Mutation

Primary Site >> Stomach Cancer

Gene >> HOXB3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311626
Start	48552456:48552456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19T>C
AA Mutation	p.Tyr7His(p.Y7H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311626
Start	48550815:48550815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200719688
CDS Mutation	c.815C>T
AA Mutation	p.Thr272Met(p.T272M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311626
Start	48550461:48550461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1169C>A
AA Mutation	p.Pro390His(p.P390H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311626
Start	48552444:48552444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745805494
CDS Mutation	c.31G>A
AA Mutation	p.Ala11Thr(p.A11T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311626
Start	48552122:48552122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353G>T
AA Mutation	p.Gly118Val(p.G118V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311626
Start	48550633:48550633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.997G>A
AA Mutation	p.Val333Ile(p.V333I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311626
Start	48552154:48552154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311626
Start	48550856:48550856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311626
Start	48552252:48552252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.223A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311626
Start	48550946:48550946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311626
Start	48551147:48551147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557227249
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311626
Start	48551165:48551165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311626
Start	48552340:48552340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.135C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311626
Start	48550563:48550563(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1067delG
AA Mutation	p.Gly356AlafsTer73(p.G356Afs*73)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311626
Start	48550857:48550857(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.773delG
AA Mutation	p.Gly258AlafsTer19(p.G258Afs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311626
Start	48552034:48552034(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.441delC
AA Mutation	p.Gly148AlafsTer72(p.G148Afs*72)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript