Mutation

Primary Site >> Liver Cancer

Gene >> PPP2R5D

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000485511
Start	43008002:43008002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.794T>C
AA Mutation	p.Ile265Thr(p.I265T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000485511
Start	43011224:43011224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1747A>C
AA Mutation	p.Lys583Gln(p.K583Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000485511
Start	42989614:42989614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.31C>T
AA Mutation	p.Pro11Ser(p.P11S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000485511
Start	42989663:42989663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80A>G
AA Mutation	p.Asp27Gly(p.D27G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000485511
Start	43008210:43008210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759229882
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000485511
Start	43008036:43008036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000485511
Start	43010655:43010736(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1482-8_1554+1delCTCCTCAGGGGCCGGTTCCGAATGAAGGAAAGGGAAGAGATGTGGCAAAAAATCGAGGAGCTGGCCCGGCTTAATCCCCAGG
Mutation Classification	Splice_Site
Feature Type	Transcript