Primary Site >> Stomach Cancer

Gene >> CARD10

ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000251973
Start 37507831:37507831(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1189C>G
AA Mutation p.Gln397Glu(p.Q397E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000251973
Start 37518049:37518049(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.295G>C
AA Mutation p.Ala99Pro(p.A99P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000251973
Start 37518030:37518030(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.314C>A
AA Mutation p.Pro105His(p.P105H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000251973
Start 37518009:37518009(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.335C>T
AA Mutation p.Thr112Met(p.T112M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000251973
Start 37516106:37516106(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.566G>A
AA Mutation p.Arg189Gln(p.R189Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000251973
Start 37518105:37518105(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772945473
CDS Mutation c.239G>A
AA Mutation p.Arg80His(p.R80H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000251973
Start 37516246:37516246(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.426G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000251973
Start 37497143:37497143(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1823delC
AA Mutation p.Pro608GlnfsTer75(p.P608Qfs*75)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence inframe_insertion
Transcription ID ENST00000251973
Start 37497023:37497024(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1937_1942dupAACCAA
AA Mutation p.Pro647_Arg648insLysPro(p.P647_R648insKP)
Mutation Classification In_Frame_Ins
Feature Type Transcript