Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LILRB1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54636804:54636804(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1885A>G
AA Mutation p.Thr629Ala(p.T629A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54631610:54631610(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.181T>C
AA Mutation p.Tyr61His(p.Y61H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54631712:54631712(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147024305
CDS Mutation c.283C>T
AA Mutation p.Arg95Trp(p.R95W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54632535:54632535(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.733C>A
AA Mutation p.Gln245Lys(p.Q245K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54636858:54636858(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199564534
CDS Mutation c.1939G>A
AA Mutation p.Ala647Thr(p.A647T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54635153:54635153(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1536G>T
AA Mutation p.Glu512Asp(p.E512D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54631971:54631971(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.395G>T
AA Mutation p.Ser132Ile(p.S132I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54631671:54631671(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.242G>A
AA Mutation p.Gly81Asp(p.G81D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54632148:54632148(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs543166769
CDS Mutation c.572G>A
AA Mutation p.Arg191His(p.R191H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000324602
Start 54633080:54633080(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201120319
CDS Mutation c.1023C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000324602
Start 54631616:54631616(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.187G>T
AA Mutation p.Glu63Ter(p.E63*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000324602
Start 54633158:54633158(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1101G>A
AA Mutation p.Trp367Ter(p.W367*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000324602
Start 54631723:54631724(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.294_295insA
AA Mutation p.Tyr99IlefsTer4(p.Y99Ifs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> LILRB1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54633137:54633137(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1080G>T
AA Mutation p.Glu360Asp(p.E360D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54632185:54632185(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.609C>A
AA Mutation p.Asn203Lys(p.N203K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54633245:54633245(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1188G>T
AA Mutation p.Arg396Ser(p.R396S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000324602
Start 54633686:54633686(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1310C>A
AA Mutation p.Ser437Tyr(p.S437Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54636796:54636796(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753349590
CDS Mutation c.1877G>A
AA Mutation p.Arg626Gln(p.R626Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000324602
Start 54633187:54633187(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1130A>C
AA Mutation p.Lys377Thr(p.K377T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000324602
Start 54636767:54636767(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771848801
CDS Mutation c.1848C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000324602
Start 54633137:54633137(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1080G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000324602
Start 54634669:54634669(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200419876
CDS Mutation c.1392C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000324602
Start 54635287:54635287(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1591G>T
AA Mutation p.Glu531Ter(p.E531*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript