Mutation

Primary Site >> Stomach Cancer

Gene >> ALPK2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58537543:58537543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574202609
CDS Mutation	c.2644G>A
AA Mutation	p.Gly882Ser(p.G882S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58481987:58481987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6349G>T
AA Mutation	p.Ala2117Ser(p.A2117S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58536672:58536672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140868694
CDS Mutation	c.3515C>T
AA Mutation	p.Thr1172Met(p.T1172M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58536205:58536205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3982C>A
AA Mutation	p.Leu1328Ile(p.L1328I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58516973:58516973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375621243
CDS Mutation	c.5875G>A
AA Mutation	p.Ala1959Thr(p.A1959T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58535538:58535538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4649A>G
AA Mutation	p.His1550Arg(p.H1550R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58578827:58578827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1949G>T
AA Mutation	p.Ser650Ile(p.S650I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58537384:58537384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2803A>G
AA Mutation	p.Ser935Gly(p.S935G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58503982:58503982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6196C>T
AA Mutation	p.His2066Tyr(p.H2066Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58537669:58537669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2518A>G
AA Mutation	p.Thr840Ala(p.T840A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58535686:58535686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748622515
CDS Mutation	c.4501G>A
AA Mutation	p.Gly1501Ser(p.G1501S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58579515:58579515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150536488
CDS Mutation	c.1261G>A
AA Mutation	p.Gly421Ser(p.G421S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58579337:58579337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1439C>T
AA Mutation	p.Ala480Val(p.A480V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58536631:58536631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139032503
CDS Mutation	c.3556C>T
AA Mutation	p.Arg1186Cys(p.R1186C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58579778:58579778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998C>T
AA Mutation	p.Ser333Phe(p.S333F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58504060:58504060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6118T>C
AA Mutation	p.Tyr2040His(p.Y2040H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58517089:58517089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372914995
CDS Mutation	c.5759C>T
AA Mutation	p.Thr1920Met(p.T1920M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000361673
Start	58537869:58537869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2318C>T
AA Mutation	p.Ala773Val(p.A773V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361673
Start	58537589:58537589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2598A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361673
Start	58537484:58537484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2703A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361673
Start	58504051:58504051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6127A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361673
Start	58536218:58536218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3969A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361673
Start	58579096:58579096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1680T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361673
Start	58579208:58579208(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1568delA
AA Mutation	p.Lys523ArgfsTer15(p.K523Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361673
Start	58579709:58579709(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1067delT
AA Mutation	p.Leu356TyrfsTer2(p.L356Yfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361673
Start	58611766:58611766(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.32delC
AA Mutation	p.Pro11ArgfsTer24(p.P11Rfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript