Mutation

Primary Site >> Stomach Cancer

Gene >> AXL

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41220651:41220651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.101A>G
AA Mutation	p.Glu34Gly(p.E34G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41252909:41252909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1868T>C
AA Mutation	p.Met623Thr(p.M623T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41243626:41243626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1456G>C
AA Mutation	p.Glu486Gln(p.E486Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41220740:41220740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190C>T
AA Mutation	p.Pro64Ser(p.P64S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41238503:41238503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374067962
CDS Mutation	c.1028C>T
AA Mutation	p.Thr343Met(p.T343M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41259626:41259626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2407T>G
AA Mutation	p.Leu803Val(p.L803V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41253632:41253632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767628105
CDS Mutation	c.1960G>A
AA Mutation	p.Ala654Thr(p.A654T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41238098:41238098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200936572
CDS Mutation	c.938G>A
AA Mutation	p.Ser313Asn(p.S313N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41222009:41222009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539T>C
AA Mutation	p.Leu180Pro(p.L180P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41221955:41221955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.485C>A
AA Mutation	p.Ala162Asp(p.A162D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41239193:41239193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1164G>T
AA Mutation	p.Glu388Asp(p.E388D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41256517:41256517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2102A>G
AA Mutation	p.Asp701Gly(p.D701G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41253693:41253693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2021C>T
AA Mutation	p.Ala674Val(p.A674V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41257553:41257553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372169583
CDS Mutation	c.2257G>A
AA Mutation	p.Val753Met(p.V753M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41256489:41256489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2074G>A
AA Mutation	p.Gly692Arg(p.G692R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000301178
Start	41220710:41220710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160C>A
AA Mutation	p.Leu54Ile(p.L54I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301178
Start	41243679:41243679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1509C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301178
Start	41252952:41252952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771768158
CDS Mutation	c.1911C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301178
Start	41220700:41220700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.150C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301178
Start	41238477:41238477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1002G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301178
Start	41237991:41237991(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.836delC
AA Mutation	p.Pro279GlnfsTer18(p.P279Qfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301178
Start	41238480:41238480(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1010delC
AA Mutation	p.Pro337LeufsTer29(p.P337Lfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301178
Start	41238028:41238028(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.874delC
AA Mutation	p.His292IlefsTer5(p.H292Ifs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301178
Start	41259741:41259742(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2528dupC
AA Mutation	p.Thr844AsnfsTer6(p.T844Nfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	25
Mutation Consequence	splice_acceptor_variant;coding_sequence_variant;intron_variant
Transcription ID	ENST00000301178
Start	41239159:41239181(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1135-4_1153delCTAGGTGCTAATGGACATAGGGC
Mutation Classification	Splice_Site
Feature Type	Transcript