Mutation

Primary Site >> Stomach Cancer

Gene >> ALPK3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84857763:84857763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765812547
CDS Mutation	c.3631C>T
AA Mutation	p.Arg1211Trp(p.R1211W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84839818:84839818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs574988897
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382His(p.R382H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84839919:84839919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1246C>T
AA Mutation	p.Arg416Cys(p.R416C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84862823:84862823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4924C>A
AA Mutation	p.Arg1642Ser(p.R1642S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84859353:84859353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4534G>A
AA Mutation	p.Ala1512Thr(p.A1512T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84862767:84862767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770717324
CDS Mutation	c.4868G>A
AA Mutation	p.Arg1623Gln(p.R1623Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84840679:84840679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2006C>T
AA Mutation	p.Thr669Ile(p.T669I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84867332:84867332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5345T>A
AA Mutation	p.Met1782Lys(p.M1782K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84840295:84840295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1622G>A
AA Mutation	p.Arg541His(p.R541H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84839030:84839030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766905744
CDS Mutation	c.961C>T
AA Mutation	p.Arg321Cys(p.R321C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84857704:84857704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3572G>A
AA Mutation	p.Gly1191Glu(p.G1191E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84840601:84840601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1928C>T
AA Mutation	p.Ala643Val(p.A643V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84839866:84839866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1193T>G
AA Mutation	p.Ile398Ser(p.I398S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84868280:84868280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5548A>G
AA Mutation	p.Lys1850Glu(p.K1850E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84839793:84839793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1120A>T
AA Mutation	p.Met374Leu(p.M374L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84827531:84827531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372130536
CDS Mutation	c.836C>T
AA Mutation	p.Pro279Leu(p.P279L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84840405:84840405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1732C>T
AA Mutation	p.Arg578Trp(p.R578W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000258888
Start	84857250:84857250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3118T>C
AA Mutation	p.Cys1040Arg(p.C1040R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258888
Start	84857246:84857246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3114C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258888
Start	84840449:84840449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1776C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258888
Start	84856655:84856655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141003674
CDS Mutation	c.2523G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258888
Start	84862759:84862759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4860T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258888
Start	84840018:84840018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1345C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258888
Start	84864620:84864620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5284C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258888
Start	84840110:84840110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1437C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258888
Start	84868348:84868348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5616T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258888
Start	84857150:84857150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370157683
CDS Mutation	c.3018G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258888
Start	84857036:84857036(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2910delA
AA Mutation	p.Lys970AsnfsTer12(p.K970Nfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258888
Start	84857271:84857271(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3143delG
AA Mutation	p.Gly1048GlufsTer12(p.G1048Efs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000258888
Start	84839868:84839868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1195G>T
AA Mutation	p.Glu399Ter(p.E399*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000258888
Start	84857035:84857036(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2910dupA
AA Mutation	p.Pro971ThrfsTer8(p.P971Tfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript