Mutation

Primary Site >> Stomach Cancer

Gene >> ZNF217

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53582697:53582697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141827117
CDS Mutation	c.130G>A
AA Mutation	p.Ala44Thr(p.A44T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53582693:53582693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134T>C
AA Mutation	p.Val45Ala(p.V45A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53581754:53581754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1073C>G
AA Mutation	p.Ala358Gly(p.A358G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53576753:53576753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758311512
CDS Mutation	c.2011G>A
AA Mutation	p.Ala671Thr(p.A671T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53581551:53581551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276G>A
AA Mutation	p.Ala426Thr(p.A426T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53571838:53571838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3053C>T
AA Mutation	p.Ser1018Leu(p.S1018L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53576723:53576723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2041G>A
AA Mutation	p.Asp681Asn(p.D681N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53582192:53582192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759065216
CDS Mutation	c.635C>T
AA Mutation	p.Ser212Phe(p.S212F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302342
Start	53575828:53575828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2936A>T
AA Mutation	p.Asp979Val(p.D979V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53577222:53577222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1542G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53581951:53581951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770189300
CDS Mutation	c.876G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53582632:53582632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53576811:53576811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202034493
CDS Mutation	c.1953G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53581879:53581879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748689017
CDS Mutation	c.948G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53577024:53577024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1740T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53582608:53582608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53582506:53582506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767630244
CDS Mutation	c.321G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53576217:53576217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2547T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302342
Start	53576735:53576735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2029A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302342
Start	53576687:53576687(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2077delG
AA Mutation	p.Ala693LeufsTer10(p.A693Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000302342
Start	53577189:53577189(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1575delA
AA Mutation	p.Lys525AsnfsTer23(p.K525Nfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript