Primary Site >> Stomach Cancer

Gene >> NDC80

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000261597
Start 2578059:2578059(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.394C>A
AA Mutation p.Leu132Ile(p.L132I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000261597
Start 2577823:2577823(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.257T>G
AA Mutation p.Leu86Arg(p.L86R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000261597
Start 2595495:2595495(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1095C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000261597
Start 2575052:2575052(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369863089
CDS Mutation c.165G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000261597
Start 2578996:2578996(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.546G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000261597
Start 2601453:2601453(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1438delA
AA Mutation p.Met480TrpfsTer7(p.M480Wfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript