Colon Cancer: Gene >> SELP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169593620:169593620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749608555
CDS Mutation	c.2392C>T
AA Mutation	p.Arg798Cys(p.R798C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169607078:169607078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390C>T
AA Mutation	p.Pro464Ser(p.P464S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169612349:169612349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829C>A
AA Mutation	p.His277Asn(p.H277N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169619186:169619186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.37T>A
AA Mutation	p.Phe13Ile(p.F13I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169603079:169603079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1652G>T
AA Mutation	p.Arg551Ile(p.R551I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169613657:169613657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.518A>G
AA Mutation	p.Glu173Gly(p.E173G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169611627:169611627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1012G>A
AA Mutation	p.Val338Ile(p.V338I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169609587:169609587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1250C>T
AA Mutation	p.Ala417Val(p.A417V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169594848:169594848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2131A>G
AA Mutation	p.Lys711Glu(p.K711E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169596050:169596050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1976C>T
AA Mutation	p.Pro659Leu(p.P659L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169609552:169609552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285C>T
AA Mutation	p.Arg429Trp(p.R429W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169617322:169617322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753097216
CDS Mutation	c.187C>T
AA Mutation	p.Arg63Cys(p.R63C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169593670:169593670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2342C>A
AA Mutation	p.Ser781Tyr(p.S781Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169590171:169590171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755777385
CDS Mutation	c.2470G>A
AA Mutation	p.Ala824Thr(p.A824T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263686
Start	169609673:169609673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145714766
CDS Mutation	c.1164G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263686
Start	169617101:169617101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263686
Start	169594861:169594861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2118A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263686
Start	169607079:169607079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1389C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263686
Start	169611496:169611496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780415483
CDS Mutation	c.1143T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263686
Start	169619172:169619172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.51C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263686
Start	169594799:169594800(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2179_2180delGG
AA Mutation	p.Gly727IlefsTer14(p.G727Ifs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000263686
Start	169617356:169617356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.153C>A
AA Mutation	p.Tyr51Ter(p.Y51*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263686
Start	169594800:169594801(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2178_2179insTTTCCAC
AA Mutation	p.Gly727PhefsTer17(p.G727Ffs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SELP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169597074:169597074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1808A>G
AA Mutation	p.Asp603Gly(p.D603G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169603088:169603088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1643G>A
AA Mutation	p.Gly548Glu(p.G548E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169612944:169612944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.760C>A
AA Mutation	p.Pro254Thr(p.P254T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263686
Start	169619179:169619179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44G>C
AA Mutation	p.Arg15Thr(p.R15T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263686
Start	169611523:169611523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263686
Start	169596064:169596064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1962C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263686
Start	169611574:169611574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1065G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000263686
Start	169613626:169613626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549C>A
AA Mutation	p.Cys183Ter(p.C183*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript