Primary Site >> Stomach Cancer

Gene >> MYLK3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000394809
Start 46712751:46712751(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2011G>C
AA Mutation p.Val671Leu(p.V671L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000394809
Start 46747824:46747824(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147831842
CDS Mutation c.370G>A
AA Mutation p.Ala124Thr(p.A124T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000394809
Start 46727355:46727355(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780286175
CDS Mutation c.1795G>A
AA Mutation p.Asp599Asn(p.D599N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000394809
Start 46732309:46732309(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1361G>A
AA Mutation p.Gly454Glu(p.G454E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000394809
Start 46727236:46727236(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1914G>T
AA Mutation p.Lys638Asn(p.K638N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000394809
Start 46729606:46729606(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1650C>T
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000394809
Start 46732269:46732269(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1401G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000394809
Start 46721195:46721195(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1915-2delA
Mutation Classification Splice_Site
Feature Type Transcript