Mutation

Primary Site >> Stomach Cancer

Gene >> ULK1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131917536:131917536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2308C>T
AA Mutation	p.Arg770Cys(p.R770C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131908737:131908737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751254383
CDS Mutation	c.410G>A
AA Mutation	p.Arg137His(p.R137H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131895811:131895811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.233T>A
AA Mutation	p.Leu78Gln(p.L78Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131915948:131915948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1667G>T
AA Mutation	p.Ser556Ile(p.S556I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131909947:131909947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754C>T
AA Mutation	p.Arg252Trp(p.R252W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131918589:131918589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2419C>T
AA Mutation	p.His807Tyr(p.H807Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131908936:131908936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.529A>G
AA Mutation	p.Met177Val(p.M177V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131909974:131909974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781C>T
AA Mutation	p.Arg261Cys(p.R261C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131915917:131915917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200272214
CDS Mutation	c.1636C>T
AA Mutation	p.Arg546Cys(p.R546C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131919566:131919566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2779T>C
AA Mutation	p.Cys927Arg(p.C927R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131915981:131915981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192583536
CDS Mutation	c.1700G>A
AA Mutation	p.Arg567His(p.R567H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131911951:131911951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138390533
CDS Mutation	c.958G>A
AA Mutation	p.Glu320Lys(p.E320K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131919217:131919217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2517G>C
AA Mutation	p.Glu839Asp(p.E839D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131919249:131919249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147409347
CDS Mutation	c.2549C>T
AA Mutation	p.Thr850Met(p.T850M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131910787:131910787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775402283
CDS Mutation	c.935T>C
AA Mutation	p.Leu312Pro(p.L312P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000321867
Start	131916462:131916462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1943G>T
AA Mutation	p.Arg648Leu(p.R648L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321867
Start	131909944:131909944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321867
Start	131914382:131914382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772840184
CDS Mutation	c.1278C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321867
Start	131918576:131918576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753118432
CDS Mutation	c.2406C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321867
Start	131909807:131909807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321867
Start	131919478:131919478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780528784
CDS Mutation	c.2691G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321867
Start	131915372:131915372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766016454
CDS Mutation	c.1560G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321867
Start	131919247:131919247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2547C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321867
Start	131917521:131917521(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2299delC
AA Mutation	p.Gln767ArgfsTer57(p.Q767Rfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321867
Start	131916482:131916482(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1967delC
AA Mutation	p.Pro656LeufsTer168(p.P656Lfs*168)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321867
Start	131919313:131919313(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2618delG
AA Mutation	p.Gly873AlafsTer18(p.G873Afs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321867
Start	131916481:131916482(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1967dupC
AA Mutation	p.Arg657SerfsTer44(p.R657Sfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript