Primary Site >> Stomach Cancer

Gene >> CLASRP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000221455
Start 45070542:45070542(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1963G>A
AA Mutation p.Glu655Lys(p.E655K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000221455
Start 45070558:45070558(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1979G>A
AA Mutation p.Arg660Gln(p.R660Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000221455
Start 45057797:45057797(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752674221
CDS Mutation c.512C>T
AA Mutation p.Thr171Met(p.T171M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000221455
Start 45070823:45070823(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755598805
CDS Mutation c.2003G>A
AA Mutation p.Arg668Gln(p.R668Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000221455
Start 45060581:45060581(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.817G>A
AA Mutation p.Glu273Lys(p.E273K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000221455
Start 45070083:45070083(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753553785
CDS Mutation c.1936C>T
AA Mutation p.Arg646Cys(p.R646C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000221455
Start 45052841:45052841(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.248G>A
AA Mutation p.Arg83His(p.R83H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000221455
Start 45070064:45070064(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1917C>T
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000221455
Start 45067580:45067580(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1653C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000221455
Start 45052871:45052871(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.284delC
AA Mutation p.Pro95LeufsTer81(p.P95Lfs*81)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 11
Mutation Consequence splice_donor_variant
Transcription ID ENST00000221455
Start 45040312:45040312(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.99+1G>A
Mutation Classification Splice_Site
Feature Type Transcript