Colon Cancer: Gene >> MCM10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13195243:13195243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1951C>A
AA Mutation	p.Leu651Met(p.L651M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13175674:13175674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752987555
CDS Mutation	c.760C>T
AA Mutation	p.Arg254Trp(p.R254W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13175573:13175573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756598324
CDS Mutation	c.659G>A
AA Mutation	p.Arg220Gln(p.R220Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13191388:13191388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368268628
CDS Mutation	c.1508G>A
AA Mutation	p.Arg503Gln(p.R503Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13209099:13209099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544718421
CDS Mutation	c.2510G>A
AA Mutation	p.Gly837Asp(p.G837D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13191319:13191319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1439A>G
AA Mutation	p.Lys480Arg(p.K480R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13171065:13171065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533521913
CDS Mutation	c.151G>A
AA Mutation	p.Asp51Asn(p.D51N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13197691:13197691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2046G>T
AA Mutation	p.Lys682Asn(p.K682N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13192312:13192312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758103796
CDS Mutation	c.1577C>T
AA Mutation	p.Pro526Leu(p.P526L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13171122:13171122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779760770
CDS Mutation	c.208G>A
AA Mutation	p.Glu70Lys(p.E70K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000484800
Start	13172443:13172443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000484800
Start	13195083:13195083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1791A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000484800
Start	13172698:13172698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150854146
CDS Mutation	c.528G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000484800
Start	13175613:13175613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.699G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000484800
Start	13195167:13195167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144824319
CDS Mutation	c.1875G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000484800
Start	13197741:13197741(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2102delA
AA Mutation	p.Asn701ThrfsTer35(p.N701Tfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000484800
Start	13175629:13175629(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.718delG
AA Mutation	p.Glu240LysfsTer26(p.E240Kfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000484800
Start	13198715:13198715(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2155delA
AA Mutation	p.Arg719GlyfsTer17(p.R719Gfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000484800
Start	13195180:13195180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148160347
CDS Mutation	c.1888C>T
AA Mutation	p.Arg630Ter(p.R630*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000484800
Start	13171089:13171090(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.175_176insTGGCCTAGAGGCCAAATGTTTTTTGTTTGGCTTACAGAATTAGATTA
AA Mutation	p.Ala59ValfsTer3(p.A59Vfs*3)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000484800
Start	13209112:13209112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2523G>A
AA Mutation	p.Trp841Ter(p.W841*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000484800
Start	13172474:13172475(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.448_449insGCGGG
AA Mutation	p.Ser150CysfsTer5(p.S150Cfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000484800
Start	13171173:13171175(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs531543734
CDS Mutation	c.266_268delAAG
AA Mutation	p.Glu89del(p.E89del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MCM10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13191336:13191336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1456A>G
AA Mutation	p.Thr486Ala(p.T486A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13209284:13209284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2602G>A
AA Mutation	p.Ala868Thr(p.A868T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000484800
Start	13192299:13192299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1564C>A
AA Mutation	p.Leu522Met(p.L522M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript