Colon Cancer: Gene >> CD163

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7499164:7499164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.482T>C
AA Mutation	p.Leu161Pro(p.L161P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7487392:7487392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2017C>T
AA Mutation	p.Pro673Ser(p.P673S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7487551:7487551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1858C>A
AA Mutation	p.Leu620Ile(p.L620I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7486580:7486580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2377T>A
AA Mutation	p.Ser793Thr(p.S793T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7502483:7502483(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128C>A
AA Mutation	p.Ser43Tyr(p.S43Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7479992:7479992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3348T>A
AA Mutation	p.Asn1116Lys(p.N1116K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7485376:7485376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2499G>T
AA Mutation	p.Glu833Asp(p.E833D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7481240:7481240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3264G>T
AA Mutation	p.Glu1088Asp(p.E1088D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7488015:7488015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1493C>A
AA Mutation	p.Thr498Lys(p.T498K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7496975:7496975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757801947
CDS Mutation	c.937G>A
AA Mutation	p.Val313Ile(p.V313I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7487610:7487610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374281824
CDS Mutation	c.1799C>T
AA Mutation	p.Thr600Met(p.T600M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7499017:7499017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.629G>C
AA Mutation	p.Gly210Ala(p.G210A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7499018:7499018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.628G>T
AA Mutation	p.Gly210Cys(p.G210C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7479958:7479958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3382C>A
AA Mutation	p.Leu1128Ile(p.L1128I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7495359:7495359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780185045
CDS Mutation	c.1142G>A
AA Mutation	p.Arg381His(p.R381H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7482666:7482666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748750295
CDS Mutation	c.3224G>A
AA Mutation	p.Arg1075Gln(p.R1075Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7482714:7482714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3176T>C
AA Mutation	p.Val1059Ala(p.V1059A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7483652:7483652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2803C>T
AA Mutation	p.Pro935Ser(p.P935S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7487403:7487403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2006C>T
AA Mutation	p.Ala669Val(p.A669V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7495285:7495285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1216G>A
AA Mutation	p.Glu406Lys(p.E406K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7485362:7485362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2513G>A
AA Mutation	p.Arg838His(p.R838H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7481202:7481202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3302C>A
AA Mutation	p.Ser1101Tyr(p.S1101Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7483447:7483447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3008C>A
AA Mutation	p.Ser1003Tyr(p.S1003Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7483593:7483593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2862T>G
AA Mutation	p.Cys954Trp(p.C954W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7483385:7483385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145413017
CDS Mutation	c.3070G>A
AA Mutation	p.Ala1024Thr(p.A1024T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359156
Start	7497045:7497045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359156
Start	7486716:7486716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2241C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359156
Start	7496976:7496976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749090106
CDS Mutation	c.936C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359156
Start	7501413:7501413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772059973
CDS Mutation	c.183C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359156
Start	7486949:7486949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536972277
CDS Mutation	c.2088G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359156
Start	7486904:7486904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2133G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359156
Start	7496952:7496952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138251842
CDS Mutation	c.960C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359156
Start	7485348:7485348(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2527delT
AA Mutation	p.Tyr843ThrfsTer38(p.Y843Tfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359156
Start	7479915:7479915(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3425delA
AA Mutation	p.Lys1142ArgfsTer5(p.K1142Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000359156
Start	7496863:7496863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1049G>A
AA Mutation	p.Trp350Ter(p.W350*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CD163

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7479979:7479979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3361G>T
AA Mutation	p.Ala1121Ser(p.A1121S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7495353:7495353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1148C>T
AA Mutation	p.Ala383Val(p.A383V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7485191:7485191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2684G>T
AA Mutation	p.Cys895Phe(p.C895F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7487535:7487535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1874A>G
AA Mutation	p.Lys625Arg(p.K625R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359156
Start	7499022:7499022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624C>A
AA Mutation	p.Phe208Leu(p.F208L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359156
Start	7483398:7483398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3057G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359156
Start	7486554:7486554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2403C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359156
Start	7485331:7485331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2544C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000359156
Start	7487665:7487665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744G>T
AA Mutation	p.Glu582Ter(p.E582*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript