Mutation

Primary Site >> Stomach Cancer

Gene >> MSR1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16164178:16164178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704A>G
AA Mutation	p.His235Arg(p.H235R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16120501:16120501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1139A>G
AA Mutation	p.Glu380Gly(p.E380G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16164205:16164205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.677T>C
AA Mutation	p.Ile226Thr(p.I226T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16164104:16164104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.778G>A
AA Mutation	p.Glu260Lys(p.E260K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16110149:16110149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1292T>G
AA Mutation	p.Ile431Ser(p.I431S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16164110:16164110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772G>T
AA Mutation	p.Asp258Tyr(p.D258Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16177896:16177896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.93G>T
AA Mutation	p.Leu31Phe(p.L31F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16168489:16168489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599A>C
AA Mutation	p.Lys200Thr(p.K200T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16120529:16120529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746464687
CDS Mutation	c.1111T>A
AA Mutation	p.Trp371Arg(p.W371R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262101
Start	16177888:16177888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746296271
CDS Mutation	c.101C>T
AA Mutation	p.Pro34Leu(p.P34L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16150264:16150264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946A>C
AA Mutation	p.Ser316Arg(p.S316R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262101
Start	16143558:16143558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536722892
CDS Mutation	c.1033A>C
AA Mutation	p.Thr345Pro(p.T345P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16120593:16120593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1047A>C
AA Mutation	p.Lys349Asn(p.K349N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262101
Start	16168598:16168598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490T>C
AA Mutation	p.Ser164Pro(p.S164P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262101
Start	16150253:16150253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262101
Start	16110127:16110127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1314C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262101
Start	16110166:16110166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762285160
CDS Mutation	c.1275T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262101
Start	16155119:16155119(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.843delA
AA Mutation	p.Gly282GlufsTer18(p.G282Efs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000262101
Start	16110159:16110159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1282G>T
AA Mutation	p.Glu428Ter(p.E428*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262101
Start	16155118:16155119(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.843dupA
AA Mutation	p.Gly282ArgfsTer24(p.G282Rfs*24)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	21
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000262101
Start	16155145:16155145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.818-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript