Mutation

Primary Site >> Stomach Cancer

Gene >> MAP3K5

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136601833:136601833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2826C>G
AA Mutation	p.Ser942Arg(p.S942R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136567799:136567799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745309811
CDS Mutation	c.3593A>G
AA Mutation	p.His1198Arg(p.H1198R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136605349:136605349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2539G>A
AA Mutation	p.Ala847Thr(p.A847T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136694149:136694149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1244G>A
AA Mutation	p.Gly415Glu(p.G415E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136592590:136592590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764549591
CDS Mutation	c.2903C>T
AA Mutation	p.Pro968Leu(p.P968L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136656392:136656392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1595C>T
AA Mutation	p.Pro532Leu(p.P532L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136583727:136583727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199742266
CDS Mutation	c.3239C>T
AA Mutation	p.Pro1080Leu(p.P1080L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136697244:136697244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950T>C
AA Mutation	p.Leu317Pro(p.L317P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359015
Start	136592478:136592478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150394997
CDS Mutation	c.3015C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359015
Start	136583726:136583726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3240G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359015
Start	136601893:136601893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2766T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359015
Start	136605224:136605224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2664A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359015
Start	136622853:136622854(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2143_2144dupGA
AA Mutation	p.Asp715GlufsTer13(p.D715Efs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript