Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ZBTB18

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000622512
Start 244054261:244054261(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756323931
CDS Mutation c.460G>A
AA Mutation p.Asp154Asn(p.D154N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000622512
Start 244054270:244054270(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.469A>T
AA Mutation p.Ser157Cys(p.S157C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000622512
Start 244054897:244054897(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371575631
CDS Mutation c.1096G>A
AA Mutation p.Ala366Thr(p.A366T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000622512
Start 244054930:244054930(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1129A>G
AA Mutation p.Lys377Glu(p.K377E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000622512
Start 244055034:244055034(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373253112
CDS Mutation c.1233G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000622512
Start 244054357:244054357(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.556C>T
AA Mutation p.Arg186Ter(p.R186*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> ZBTB18

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000622512
Start 244054499:244054499(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768000553
CDS Mutation c.698C>T
AA Mutation p.Ser233Leu(p.S233L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence stop_gained
Transcription ID ENST00000622512
Start 244054357:244054357(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.556C>T
AA Mutation p.Arg186Ter(p.R186*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript