Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FGA

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154584339:154584339(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2386G>A
AA Mutation p.Glu796Lys(p.E796K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154584750:154584750(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748964321
CDS Mutation c.1975T>G
AA Mutation p.Phe659Val(p.F659V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154589514:154589514(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs121909606
CDS Mutation c.103C>T
AA Mutation p.Arg35Cys(p.R35C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154584636:154584636(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771023837
CDS Mutation c.2089G>A
AA Mutation p.Gly697Ser(p.G697S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154589556:154589556(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.61G>T
AA Mutation p.Asp21Tyr(p.D21Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154585949:154585949(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1480G>A
AA Mutation p.Ala494Thr(p.A494T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000302053
Start 154587512:154587512(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.510G>T
AA Mutation p.Glu170Asp(p.E170D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154586057:154586057(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1372C>T
AA Mutation p.Arg458Cys(p.R458C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154586701:154586701(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.728A>G
AA Mutation p.Lys243Arg(p.K243R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154588943:154588943(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.214G>T
AA Mutation p.Gly72Trp(p.G72W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154586798:154586798(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.631G>T
AA Mutation p.Asp211Tyr(p.D211Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154584527:154584527(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2198G>A
AA Mutation p.Gly733Glu(p.G733E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154585868:154585868(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755603154
CDS Mutation c.1561G>A
AA Mutation p.Asp521Asn(p.D521N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000302053
Start 154584634:154584634(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2091C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000302053
Start 154586223:154586223(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768140528
CDS Mutation c.1206C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000302053
Start 154586127:154586127(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1302C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000302053
Start 154586220:154586220(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775218633
CDS Mutation c.1209G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000302053
Start 154586328:154586328(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747858344
CDS Mutation c.1101C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000302053
Start 154589518:154589518(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758959148
CDS Mutation c.99C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence stop_gained
Transcription ID ENST00000302053
Start 154586466:154586466(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.963G>A
AA Mutation p.Trp321Ter(p.W321*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence stop_gained
Transcription ID ENST00000302053
Start 154586897:154586897(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140911890
CDS Mutation c.532C>T
AA Mutation p.Arg178Ter(p.R178*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence frameshift_variant
Transcription ID ENST00000302053
Start 154584746:154584747(version: GRCh38)
Mutation Type INS
dbSNP_RS rs757027534
CDS Mutation c.1978dupT
AA Mutation p.Ser660PhefsTer27(p.S660Ffs*27)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 23
Mutation Consequence frameshift_variant
Transcription ID ENST00000302053
Start 154588854:154588855(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.302_303insAA
AA Mutation p.Asp101GlufsTer6(p.D101Efs*6)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 24
Mutation Consequence protein_altering_variant
Transcription ID ENST00000302053
Start 154587648:154587649(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.373_374insCTTACCTCCAGTCGTTTC
AA Mutation p.Asn125delinsThrTyrLeuGlnSerPheHis(p.N125delinsTYLQSFH)
Mutation Classification In_Frame_Ins
Feature Type Transcript

Rectum Cancer: Gene >> FGA

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154584155:154584155(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2570G>A
AA Mutation p.Arg857His(p.R857H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154587594:154587594(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750761333
CDS Mutation c.428G>A
AA Mutation p.Arg143His(p.R143H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154586258:154586258(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1171G>A
AA Mutation p.Gly391Arg(p.G391R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154586326:154586326(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1103G>T
AA Mutation p.Gly368Val(p.G368V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154585973:154585973(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1456G>A
AA Mutation p.Glu486Lys(p.E486K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154586330:154586330(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1099C>T
AA Mutation p.Arg367Cys(p.R367C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154585868:154585868(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755603154
CDS Mutation c.1561G>A
AA Mutation p.Asp521Asn(p.D521N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000302053
Start 154588852:154588852(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.305C>A
AA Mutation p.Ser102Tyr(p.S102Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000302053
Start 154584609:154584609(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2116G>T
AA Mutation p.Glu706Ter(p.E706*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript