Mutation

Primary Site >> Stomach Cancer

Gene >> CSF1R

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000286301
Start	150061595:150061595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1754G>A
AA Mutation	p.Gly585Asp(p.G585D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150080788:150080788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.286G>A
AA Mutation	p.Ala96Thr(p.A96T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150073457:150073457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.926T>C
AA Mutation	p.Leu309Pro(p.L309P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150078156:150078156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149911279
CDS Mutation	c.685G>A
AA Mutation	p.Val229Ile(p.V229I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150070228:150070228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1273C>T
AA Mutation	p.Pro425Ser(p.P425S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000286301
Start	150080334:150080334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310C>A
AA Mutation	p.Pro104Thr(p.P104T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150078228:150078228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613T>G
AA Mutation	p.Leu205Val(p.L205V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150068302:150068302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1539C>A
AA Mutation	p.Phe513Leu(p.F513L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150054091:150054091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2897C>T
AA Mutation	p.Pro966Leu(p.P966L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150059703:150059703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201569135
CDS Mutation	c.2129G>A
AA Mutation	p.Arg710His(p.R710H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150068262:150068262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1579G>A
AA Mutation	p.Ala527Thr(p.A527T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150080277:150080277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761316359
CDS Mutation	c.367G>A
AA Mutation	p.Ala123Thr(p.A123T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286301
Start	150069913:150069913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1470C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286301
Start	150068320:150068320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1521G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286301
Start	150068248:150068248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1593G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286301
Start	150080266:150080266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286301
Start	150061775:150061775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567201624
CDS Mutation	c.1701G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286301
Start	150057515:150057515(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2210delT
AA Mutation	p.Phe737SerfsTer26(p.F737Sfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286301
Start	150078233:150078233(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.608delC
AA Mutation	p.Pro203GlnfsTer3(p.P203Qfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286301
Start	150080913:150080913(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.161delC
AA Mutation	p.Pro54HisfsTer58(p.P54Hfs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286301
Start	150080140:150080144(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.500_504delCCAAG
AA Mutation	p.Ala167ValfsTer62(p.A167Vfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286301
Start	150070248:150070248(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1253delT
AA Mutation	p.Leu418CysfsTer12(p.L418Cfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000286301
Start	150070208:150070208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1293G>A
AA Mutation	p.Trp431Ter(p.W431*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286301
Start	150069906:150069907(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1476dupG
AA Mutation	p.Ser493GlufsTer20(p.S493Efs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	25
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000286301
Start	150069871:150069871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1510+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript