Colon Cancer: Gene >> OGDH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44701574:44701574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2591G>A
AA Mutation	p.Arg864His(p.R864H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44697375:44697375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2057G>A
AA Mutation	p.Arg686His(p.R686H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44694530:44694530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1622C>T
AA Mutation	p.Ala541Val(p.A541V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44674458:44674458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.836G>T
AA Mutation	p.Gly279Val(p.G279V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44707697:44707697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2912C>T
AA Mutation	p.Pro971Leu(p.P971L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44700262:44700262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2552G>A
AA Mutation	p.Arg851Gln(p.R851Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44676072:44676072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1129C>T
AA Mutation	p.Leu377Phe(p.L377F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44701573:44701573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2590C>T
AA Mutation	p.Arg864Cys(p.R864C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44707706:44707706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2921G>A
AA Mutation	p.Arg974Gln(p.R974Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44707916:44707916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2989G>A
AA Mutation	p.Gly997Ser(p.G997S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44707333:44707333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2741G>A
AA Mutation	p.Arg914Gln(p.R914Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44624485:44624485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142C>T
AA Mutation	p.Pro48Ser(p.P48S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44645344:44645344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758752503
CDS Mutation	c.240T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44701557:44701557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2574C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44624529:44624529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.186C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44696445:44696445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756317172
CDS Mutation	c.1788C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44693962:44693962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534693220
CDS Mutation	c.1473C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44697487:44697487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781065314
CDS Mutation	c.2169C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44681776:44681776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759170384
CDS Mutation	c.1263C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44697737:44697737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2313G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222673
Start	44647686:44647686(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.448delC
AA Mutation	p.Leu150TrpfsTer131(p.L150Wfs*131)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000222673
Start	44693944:44693944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1455C>A
AA Mutation	p.Tyr485Ter(p.Y485*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222673
Start	44707628:44707629(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2847dupC
AA Mutation	p.Asn950GlnfsTer3(p.N950Qfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> OGDH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44666825:44666825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.607C>A
AA Mutation	p.Leu203Met(p.L203M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222673
Start	44707641:44707641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2856G>T
AA Mutation	p.Glu952Asp(p.E952D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44697490:44697490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2172C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222673
Start	44676080:44676080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145890791
CDS Mutation	c.1137C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222673
Start	44675217:44675217(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.975delG
AA Mutation	p.Glu325AspfsTer23(p.E325Dfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript