Mutation

Primary Site >> Stomach Cancer

Gene >> ALX4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44275512:44275512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613G>A
AA Mutation	p.Ala205Thr(p.A205T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44275509:44275509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140457891
CDS Mutation	c.616G>A
AA Mutation	p.Asp206Asn(p.D206N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44275444:44275444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681G>T
AA Mutation	p.Glu227Asp(p.E227D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329255
Start	44265173:44265173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149897209
CDS Mutation	c.917C>T
AA Mutation	p.Pro306Leu(p.P306L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329255
Start	44265031:44265031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1059T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329255
Start	44264908:44264908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149365713
CDS Mutation	c.1182G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329255
Start	44309934:44309934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329255
Start	44275449:44275449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749075893
CDS Mutation	c.676C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329255
Start	44265074:44265074(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1016delC
AA Mutation	p.Pro339LeufsTer12(p.P339Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	start_lost
Transcription ID	ENST00000329255
Start	44310061:44310061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript