Primary Site >> Pancreatic Cancer

Gene >> LAMA3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000313654
Start 23827387:23827387(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2743C>G
AA Mutation p.Leu915Val(p.L915V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000313654
Start 23916644:23916644(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7872G>T
AA Mutation p.Gln2624His(p.Q2624H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000313654
Start 23914478:23914478(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7398C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000313654
Start 23949809:23949809(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9396G>A
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000313654
Start 23939282:23939282(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8922C>A
AA Mutation p.Cys2974Ter(p.C2974*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000313654
Start 23864857:23864858(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.4661dupA
AA Mutation p.Lys1555GlufsTer16(p.K1555Efs*16)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 7
Mutation Consequence inframe_insertion
Transcription ID ENST00000313654
Start 23827385:23827386(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2741_2742insTAGGGTTAGGGTTAGGGTTAGGGTTAGGGTTAG
AA Mutation p.Leu914_Leu915insArgValArgValArgValArgValArgValArg(p.L914_L915insRVRVRVRVRVR)
Mutation Classification In_Frame_Ins
Feature Type Transcript