Mutation

Primary Site >> Liver Cancer

Gene >> SDK1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	3969286:3969286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753638529
CDS Mutation	c.1576C>T
AA Mutation	p.Arg526Trp(p.R526W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	4205960:4205960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548946940
CDS Mutation	c.5180C>T
AA Mutation	p.Pro1727Leu(p.P1727L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	4017290:4017290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2540C>G
AA Mutation	p.Ala847Gly(p.A847G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	4051800:4051800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2881A>T
AA Mutation	p.Thr961Ser(p.T961S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	3958999:3958999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780085119
CDS Mutation	c.1219G>A
AA Mutation	p.Gly407Arg(p.G407R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	3639048:3639048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143792155
CDS Mutation	c.503G>A
AA Mutation	p.Arg168His(p.R168H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	4245713:4245713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6289T>C
AA Mutation	p.Ser2097Pro(p.S2097P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000404826
Start	4210162:4210162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5539G>C
AA Mutation	p.Gly1847Arg(p.G1847R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	4237761:4237761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6107A>G
AA Mutation	p.Lys2036Arg(p.K2036R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	3619175:3619175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394T>C
AA Mutation	p.Trp132Arg(p.W132R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	4051717:4051717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2798G>A
AA Mutation	p.Gly933Glu(p.G933E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	3969412:3969412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702C>T
AA Mutation	p.Leu568Phe(p.L568F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	4205887:4205887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5107A>G
AA Mutation	p.Met1703Val(p.M1703V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	3974509:3974509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1958G>C
AA Mutation	p.Gly653Ala(p.G653A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	3619233:3619233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762716721
CDS Mutation	c.452A>T
AA Mutation	p.Glu151Val(p.E151V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	4114101:4114101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3650G>A
AA Mutation	p.Arg1217His(p.R1217H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	4110697:4110697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3359C>T
AA Mutation	p.Thr1120Ile(p.T1120I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	4149286:4149286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4448T>A
AA Mutation	p.Leu1483His(p.L1483H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000404826
Start	3958988:3958988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1208C>T
AA Mutation	p.Thr403Ile(p.T403I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404826
Start	3974489:3974489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1938C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404826
Start	4161790:4161790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4734A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000404826
Start	4113373:4113373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3519C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000404826
Start	3619078:3619078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299-2A>T
Mutation Classification	Splice_Site
Feature Type	Transcript