Primary Site >> Liver Cancer

Gene >> A2M

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9112526:9112526(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749221334
CDS Mutation c.281C>T
AA Mutation p.Ser94Phe(p.S94F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9077824:9077824(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3153A>C
AA Mutation p.Gln1051His(p.Q1051H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9095661:9095661(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1891C>A
AA Mutation p.Pro631Thr(p.P631T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9068792:9068792(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4314A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9106239:9106239(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1101G>A
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9110323:9110323(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.495A>G
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID ENST00000318602
Start 9074776:9074788(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3533-5_3540delTTAAGACAACTCT
Mutation Classification Splice_Site
Feature Type Transcript