Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IRAK3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000261233
Start	66217173:66217173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.591G>T
AA Mutation	p.Glu197Asp(p.E197D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261233
Start	66247960:66247960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1580G>T
AA Mutation	p.Arg527Ile(p.R527I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261233
Start	66228283:66228283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371798024
CDS Mutation	c.800G>A
AA Mutation	p.Arg267Gln(p.R267Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261233
Start	66245210:66245210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1262T>C
AA Mutation	p.Leu421Ser(p.L421S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261233
Start	66203777:66203777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.200G>A
AA Mutation	p.Ser67Asn(p.S67N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261233
Start	66217174:66217174(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.598delA
AA Mutation	p.Met200CysfsTer26(p.M200Cfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261233
Start	66245168:66245175(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1224_1231delTCCCTGCC
AA Mutation	p.Pro409SerfsTer27(p.P409Sfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_lost
Transcription ID	ENST00000261233
Start	66248171:66248171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1791A>C
AA Mutation	p.Ter597TyrextTer16(p.597Yext16)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IRAK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261233
Start	66211511:66211511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502G>T
AA Mutation	p.Asp168Tyr(p.D168Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261233
Start	66203794:66203794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.217C>T
AA Mutation	p.Leu73Phe(p.L73F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261233
Start	66228283:66228283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371798024
CDS Mutation	c.800G>A
AA Mutation	p.Arg267Gln(p.R267Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261233
Start	66247721:66247721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1341A>C
AA Mutation	p.Gln447His(p.Q447H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript