Primary Site >> Stomach Cancer

Gene >> KARS

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000302445
Start 75629473:75629473(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1493C>T
AA Mutation p.Ala498Val(p.A498V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000302445
Start 75634198:75634198(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.890G>T
AA Mutation p.Arg297Ile(p.R297I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000302445
Start 75635793:75635793(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs574836321
CDS Mutation c.682C>T
AA Mutation p.Arg228Cys(p.R228C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000302445
Start 75636052:75636052(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.529C>T
AA Mutation p.Arg177Cys(p.R177C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000302445
Start 75631812:75631812(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs527981017
CDS Mutation c.959G>A
AA Mutation p.Arg320His(p.R320H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000302445
Start 75635981:75635981(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143003475
CDS Mutation c.600G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000302445
Start 75631498:75631498(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1170C>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000302445
Start 75636482:75636482(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.454delG
AA Mutation p.Val152Ter(p.V152*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence stop_gained;frameshift_variant
Transcription ID ENST00000302445
Start 75636087:75636088(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.487_493dupTATAAAT
AA Mutation p.Ser165LeufsTer2(p.S165Lfs*2)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000302445
Start 75636028:75636028(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.553C>T
AA Mutation p.Gln185Ter(p.Q185*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript