Mutation

Primary Site >> Stomach Cancer

Gene >> ALPK1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000177648
Start	112430941:112430941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202180512
CDS Mutation	c.1394C>T
AA Mutation	p.Ser465Leu(p.S465L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000177648
Start	112429212:112429212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753593541
CDS Mutation	c.859G>A
AA Mutation	p.Ala287Thr(p.A287T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000177648
Start	112382451:112382451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.175T>C
AA Mutation	p.Trp59Arg(p.W59R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000177648
Start	112430668:112430668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772519624
CDS Mutation	c.1121C>T
AA Mutation	p.Thr374Met(p.T374M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000177648
Start	112440931:112440931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3553A>G
AA Mutation	p.Asn1185Asp(p.N1185D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000177648
Start	112382460:112382460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188866014
CDS Mutation	c.184G>A
AA Mutation	p.Val62Met(p.V62M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000177648
Start	112432417:112432417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2870C>T
AA Mutation	p.Ser957Phe(p.S957F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000177648
Start	112435177:112435177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3064T>A
AA Mutation	p.Ser1022Thr(p.S1022T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000177648
Start	112411972:112411972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422C>T
AA Mutation	p.Thr141Met(p.T141M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000177648
Start	112411941:112411941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391G>A
AA Mutation	p.Ala131Thr(p.A131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000177648
Start	112431812:112431812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375743965
CDS Mutation	c.2265C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000177648
Start	112411964:112411964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.414G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000177648
Start	112430858:112430858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145906942
CDS Mutation	c.1311C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000177648
Start	112432511:112432511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2964G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000177648
Start	112432253:112432253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76049625
CDS Mutation	c.2706C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000177648
Start	112432262:112432262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2715C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000177648
Start	112431014:112431014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1467C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000177648
Start	112432559:112432559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772371704
CDS Mutation	c.3012C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000177648
Start	112435170:112435170(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3063delA
AA Mutation	p.Lys1021AsnfsTer18(p.K1021Nfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000177648
Start	112435260:112435260(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3151delT
AA Mutation	p.Trp1051GlyfsTer36(p.W1051Gfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000177648
Start	112425706:112425706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.577C>T
AA Mutation	p.Gln193Ter(p.Q193*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000177648
Start	112430978:112430979(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1436dupA
AA Mutation	p.Asn479LysfsTer2(p.N479Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	23
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000177648
Start	112430446:112430446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript