Mutation

Primary Site >> Stomach Cancer

Gene >> NUAK1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106086802:106086802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779923959
CDS Mutation	c.445C>T
AA Mutation	p.Arg149Cys(p.R149C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067949:106067949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839G>A
AA Mutation	p.Arg280Gln(p.R280Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067325:106067325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200489873
CDS Mutation	c.1463C>T
AA Mutation	p.Ser488Leu(p.S488L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067436:106067436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747705556
CDS Mutation	c.1352C>T
AA Mutation	p.Pro451Leu(p.P451L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067617:106067617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1171A>C
AA Mutation	p.Lys391Gln(p.K391Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106066992:106066992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762178790
CDS Mutation	c.1796G>A
AA Mutation	p.Arg599His(p.R599H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067650:106067650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138T>G
AA Mutation	p.Ser380Ala(p.S380A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067068:106067068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186215853
CDS Mutation	c.1720G>A
AA Mutation	p.Asp574Asn(p.D574N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067059:106067059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768722408
CDS Mutation	c.1729G>A
AA Mutation	p.Val577Met(p.V577M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067153:106067153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1635G>A
AA Mutation	p.Met545Ile(p.M545I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067559:106067559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771843801
CDS Mutation	c.1229G>A
AA Mutation	p.Arg410His(p.R410H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106138553:106138553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751592845
CDS Mutation	c.101T>G
AA Mutation	p.Leu34Arg(p.L34R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106086816:106086816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431T>C
AA Mutation	p.Ile144Thr(p.I144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067014:106067014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777676118
CDS Mutation	c.1774C>T
AA Mutation	p.Arg592Cys(p.R592C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106072791:106072791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632C>T
AA Mutation	p.Thr211Met(p.T211M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106070809:106070809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797G>A
AA Mutation	p.Ser266Asn(p.S266N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067638:106067638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1150G>T
AA Mutation	p.Ala384Ser(p.A384S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261402
Start	106086761:106086761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267603280
CDS Mutation	c.486C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261402
Start	106138566:106138566(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.88delG
AA Mutation	p.Ala30ArgfsTer13(p.A30Rfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261402
Start	106072786:106072786(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.637delT
AA Mutation	p.Cys213ValfsTer75(p.C213Vfs*75)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000261402
Start	106138479:106138479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175G>T
AA Mutation	p.Glu59Ter(p.E59*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000261402
Start	106067323:106067323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465G>T
AA Mutation	p.Glu489Ter(p.E489*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000261402
Start	106070772:106070772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript