Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> G3BP1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151799965:151799965(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775783436
CDS Mutation c.920G>A
AA Mutation p.Arg307Gln(p.R307Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151794192:151794192(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.385G>T
AA Mutation p.Asp129Tyr(p.D129Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151799932:151799932(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.887G>T
AA Mutation p.Arg296Ile(p.R296I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151790944:151790944(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370340219
CDS Mutation c.233G>A
AA Mutation p.Arg78His(p.R78H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151803970:151803970(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1280G>A
AA Mutation p.Arg427His(p.R427H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151791055:151791055(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.344C>T
AA Mutation p.Ala115Val(p.A115V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151804083:151804083(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372751446
CDS Mutation c.1393C>T
AA Mutation p.Arg465Trp(p.R465W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151800784:151800784(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765135383
CDS Mutation c.1109G>A
AA Mutation p.Arg370His(p.R370H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151795499:151795499(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.463G>A
AA Mutation p.Glu155Lys(p.E155K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151794175:151794175(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.368A>C
AA Mutation p.Lys123Thr(p.K123T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151804029:151804029(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs187250945
CDS Mutation c.1339C>T
AA Mutation p.Arg447Cys(p.R447C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151800763:151800763(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1088A>G
AA Mutation p.Tyr363Cys(p.Y363C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151795524:151795524(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.488C>A
AA Mutation p.Pro163His(p.P163H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151790335:151790335(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.108G>T
AA Mutation p.Lys36Asn(p.K36N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000356245
Start 151790966:151790966(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200897287
CDS Mutation c.255G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000356245
Start 151786638:151786638(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.18T>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000356245
Start 151790395:151790395(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373179919
CDS Mutation c.168C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence splice_donor_variant
Transcription ID ENST00000356245
Start 151800001:151800001(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.955+1G>A
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 19
Mutation Consequence start_lost
Transcription ID ENST00000356245
Start 151786621:151786621(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1A>G
AA Mutation p.Met1?(p.M1?)
Mutation Classification Translation_Start_Site
Feature Type Transcript

Rectum Cancer: Gene >> G3BP1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000356245
Start 151799965:151799965(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775783436
CDS Mutation c.920G>A
AA Mutation p.Arg307Gln(p.R307Q)
Mutation Classification Missense_Mutation
Feature Type Transcript