Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LTBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74585893:74585893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791C>T
AA Mutation	p.Ala264Val(p.A264V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74502886:74502886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4937A>C
AA Mutation	p.Glu1646Ala(p.E1646A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74507211:74507211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3875G>A
AA Mutation	p.Gly1292Asp(p.G1292D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74555650:74555650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874G>A
AA Mutation	p.Val292Met(p.V292M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74509847:74509847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3164G>A
AA Mutation	p.Cys1055Tyr(p.C1055Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74552897:74552897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765793427
CDS Mutation	c.1187G>A
AA Mutation	p.Arg396His(p.R396H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74508900:74508900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3456G>T
AA Mutation	p.Lys1152Asn(p.K1152N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74505123:74505123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543585255
CDS Mutation	c.4229G>A
AA Mutation	p.Arg1410His(p.R1410H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74504004:74504004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4504T>C
AA Mutation	p.Cys1502Arg(p.C1502R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74501005:74501005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5345A>G
AA Mutation	p.Asn1782Ser(p.N1782S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74503309:74503309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768138050
CDS Mutation	c.4798C>T
AA Mutation	p.Arg1600Cys(p.R1600C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74528525:74528525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145507464
CDS Mutation	c.2326G>A
AA Mutation	p.Val776Ile(p.V776I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74551138:74551138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147534770
CDS Mutation	c.1612C>T
AA Mutation	p.Arg538Trp(p.R538W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74501567:74501567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5194C>A
AA Mutation	p.Leu1732Ile(p.L1732I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74529083:74529083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199710871
CDS Mutation	c.2027G>A
AA Mutation	p.Arg676Gln(p.R676Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74502904:74502904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751200478
CDS Mutation	c.4919G>A
AA Mutation	p.Arg1640His(p.R1640H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74508910:74508910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3446G>A
AA Mutation	p.Gly1149Asp(p.G1149D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74509265:74509265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3376C>T
AA Mutation	p.Pro1126Ser(p.P1126S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74586035:74586035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555894027
CDS Mutation	c.649C>T
AA Mutation	p.Arg217Cys(p.R217C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74502925:74502925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4898C>T
AA Mutation	p.Ala1633Val(p.A1633V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74509336:74509336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3305T>C
AA Mutation	p.Val1102Ala(p.V1102A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74586076:74586076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.608G>A
AA Mutation	p.Arg203His(p.R203H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74525219:74525219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2435C>T
AA Mutation	p.Ala812Val(p.A812V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74532459:74532459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1954C>A
AA Mutation	p.Leu652Ile(p.L652I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74611810:74611810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.135G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74551298:74551298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1452C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74509789:74509789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3222C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74501550:74501550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777241198
CDS Mutation	c.5211C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74506810:74506810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113219139
CDS Mutation	c.3921C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74501574:74501574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149587738
CDS Mutation	c.5187C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74532508:74532508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140743368
CDS Mutation	c.1905G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74504848:74504848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4383G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74509750:74509750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139921455
CDS Mutation	c.3261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74521915:74521915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140090189
CDS Mutation	c.2784T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74506184:74506184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772766355
CDS Mutation	c.4041C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74551214:74551214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371191837
CDS Mutation	c.1536G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261978
Start	74500904:74500904(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5446delC
AA Mutation	p.His1816ThrfsTer32(p.H1816Tfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261978
Start	74549896:74549896(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776807257
CDS Mutation	c.1756delG
AA Mutation	p.Val586Ter(p.V586*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261978
Start	74509273:74509273(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3368delG
AA Mutation	p.Gly1123AlafsTer55(p.G1123Afs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261978
Start	74508690:74508691(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3565dupC
AA Mutation	p.His1189ProfsTer57(p.H1189Pfs*57)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LTBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74511356:74511356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2917G>A
AA Mutation	p.Glu973Lys(p.E973K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74508707:74508707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3549G>T
AA Mutation	p.Glu1183Asp(p.E1183D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261978
Start	74529072:74529072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2038C>T
AA Mutation	p.Pro680Ser(p.P680S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261978
Start	74532541:74532541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149576879
CDS Mutation	c.1872C>T
Mutation Classification	Silent
Feature Type	Transcript