Mutation

Primary Site >> Liver Cancer

Gene >> STAB2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000388887
Start	103666336:103666336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147674384
CDS Mutation	c.2068G>A
AA Mutation	p.Ala690Thr(p.A690T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000388887
Start	103761304:103761304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7253A>C
AA Mutation	p.Glu2418Ala(p.E2418A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000388887
Start	103755426:103755426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6839A>G
AA Mutation	p.Asn2280Ser(p.N2280S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000388887
Start	103654598:103654598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752616430
CDS Mutation	c.1451T>C
AA Mutation	p.Val484Ala(p.V484A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000388887
Start	103662946:103662946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1970T>C
AA Mutation	p.Ile657Thr(p.I657T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000388887
Start	103755454:103755454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6867C>G
AA Mutation	p.Cys2289Trp(p.C2289W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388887
Start	103713707:103713707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4476C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388887
Start	103742409:103742409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747762448
CDS Mutation	c.5886C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388887
Start	103706806:103706806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755755156
CDS Mutation	c.4011T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388887
Start	103725079:103725079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751986200
CDS Mutation	c.4788C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388887
Start	103683282:103683282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2883C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000388887
Start	103673944:103673944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2409A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000388887
Start	103742550:103742550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6027T>A
AA Mutation	p.Cys2009Ter(p.C2009*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000388887
Start	103763491:103763491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7489-1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000388887
Start	103677451:103677451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2647-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript