Primary Site >> Liver Cancer

Gene >> ITGA9

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264741
Start 37533320:37533320(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1380G>T
AA Mutation p.Arg460Ser(p.R460S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264741
Start 37533393:37533393(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369791724
CDS Mutation c.1453G>A
AA Mutation p.Gly485Arg(p.G485R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264741
Start 37653736:37653736(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779583800
CDS Mutation c.1862G>A
AA Mutation p.Arg621His(p.R621H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000264741
Start 37779937:37779937(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2703A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000264741
Start 37629207:37629207(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs145334938
CDS Mutation c.1710C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000264741
Start 37732789:37732789(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2145A>C
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000264741
Start 37542457:37542457(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1565delA
AA Mutation p.Lys522ArgfsTer27(p.K522Rfs*27)
Mutation Classification Frame_Shift_Del
Feature Type Transcript