Colon Cancer: Gene >> CD93

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23085462:23085462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.731C>T
AA Mutation	p.Ala244Val(p.A244V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23084320:23084320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1873G>A
AA Mutation	p.Ala625Thr(p.A625T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23084710:23084710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1483C>T
AA Mutation	p.Pro495Ser(p.P495S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23084892:23084892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41520247
CDS Mutation	c.1301C>T
AA Mutation	p.Pro434Leu(p.P434L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23085355:23085355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763943573
CDS Mutation	c.838G>A
AA Mutation	p.Asp280Asn(p.D280N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23085753:23085753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440A>T
AA Mutation	p.Asp147Val(p.D147V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23085409:23085409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.784T>C
AA Mutation	p.Tyr262His(p.Y262H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23085184:23085184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009G>A
AA Mutation	p.Asp337Asn(p.D337N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23084706:23084706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570911199
CDS Mutation	c.1487G>A
AA Mutation	p.Arg496His(p.R496H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23084401:23084401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1792G>A
AA Mutation	p.Ala598Thr(p.A598T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23085466:23085466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.727A>C
AA Mutation	p.Lys243Gln(p.K243Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23084373:23084373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769815543
CDS Mutation	c.1820G>A
AA Mutation	p.Arg607His(p.R607H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23086090:23086090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103G>A
AA Mutation	p.Ala35Thr(p.A35T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23085435:23085435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761695801
CDS Mutation	c.758C>T
AA Mutation	p.Ser253Leu(p.S253L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23085319:23085319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874C>G
AA Mutation	p.Arg292Gly(p.R292G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23085241:23085241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140540216
CDS Mutation	c.952G>A
AA Mutation	p.Val318Ile(p.V318I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246006
Start	23084960:23084960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1233T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246006
Start	23085005:23085005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747076730
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246006
Start	23085668:23085668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.525T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246006
Start	23084633:23084633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745870867
CDS Mutation	c.1560G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246006
Start	23085832:23085832(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs762805003
CDS Mutation	c.361delG
AA Mutation	p.Glu121ArgfsTer79(p.E121Rfs*79)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246006
Start	23084750:23084750(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1443delC
AA Mutation	p.Asp482MetfsTer106(p.D482Mfs*106)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246006
Start	23085355:23085355(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.838delG
AA Mutation	p.Asp280MetfsTer19(p.D280Mfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246006
Start	23086020:23086020(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.173delG
AA Mutation	p.Gly58AlafsTer6(p.G58Afs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000246006
Start	23085005:23085005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1188C>A
AA Mutation	p.Cys396Ter(p.C396*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000246006
Start	23085249:23085250(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs747115137
CDS Mutation	c.943dupG
AA Mutation	p.Ala315GlyfsTer34(p.A315Gfs*34)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CD93

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23085259:23085259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762071141
CDS Mutation	c.934C>T
AA Mutation	p.Arg312Cys(p.R312C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23083969:23083969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940C>A
AA Mutation	p.Thr647Lys(p.T647K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000246006
Start	23085534:23085534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138932459
CDS Mutation	c.659C>T
AA Mutation	p.Ala220Val(p.A220V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000246006
Start	23086049:23086049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript