Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GRIA2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157361026:157361026(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2308G>A
AA Mutation p.Ala770Thr(p.A770T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157334085:157334085(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1231C>T
AA Mutation p.Leu411Phe(p.L411F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157303681:157303681(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.359G>C
AA Mutation p.Gly120Ala(p.G120A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157341454:157341454(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2035T>A
AA Mutation p.Phe679Ile(p.F679I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157312765:157312765(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.556G>T
AA Mutation p.Asp186Tyr(p.D186Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157360070:157360070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2218G>A
AA Mutation p.Asp740Asn(p.D740N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157336518:157336518(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1615C>A
AA Mutation p.Leu539Ile(p.L539I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157303762:157303762(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.440A>C
AA Mutation p.Lys147Thr(p.K147T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157332931:157332931(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.995C>A
AA Mutation p.Ala332Glu(p.A332E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157335837:157335837(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778623018
CDS Mutation c.1433C>T
AA Mutation p.Thr478Met(p.T478M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157332940:157332940(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1004C>A
AA Mutation p.Ala335Glu(p.A335E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157336704:157336704(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1801T>C
AA Mutation p.Ser601Pro(p.S601P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157336705:157336705(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1802C>A
AA Mutation p.Ser601Tyr(p.S601Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157303606:157303606(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.284A>C
AA Mutation p.Lys95Thr(p.K95T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157333255:157333255(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1057G>A
AA Mutation p.Val353Ile(p.V353I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157312822:157312822(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200369612
CDS Mutation c.613C>T
AA Mutation p.Arg205Trp(p.R205W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157341278:157341278(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1859G>A
AA Mutation p.Arg620His(p.R620H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157359995:157359995(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2143C>T
AA Mutation p.Arg715Trp(p.R715W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157303617:157303617(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.295A>G
AA Mutation p.Thr99Ala(p.T99A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157221792:157221792(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.214G>A
AA Mutation p.Ala72Thr(p.A72T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157362926:157362926(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752525141
CDS Mutation c.2534G>A
AA Mutation p.Arg845Gln(p.R845Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157336495:157336495(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1592C>A
AA Mutation p.Ser531Tyr(p.S531Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157335725:157335725(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761885028
CDS Mutation c.1321C>T
AA Mutation p.Arg441Cys(p.R441C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157360035:157360035(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2183C>T
AA Mutation p.Thr728Met(p.T728M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157360027:157360027(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2175G>T
AA Mutation p.Leu725Phe(p.L725F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157341321:157341321(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1902C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157362915:157362915(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759531543
CDS Mutation c.2523C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157221686:157221686(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.108C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157336613:157336613(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs538981621
CDS Mutation c.1710C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157341270:157341270(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1851C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157335748:157335748(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1344C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157360036:157360036(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760253405
CDS Mutation c.2184G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157359976:157359976(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143272523
CDS Mutation c.2124C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157335838:157335838(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745408425
CDS Mutation c.1434G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157221791:157221791(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746340381
CDS Mutation c.213C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157312786:157312786(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.577C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157333287:157333287(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1089C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence frameshift_variant
Transcription ID ENST00000264426
Start 157336555:157336555(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1656delT
AA Mutation p.Phe552LeufsTer8(p.F552Lfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 39
Mutation Consequence frameshift_variant
Transcription ID ENST00000264426
Start 157321572:157321572(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.857delC
AA Mutation p.Pro286LeufsTer14(p.P286Lfs*14)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 40
Mutation Consequence stop_gained
Transcription ID ENST00000264426
Start 157221711:157221711(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.133C>T
AA Mutation p.Arg45Ter(p.R45*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000264426
Start 157221666:157221666(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.93delG
AA Mutation p.Leu32TyrfsTer15(p.X31_splice)
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> GRIA2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157334039:157334039(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1185G>T
AA Mutation p.Met395Ile(p.M395I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157332939:157332939(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1003G>C
AA Mutation p.Ala335Pro(p.A335P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157362838:157362838(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2446G>A
AA Mutation p.Val816Ile(p.V816I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157362883:157362883(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2491G>A
AA Mutation p.Ala831Thr(p.A831T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157221731:157221731(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.153T>G
AA Mutation p.Phe51Leu(p.F51L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157335870:157335870(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1466T>C
AA Mutation p.Val489Ala(p.V489A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157336597:157336597(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1694G>T
AA Mutation p.Ser565Ile(p.S565I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157312751:157312751(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.542G>A
AA Mutation p.Gly181Glu(p.G181E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157341277:157341277(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759660118
CDS Mutation c.1858C>T
AA Mutation p.Arg620Cys(p.R620C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157341456:157341456(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2037T>G
AA Mutation p.Phe679Leu(p.F679L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157360070:157360070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2218G>A
AA Mutation p.Asp740Asn(p.D740N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000264426
Start 157362862:157362862(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2470C>A
AA Mutation p.Leu824Ile(p.L824I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157336613:157336613(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs538981621
CDS Mutation c.1710C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157359976:157359976(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143272523
CDS Mutation c.2124C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000264426
Start 157317663:157317663(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.672T>C
Mutation Classification Silent
Feature Type Transcript