Colon Cancer: Gene >> STAG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136359232:136359232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2852G>T
AA Mutation	p.Gly951Val(p.G951V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136521329:136521329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535245987
CDS Mutation	c.560G>A
AA Mutation	p.Arg187Gln(p.R187Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136568813:136568813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757393709
CDS Mutation	c.346G>A
AA Mutation	p.Ala116Thr(p.A116T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136398790:136398790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2236C>T
AA Mutation	p.Leu746Phe(p.L746F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136472482:136472482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1136T>C
AA Mutation	p.Val379Ala(p.V379A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136422451:136422451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1996G>T
AA Mutation	p.Val666Leu(p.V666L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136359215:136359215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2869C>T
AA Mutation	p.Arg957Cys(p.R957C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136542123:136542123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.467A>G
AA Mutation	p.Asp156Gly(p.D156G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136604356:136604356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250C>T
AA Mutation	p.Pro84Ser(p.P84S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136338422:136338422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3701C>T
AA Mutation	p.Ala1234Val(p.A1234V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136502636:136502636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820C>T
AA Mutation	p.Arg274Cys(p.R274C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136341489:136341489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3509G>T
AA Mutation	p.Arg1170Ile(p.R1170I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136422565:136422565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774492433
CDS Mutation	c.1882G>A
AA Mutation	p.Val628Ile(p.V628I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136521365:136521365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524G>T
AA Mutation	p.Arg175Leu(p.R175L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136500276:136500276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.849A>C
AA Mutation	p.Glu283Asp(p.E283D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136542171:136542171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774614550
CDS Mutation	c.419G>A
AA Mutation	p.Arg140Gln(p.R140Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136341474:136341474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3524A>G
AA Mutation	p.Tyr1175Cys(p.Y1175C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136443340:136443340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1493A>G
AA Mutation	p.Asp498Gly(p.D498G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136521366:136521366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756848648
CDS Mutation	c.523C>T
AA Mutation	p.Arg175Cys(p.R175C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136521381:136521381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508C>G
AA Mutation	p.Gln170Glu(p.Q170E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136477329:136477329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.986A>G
AA Mutation	p.Asp329Gly(p.D329G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383202
Start	136473602:136473602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1062G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383202
Start	136349357:136349357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3072A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383202
Start	136357743:136357743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3042T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383202
Start	136500273:136500273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779336188
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383202
Start	136349168:136349168(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3261delA
AA Mutation	p.Lys1087AsnfsTer3(p.K1087Nfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000383202
Start	136500249:136500249(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.876delT
AA Mutation	p.Phe292LeufsTer28(p.F292Lfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000383202
Start	136542172:136542172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418C>T
AA Mutation	p.Arg140Ter(p.R140*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000383202
Start	136357739:136357739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3046C>T
AA Mutation	p.Arg1016Ter(p.R1016*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000383202
Start	136521330:136521330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Ter(p.R187*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000383202
Start	136422445:136422445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2002C>T
AA Mutation	p.Arg668Ter(p.R668*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000383202
Start	136422475:136422475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1972C>T
AA Mutation	p.Arg658Ter(p.R658*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> STAG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136502678:136502678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778G>A
AA Mutation	p.Gly260Arg(p.G260R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136359212:136359212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2872C>T
AA Mutation	p.Arg958Cys(p.R958C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000383202
Start	136338435:136338435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3688C>T
AA Mutation	p.Arg1230Trp(p.R1230W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000383202
Start	136502711:136502711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000383202
Start	136521330:136521330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559C>T
AA Mutation	p.Arg187Ter(p.R187*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript