Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FYN

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111702966:111702966(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.616C>T
AA Mutation p.Arg206Cys(p.R206C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111674532:111674532(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1372G>A
AA Mutation p.Glu458Lys(p.E458K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000354650
Start 111700104:111700104(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.862G>A
AA Mutation p.Gly288Ser(p.G288S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000354650
Start 111694628:111694628(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1119G>T
AA Mutation p.Gln373His(p.Q373H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111703013:111703013(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756342493
CDS Mutation c.569G>A
AA Mutation p.Arg190His(p.R190H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111719925:111719925(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144813746
CDS Mutation c.127G>A
AA Mutation p.Gly43Ser(p.G43S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111719823:111719823(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746134687
CDS Mutation c.229C>T
AA Mutation p.Arg77Cys(p.R77C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111700197:111700197(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.769T>C
AA Mutation p.Ser257Pro(p.S257P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000354650
Start 111700213:111700213(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.753A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000354650
Start 111719992:111719992(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.60C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000354650
Start 111661865:111661865(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1488T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000354650
Start 111704065:111704065(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.481C>T
AA Mutation p.Arg161Ter(p.R161*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000354650
Start 111720024:111720024(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.28G>T
AA Mutation p.Glu10Ter(p.E10*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000354650
Start 111661838:111661839(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1514dupA
AA Mutation p.Asp506GlyfsTer3(p.D506Gfs*3)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 15
Mutation Consequence splice_donor_variant
Transcription ID ENST00000354650
Start 111700102:111700102(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.862+2T>G
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> FYN

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111702966:111702966(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.616C>T
AA Mutation p.Arg206Cys(p.R206C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000354650
Start 111719896:111719896(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.156C>A
AA Mutation p.Asn52Lys(p.N52K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000354650
Start 111719965:111719965(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.87C>A
Mutation Classification Silent
Feature Type Transcript