Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MZF1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000215057
Start 58563499:58563499(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777893427
CDS Mutation c.778G>A
AA Mutation p.Ala260Thr(p.A260T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000215057
Start 58563207:58563207(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1070G>A
AA Mutation p.Arg357His(p.R357H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000215057
Start 58563264:58563264(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1013C>A
AA Mutation p.Pro338His(p.P338H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000215057
Start 58563441:58563441(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.836T>C
AA Mutation p.Val279Ala(p.V279A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000215057
Start 58562121:58562121(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2156A>G
AA Mutation p.His719Arg(p.H719R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000215057
Start 58563106:58563106(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1171C>T
AA Mutation p.Arg391Cys(p.R391C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000215057
Start 58562139:58562139(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2138A>G
AA Mutation p.Asp713Gly(p.D713G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000215057
Start 58562509:58562509(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1768G>A
AA Mutation p.Val590Ile(p.V590I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000215057
Start 58562564:58562564(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1713C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000215057
Start 58563203:58563203(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1074C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000215057
Start 58571150:58571150(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.240G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000215057
Start 58571108:58571108(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374998042
CDS Mutation c.282C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000215057
Start 58562218:58562219(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.2058_2059delTG
AA Mutation p.Cys686TrpfsTer70(p.C686Wfs*70)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000215057
Start 58570360:58570361(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.563_564delAG
AA Mutation p.Glu188GlyfsTer26(p.E188Gfs*26)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> MZF1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000215057
Start 58569575:58569575(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.592T>G
AA Mutation p.Ser198Ala(p.S198A)
Mutation Classification Missense_Mutation
Feature Type Transcript