Mutation

Primary Site >> Stomach Cancer

Gene >> STK36

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218697557:218697557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2856G>A
AA Mutation	p.Met952Ile(p.M952I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218694528:218694528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2404G>A
AA Mutation	p.Ala802Thr(p.A802T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218697162:218697162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2710C>A
AA Mutation	p.Leu904Ile(p.L904I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218675398:218675398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770755293
CDS Mutation	c.359G>A
AA Mutation	p.Arg120His(p.R120H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218693962:218693962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199736780
CDS Mutation	c.2315G>A
AA Mutation	p.Arg772Gln(p.R772Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218692219:218692219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750796659
CDS Mutation	c.1841C>T
AA Mutation	p.Thr614Met(p.T614M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218694316:218694316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148974664
CDS Mutation	c.2389G>A
AA Mutation	p.Val797Ile(p.V797I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218699325:218699325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3781C>G
AA Mutation	p.Gln1261Glu(p.Q1261E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218698818:218698818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3274C>A
AA Mutation	p.Leu1092Met(p.L1092M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000295709
Start	218689922:218689922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763457446
CDS Mutation	c.1624A>G
AA Mutation	p.Thr542Ala(p.T542A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295709
Start	218689864:218689864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1566T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000295709
Start	218698848:218698848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3304G>T
AA Mutation	p.Glu1102Ter(p.E1102*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000295709
Start	218696526:218696526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2512-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript