Mutation

Primary Site >> Stomach Cancer

Gene >> HLA-B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31356286:31356286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151341275
CDS Mutation	c.500C>T
AA Mutation	p.Thr167Ile(p.T167I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31355406:31355406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs185573735
CDS Mutation	c.806C>A
AA Mutation	p.Ala269Glu(p.A269E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000412585
Start	31354635:31354635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756666358
CDS Mutation	c.1043C>T
AA Mutation	p.Ala348Val(p.A348V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31355415:31355415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797A>G
AA Mutation	p.Gln266Arg(p.Q266R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31355503:31355503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709A>T
AA Mutation	p.Ile237Phe(p.I237F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31355502:31355502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710T>G
AA Mutation	p.Ile237Ser(p.I237S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31356882:31356882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs281864589
CDS Mutation	c.149G>A
AA Mutation	p.Gly50Asp(p.G50D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31356415:31356415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371G>A
AA Mutation	p.Gly124Asp(p.G124D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31355439:31355439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773G>A
AA Mutation	p.Arg258Lys(p.R258K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31355516:31355516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.696C>A
AA Mutation	p.Phe232Leu(p.F232L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000412585
Start	31355517:31355517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.695T>A
AA Mutation	p.Phe232Tyr(p.F232Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31355586:31355586(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.626delC
AA Mutation	p.Pro209GlnfsTer5(p.P209Qfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31355576:31355579(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.633_636delACAC
AA Mutation	p.His212Ter(p.H212*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31356791:31356791(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.240delG
AA Mutation	p.Pro81ArgfsTer70(p.P81Rfs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31357140:31357140(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.19delC
AA Mutation	p.Arg7GlufsTer13(p.R7Efs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31355492:31355493(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.719_720delCC
AA Mutation	p.Thr240MetfsTer13(p.T240Mfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31355585:31355586(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs748204482
CDS Mutation	c.626dupC
AA Mutation	p.Thr211AspfsTer10(p.T211Dfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412585
Start	31356401:31356402(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.384dupG
AA Mutation	p.Pro129AlafsTer10(p.P129Afs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	19
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000412585
Start	31355106:31355106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	20
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000412585
Start	31355335:31355352(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.860_877delATGAGGGGCTGCCGAAGC
AA Mutation	p.His287_Lys292del(p.H287_K292del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript