Colon Cancer: Gene >> INO80

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361937
Start	41056702:41056702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1990C>A
AA Mutation	p.Arg664Ser(p.R664S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361937
Start	40982919:40982919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4396G>A
AA Mutation	p.Gly1466Arg(p.G1466R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361937
Start	41045023:41045023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572481309
CDS Mutation	c.2788C>T
AA Mutation	p.Arg930Cys(p.R930C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361937
Start	41085515:41085515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548696805
CDS Mutation	c.727C>T
AA Mutation	p.Arg243Cys(p.R243C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361937
Start	41054014:41054014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2189A>G
AA Mutation	p.Asn730Ser(p.N730S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361937
Start	41005671:41005671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3419G>T
AA Mutation	p.Arg1140Met(p.R1140M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361937
Start	41092106:41092106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458G>T
AA Mutation	p.Ser153Ile(p.S153I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361937
Start	41096265:41096265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755496508
CDS Mutation	c.46C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361937
Start	40997592:40997592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3507C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361937
Start	41059923:41059923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1786C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361937
Start	40984322:40984322(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3952delA
AA Mutation	p.Arg1318GlyfsTer6(p.R1318Gfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000361937
Start	41069631:41069631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1721C>A
AA Mutation	p.Ser574Ter(p.S574*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000361937
Start	41069651:41069651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1701G>A
AA Mutation	p.Trp567Ter(p.W567*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361937
Start	41048233:41048234(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2619_2620insAT
AA Mutation	p.Arg874IlefsTer42(p.R874Ifs*42)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000361937
Start	40982872:40982874(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4441_4443delAAC
AA Mutation	p.Asn1481del(p.N1481del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> INO80

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361937
Start	41050005:41050005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2372C>A
AA Mutation	p.Ser791Tyr(p.S791Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361937
Start	41055271:41055271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2164G>A
AA Mutation	p.Glu722Lys(p.E722K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361937
Start	41092079:41092079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755595019
CDS Mutation	c.485G>A
AA Mutation	p.Arg162Gln(p.R162Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript