138G>A
AA Mutation	p.Ala380Thr(p.A380T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256458
Start	10219710:10219710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139476001
CDS Mutation	c.934C>T
AA Mutation	p.Arg312Cys(p.R312C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256458
Start	10200433:10200433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.342G>C
AA Mutation	p.Lys114Asn(p.K114N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256458
Start	10222797:10222797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1175T>G
AA Mutation	p.Leu392Arg(p.L392R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000256458
Start	10209666:10209666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141312230
CDS Mutation	c.502G>A
AA Mutation	p.Asp168Asn(p.D168N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000256458
Start	10238893:10238893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1619C>T
AA Mutation	p.Ser540Phe(p.S540F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000256458
Start	10238887:10238887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1613A>T
AA Mutation	p.Asp538Val(p.D538V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000256458
Start	10213515:10213515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755G>T
AA Mutation	p.Arg252Ile(p.R252I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256458
Start	10178013:10178013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256458
Start	10242129:10242129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372211228
CDS Mutation	c.1779G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256458
Start	10216943:10216943(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.801delC
AA Mutation	p.Asn268MetfsTer102(p.N268Mfs*102)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256458
Start	10222789:10222789(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1170delG
AA Mutation	p.Gln391SerfsTer2(p.Q391Sfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IRAK2

No Mutation Annotation!