Primary Site >> Stomach Cancer

Gene >> CALB2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302628
Start 71374803:71374803(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.230A>C
AA Mutation p.Lys77Thr(p.K77T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302628
Start 71389842:71389842(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767492769
CDS Mutation c.793C>T
AA Mutation p.Leu265Phe(p.L265F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302628
Start 71374815:71374815(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.242G>T
AA Mutation p.Gly81Val(p.G81V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302628
Start 71389773:71389773(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.724A>G
AA Mutation p.Asn242Asp(p.N242D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000302628
Start 71377735:71377735(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146835226
CDS Mutation c.330C>T
Mutation Classification Silent
Feature Type Transcript