Colon Cancer: Gene >> MAP3K10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40192630:40192630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.599C>A
AA Mutation	p.Ala200Asp(p.A200D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40192507:40192507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.476C>T
AA Mutation	p.Ala159Val(p.A159V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40213594:40213594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1915C>T
AA Mutation	p.Pro639Ser(p.P639S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40215235:40215235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2808G>A
AA Mutation	p.Met936Ile(p.M936I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40206131:40206131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1409G>A
AA Mutation	p.Gly470Asp(p.G470D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40215105:40215105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2678G>A
AA Mutation	p.Arg893His(p.R893H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40198410:40198410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202232339
CDS Mutation	c.718G>A
AA Mutation	p.Ala240Thr(p.A240T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40205283:40205283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1175G>A
AA Mutation	p.Arg392Gln(p.R392Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40214976:40214976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149852844
CDS Mutation	c.2549G>A
AA Mutation	p.Arg850His(p.R850H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40204489:40204489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.868G>A
AA Mutation	p.Gly290Arg(p.G290R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253055
Start	40215082:40215082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531778546
CDS Mutation	c.2655G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253055
Start	40198478:40198478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201837585
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253055
Start	40209173:40209173(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1511delC
AA Mutation	p.Pro504LeufsTer10(p.P504Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253055
Start	40213555:40213555(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1880delC
AA Mutation	p.Pro627LeufsTer50(p.P627Lfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000253055
Start	40204633:40204633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1012G>T
AA Mutation	p.Glu338Ter(p.E338*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253055
Start	40215237:40215238(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2814dupG
AA Mutation	p.Gln939AlafsTer29(p.Q939Afs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAP3K10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40198390:40198390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.698C>A
AA Mutation	p.Ala233Asp(p.A233D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40212870:40212870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763193956
CDS Mutation	c.1618C>T
AA Mutation	p.Arg540Cys(p.R540C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253055
Start	40192383:40192383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352C>T
AA Mutation	p.Arg118Cys(p.R118C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript