Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NUDT18

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000611621
Start 22107613:22107613(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375524530
CDS Mutation c.659G>A
AA Mutation p.Gly220Asp(p.G220D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000611621
Start 22107472:22107472(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.800G>A
AA Mutation p.Gly267Asp(p.G267D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000611621
Start 22107663:22107663(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.609G>T
AA Mutation p.Trp203Cys(p.W203C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000611621
Start 22107344:22107344(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.928C>T
AA Mutation p.Leu310Phe(p.L310F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000611621
Start 22108339:22108339(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.170T>C
AA Mutation p.Val57Ala(p.V57A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000611621
Start 22108329:22108329(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.180C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000611621
Start 22107450:22107450(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.822G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000611621
Start 22108302:22108302(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.207delG
AA Mutation p.Ser70ArgfsTer23(p.S70Rfs*23)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> NUDT18

No Mutation Annotation!