Mutation

Primary Site >> Stomach Cancer

Gene >> ZFX

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304543
Start	24210382:24210382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1424T>C
AA Mutation	p.Leu475Pro(p.L475P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304543
Start	24208232:24208232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.955G>A
AA Mutation	p.Ala319Thr(p.A319T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304543
Start	24211294:24211294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2336A>G
AA Mutation	p.Glu779Gly(p.E779G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304543
Start	24179590:24179590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.466G>A
AA Mutation	p.Val156Met(p.V156M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304543
Start	24210428:24210428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372941972
CDS Mutation	c.1470C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304543
Start	24210284:24210284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1326G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304543
Start	24210701:24210701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143557208
CDS Mutation	c.1743C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304543
Start	24210473:24210473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1515T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304543
Start	24211017:24211017(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2065delA
AA Mutation	p.Met689CysfsTer17(p.M689Cfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript