Colon Cancer: Gene >> MAP9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155373188:155373188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.429A>C
AA Mutation	p.Lys143Asn(p.K143N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155368590:155368590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704C>T
AA Mutation	p.Pro235Leu(p.P235L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155373236:155373236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.381A>C
AA Mutation	p.Lys127Asn(p.K127N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155373250:155373250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.367G>C
AA Mutation	p.Asp123His(p.D123H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155355877:155355877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129A>G
AA Mutation	p.Thr377Ala(p.T377A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155347826:155347826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749611120
CDS Mutation	c.1901C>T
AA Mutation	p.Pro634Leu(p.P634L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155353307:155353307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1414T>G
AA Mutation	p.Ser472Ala(p.S472A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155355805:155355805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772352395
CDS Mutation	c.1201G>A
AA Mutation	p.Gly401Arg(p.G401R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311277
Start	155360357:155360357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.861G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311277
Start	155355830:155355830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762649412
CDS Mutation	c.1176G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311277
Start	155352717:155352717(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1700delA
AA Mutation	p.Lys567ArgfsTer13(p.K567Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311277
Start	155373400:155373400(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs747860737
CDS Mutation	c.217delA
AA Mutation	p.Met73Ter(p.M73*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311277
Start	155352638:155352638(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1779delA
AA Mutation	p.Asp594IlefsTer82(p.D594Ifs*82)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000311277
Start	155347875:155347875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137869187
CDS Mutation	c.1852C>T
AA Mutation	p.Arg618Ter(p.R618*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311277
Start	155352637:155352638(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs763048175
CDS Mutation	c.1779dupA
AA Mutation	p.Asp594ArgfsTer2(p.D594Rfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAP9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155357516:155357516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054A>G
AA Mutation	p.Thr352Ala(p.T352A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155373231:155373231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.386T>G
AA Mutation	p.Phe129Cys(p.F129C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155347885:155347885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1842A>C
AA Mutation	p.Glu614Asp(p.E614D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155355868:155355868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1138T>C
AA Mutation	p.Phe380Leu(p.F380L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155355775:155355775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1231T>C
AA Mutation	p.Ser411Pro(p.S411P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311277
Start	155373360:155373360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257C>A
AA Mutation	p.Pro86His(p.P86H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript