Primary Site >> Stomach Cancer

Gene >> KLRC1

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000359151
Start 10449238:10449238(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771654012
CDS Mutation c.488T>C
AA Mutation p.Met163Thr(p.M163T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359151
Start 10449271:10449271(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.455C>A
AA Mutation p.Ser152Tyr(p.S152Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359151
Start 10451131:10451131(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.26C>T
AA Mutation p.Ser9Leu(p.S9L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359151
Start 10451116:10451116(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757144280
CDS Mutation c.41C>T
AA Mutation p.Pro14Leu(p.P14L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000359151
Start 10451034:10451034(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs562831230
CDS Mutation c.123G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000359151
Start 10449375:10449375(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.351C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000359151
Start 10451113:10451113(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.44delC
AA Mutation p.Pro15GlnfsTer18(p.P15Qfs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript