Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> VAV3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107603126:107603126(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139894223
CDS Mutation c.2053G>A
AA Mutation p.Glu685Lys(p.E685K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107617591:107617591(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1956T>G
AA Mutation p.Ser652Arg(p.S652R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107875014:107875014(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.208C>A
AA Mutation p.Leu70Ile(p.L70I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107749024:107749024(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1446T>G
AA Mutation p.Phe482Leu(p.F482L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107964725:107964725(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753063166
CDS Mutation c.145A>C
AA Mutation p.Asn49His(p.N49H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107770694:107770694(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.590T>C
AA Mutation p.Leu197Pro(p.L197P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107749023:107749023(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1447T>A
AA Mutation p.Tyr483Asn(p.Y483N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107704623:107704623(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1632T>G
AA Mutation p.Cys544Trp(p.C544W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107964679:107964679(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.191C>T
AA Mutation p.Pro64Leu(p.P64L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107964862:107964862(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372314733
CDS Mutation c.8C>T
AA Mutation p.Pro3Leu(p.P3L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107964715:107964715(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.155C>T
AA Mutation p.Ala52Val(p.A52V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107779452:107779452(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.362C>T
AA Mutation p.Ala121Val(p.A121V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107688401:107688401(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1711G>A
AA Mutation p.Gly571Arg(p.G571R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000370056
Start 107874901:107874901(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.321G>T
AA Mutation p.Lys107Asn(p.K107N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107617577:107617577(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1970C>A
AA Mutation p.Pro657His(p.P657H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000370056
Start 107964841:107964841(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.29G>A
AA Mutation p.Trp10Ter(p.W10*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence stop_gained
Transcription ID ENST00000370056
Start 107617573:107617573(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1974C>A
AA Mutation p.Cys658Ter(p.C658*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence stop_gained
Transcription ID ENST00000370056
Start 107779465:107779465(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.349C>T
AA Mutation p.Arg117Ter(p.R117*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> VAV3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107874993:107874993(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.229A>G
AA Mutation p.Thr77Ala(p.T77A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107964833:107964833(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.37C>A
AA Mutation p.His13Asn(p.H13N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370056
Start 107751153:107751153(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377138310
CDS Mutation c.1223G>A
AA Mutation p.Arg408Gln(p.R408Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000370056
Start 107705059:107705059(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750852069
CDS Mutation c.1505C>A
AA Mutation p.Ser502Tyr(p.S502Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000370056
Start 107755481:107755481(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1119A>G
Mutation Classification Silent
Feature Type Transcript