Colon Cancer: Gene >> MAP3K11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65598595:65598595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569473618
CDS Mutation	c.2240G>A
AA Mutation	p.Arg747His(p.R747H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65598607:65598607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2228C>T
AA Mutation	p.Pro743Leu(p.P743L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65599490:65599490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763348971
CDS Mutation	c.2110G>A
AA Mutation	p.Asp704Asn(p.D704N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65608023:65608023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968G>A
AA Mutation	p.Arg323His(p.R323H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65599757:65599757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1843C>T
AA Mutation	p.Arg615Trp(p.R615W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65613101:65613101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656C>T
AA Mutation	p.Ala219Val(p.A219V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65598484:65598484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2351C>T
AA Mutation	p.Ala784Val(p.A784V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65598518:65598518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763537644
CDS Mutation	c.2317C>T
AA Mutation	p.Arg773Cys(p.R773C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65599483:65599483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201727045
CDS Mutation	c.2117C>T
AA Mutation	p.Pro706Leu(p.P706L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309100
Start	65607806:65607806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1080G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309100
Start	65599482:65599482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751664849
CDS Mutation	c.2118G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309100
Start	65599491:65599491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370501486
CDS Mutation	c.2109C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309100
Start	65599563:65599563(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2037delC
AA Mutation	p.Thr680ArgfsTer267(p.T680Rfs*267)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309100
Start	65606037:65606037(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1648delC
AA Mutation	p.Arg550AspfsTer51(p.R550Dfs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000309100
Start	65606004:65606004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1681C>T
AA Mutation	p.Arg561Ter(p.R561*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309100
Start	65598363:65598364(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2471dupG
AA Mutation	p.Gln826ProfsTer36(p.Q826Pfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAP3K11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65613312:65613312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445G>A
AA Mutation	p.Asp149Asn(p.D149N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65608023:65608023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.968G>A
AA Mutation	p.Arg323His(p.R323H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309100
Start	65608343:65608343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.845C>T
AA Mutation	p.Ala282Val(p.A282V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript