Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZNF77

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000314531
Start 2933856:2933856(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770910866
CDS Mutation c.1271G>A
AA Mutation p.Arg424Gln(p.R424Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000314531
Start 2933623:2933623(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1504A>C
AA Mutation p.Ser502Arg(p.S502R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000314531
Start 2934235:2934235(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.892T>A
AA Mutation p.Cys298Ser(p.C298S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000314531
Start 2934032:2934032(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1095C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000314531
Start 2933594:2933594(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1533G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000314531
Start 2933492:2933492(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs76980806
CDS Mutation c.1635G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000314531
Start 2936658:2936658(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770342384
CDS Mutation c.177C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000314531
Start 2933761:2933761(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768214682
CDS Mutation c.1366C>T
AA Mutation p.Arg456Ter(p.R456*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> ZNF77

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000314531
Start 2933871:2933871(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1256T>G
AA Mutation p.Phe419Cys(p.F419C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000314531
Start 2934715:2934715(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.412G>A
AA Mutation p.Glu138Lys(p.E138K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000314531
Start 2936572:2936572(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.263G>T
AA Mutation p.Arg88Ile(p.R88I)
Mutation Classification Missense_Mutation
Feature Type Transcript