Colon Cancer: Gene >> MAP1S

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17726398:17726398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1014C>A
AA Mutation	p.Phe338Leu(p.F338L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17727747:17727747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2363G>A
AA Mutation	p.Ser788Asn(p.S788N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17727729:17727729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2345C>T
AA Mutation	p.Thr782Met(p.T782M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17727057:17727057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757253194
CDS Mutation	c.1673C>T
AA Mutation	p.Ala558Val(p.A558V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17733417:17733417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373990918
CDS Mutation	c.3013C>T
AA Mutation	p.Arg1005Cys(p.R1005C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17726907:17726907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1523G>A
AA Mutation	p.Arg508Gln(p.R508Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17727045:17727045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1661C>T
AA Mutation	p.Thr554Met(p.T554M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17733387:17733387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2983G>A
AA Mutation	p.Ala995Thr(p.A995T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17726142:17726142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758C>T
AA Mutation	p.Ala253Val(p.A253V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17734346:17734346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3098C>T
AA Mutation	p.Ala1033Val(p.A1033V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17726753:17726753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1369C>T
AA Mutation	p.Pro457Ser(p.P457S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17733397:17733397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2993C>T
AA Mutation	p.Ala998Val(p.A998V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17727294:17727294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1910G>A
AA Mutation	p.Arg637His(p.R637H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324096
Start	17720964:17720964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750930809
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324096
Start	17725127:17725127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324096
Start	17727944:17727944(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2560delC
AA Mutation	p.Arg854GlyfsTer156(p.R854Gfs*156)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324096
Start	17725972:17725972(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.593delC
AA Mutation	p.Pro198ArgfsTer93(p.P198Rfs*93)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324096
Start	17727160:17727160(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1782delC
AA Mutation	p.Ser595ValfsTer62(p.S595Vfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000324096
Start	17725948:17725953(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs746787027
CDS Mutation	c.569_574delGGCTCC
AA Mutation	p.Arg190_Leu191del(p.R190_L191del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAP1S

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17733313:17733313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757937252
CDS Mutation	c.2909G>A
AA Mutation	p.Arg970His(p.R970H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324096
Start	17721021:17721021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204C>A
AA Mutation	p.Phe68Leu(p.F68L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript