Colon Cancer: Gene >> MINK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355280
Start	4896703:4896703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3805T>C
AA Mutation	p.Trp1269Arg(p.W1269R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355280
Start	4896323:4896323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3596A>G
AA Mutation	p.Asp1199Gly(p.D1199G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355280
Start	4892497:4892497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751020945
CDS Mutation	c.2183C>T
AA Mutation	p.Pro728Leu(p.P728L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355280
Start	4886605:4886605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928C>T
AA Mutation	p.Arg310Trp(p.R310W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355280
Start	4896520:4896520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3707A>G
AA Mutation	p.Tyr1236Cys(p.Y1236C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355280
Start	4887699:4887699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1139A>C
AA Mutation	p.Gln380Pro(p.Q380P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355280
Start	4894092:4894092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528570871
CDS Mutation	c.2669G>A
AA Mutation	p.Arg890His(p.R890H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355280
Start	4895098:4895098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2941C>T
AA Mutation	p.Arg981Trp(p.R981W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000355280
Start	4886174:4886174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.749C>T
AA Mutation	p.Pro250Leu(p.P250L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000355280
Start	4889699:4889699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283G>A
AA Mutation	p.Arg428Gln(p.R428Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000355280
Start	4894002:4894002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2579C>T
AA Mutation	p.Thr860Ile(p.T860I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000355280
Start	4894556:4894556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2840G>T
AA Mutation	p.Gly947Val(p.G947V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355280
Start	4891079:4891079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1695T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355280
Start	4890642:4890642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1473G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355280
Start	4889751:4889751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761158332
CDS Mutation	c.1335G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355280
Start	4892704:4892704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758507498
CDS Mutation	c.2247C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355280
Start	4894233:4894233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2730T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355280
Start	4897207:4897207(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3924delT
AA Mutation	p.Phe1308LeufsTer15(p.F1308Lfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355280
Start	4896565:4896565(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3757delG
AA Mutation	p.Glu1253ArgfsTer14(p.E1253Rfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355280
Start	4892425:4892425(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2113delA
AA Mutation	p.Ile705SerfsTer101(p.I705Sfs*101)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000355280
Start	4895436:4895436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3172C>T
AA Mutation	p.Arg1058Ter(p.R1058*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000355280
Start	4895797:4895798(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3334dupG
AA Mutation	p.Asp1112GlyfsTer17(p.D1112Gfs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MINK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355280
Start	4896035:4896035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3397G>A
AA Mutation	p.Ala1133Thr(p.A1133T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355280
Start	4887631:4887631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1071G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000355280
Start	4886143:4886143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.718C>T
AA Mutation	p.Arg240Ter(p.R240*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript