Primary Site >> Liver Cancer

Gene >> MLH3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000355774
Start 75038385:75038385(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3598A>G
AA Mutation p.Ile1200Val(p.I1200V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000355774
Start 75033433:75033433(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3701A>T
AA Mutation p.Glu1234Val(p.E1234V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000355774
Start 75047504:75047504(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2152C>G
AA Mutation p.Pro718Ala(p.P718A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000355774
Start 75048767:75048767(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775001669
CDS Mutation c.889C>T
AA Mutation p.Arg297Trp(p.R297W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000355774
Start 75049619:75049619(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.37T>C
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000355774
Start 75018957:75018975(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4096_4114delATTAAGTTTAATGATGGCC
AA Mutation p.Ile1366Ter(p.I1366*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000355774
Start 75046669:75046669(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2987delG
AA Mutation p.Gly996GlufsTer10(p.G996Efs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript