Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GOLGA4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37327484:37327484(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5598G>T
AA Mutation p.Gln1866His(p.Q1866H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37324433:37324433(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2547G>T
AA Mutation p.Lys849Asn(p.K849N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37326494:37326494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4608G>T
AA Mutation p.Gln1536His(p.Q1536H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37298894:37298894(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.876G>T
AA Mutation p.Glu292Asp(p.E292D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37326367:37326367(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201034947
CDS Mutation c.4481G>T
AA Mutation p.Arg1494Ile(p.R1494I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37329062:37329062(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6161G>A
AA Mutation p.Arg2054Gln(p.R2054Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37282025:37282025(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768808136
CDS Mutation c.230G>A
AA Mutation p.Arg77Gln(p.R77Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37298886:37298886(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.868C>A
AA Mutation p.Arg290Ser(p.R290S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37325788:37325788(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3902A>C
AA Mutation p.Glu1301Ala(p.E1301A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37243564:37243564(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.14T>C
AA Mutation p.Leu5Pro(p.L5P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37282079:37282079(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372845682
CDS Mutation c.284G>A
AA Mutation p.Arg95Gln(p.R95Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37321851:37321851(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs113898889
CDS Mutation c.1666C>T
AA Mutation p.Arg556Trp(p.R556W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37326348:37326348(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4462C>A
AA Mutation p.Leu1488Ile(p.L1488I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37315479:37315479(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1294A>G
AA Mutation p.Lys432Glu(p.K432E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37325453:37325453(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3567A>C
AA Mutation p.Lys1189Asn(p.K1189N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37326057:37326057(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764030527
CDS Mutation c.4171G>A
AA Mutation p.Glu1391Lys(p.E1391K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37327456:37327456(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5570A>G
AA Mutation p.Lys1857Arg(p.K1857R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37282226:37282226(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778956577
CDS Mutation c.431G>A
AA Mutation p.Arg144Gln(p.R144Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37337682:37337682(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6344A>C
AA Mutation p.Lys2115Thr(p.K2115T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37282171:37282171(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.376G>T
AA Mutation p.Asp126Tyr(p.D126Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37323797:37323797(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1911A>C
AA Mutation p.Gln637His(p.Q637H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37326705:37326705(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4819G>A
AA Mutation p.Glu1607Lys(p.E1607K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37315473:37315473(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373660326
CDS Mutation c.1288C>T
AA Mutation p.Arg430Trp(p.R430W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37324027:37324027(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2141C>A
AA Mutation p.Thr714Lys(p.T714K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37327398:37327398(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749363115
CDS Mutation c.5512G>A
AA Mutation p.Val1838Ile(p.V1838I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000361924
Start 37337704:37337704(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6366G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000361924
Start 37324115:37324115(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2229C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000361924
Start 37302250:37302250(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749789355
CDS Mutation c.1152T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000361924
Start 37361269:37361269(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6690C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000361924
Start 37326674:37326674(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4788C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence frameshift_variant
Transcription ID ENST00000361924
Start 37315519:37315519(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1339delA
AA Mutation p.Thr447GlnfsTer13(p.T447Qfs*13)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 32
Mutation Consequence frameshift_variant
Transcription ID ENST00000361924
Start 37327294:37327294(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5414delA
AA Mutation p.Asn1805ThrfsTer6(p.N1805Tfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 33
Mutation Consequence frameshift_variant
Transcription ID ENST00000361924
Start 37315456:37315456(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1276delA
AA Mutation p.Thr426GlnfsTer8(p.T426Qfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 34
Mutation Consequence stop_gained
Transcription ID ENST00000361924
Start 37326567:37326567(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4681G>T
AA Mutation p.Glu1561Ter(p.E1561*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence stop_gained
Transcription ID ENST00000361924
Start 37326594:37326594(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4708C>T
AA Mutation p.Gln1570Ter(p.Q1570*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence stop_gained
Transcription ID ENST00000361924
Start 37326270:37326270(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4384G>T
AA Mutation p.Glu1462Ter(p.E1462*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence stop_gained
Transcription ID ENST00000361924
Start 37326705:37326705(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4819G>T
AA Mutation p.Glu1607Ter(p.E1607*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence frameshift_variant
Transcription ID ENST00000361924
Start 37327293:37327294(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.5414dupA
AA Mutation p.Asn1805LysfsTer18(p.N1805Kfs*18)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> GOLGA4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37326167:37326167(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4281G>T
AA Mutation p.Glu1427Asp(p.E1427D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37296171:37296171(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.766G>A
AA Mutation p.Glu256Lys(p.E256K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37327395:37327395(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148910546
CDS Mutation c.5509G>A
AA Mutation p.Asp1837Asn(p.D1837N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37325559:37325559(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3673G>A
AA Mutation p.Glu1225Lys(p.E1225K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37326494:37326494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4608G>T
AA Mutation p.Gln1536His(p.Q1536H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37326743:37326743(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4857G>T
AA Mutation p.Glu1619Asp(p.E1619D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37326841:37326841(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4955A>C
AA Mutation p.Lys1652Thr(p.K1652T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37327800:37327800(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5914G>T
AA Mutation p.Asp1972Tyr(p.D1972Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37282208:37282208(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.413A>C
AA Mutation p.Gln138Pro(p.Q138P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000361924
Start 37289289:37289289(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.580G>A
AA Mutation p.Glu194Lys(p.E194K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000361924
Start 37315474:37315474(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1289G>A
AA Mutation p.Arg430Gln(p.R430Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000361924
Start 37326272:37326272(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4386A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000361924
Start 37326567:37326567(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4681G>T
AA Mutation p.Glu1561Ter(p.E1561*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript