Mutation

Primary Site >> Stomach Cancer

Gene >> DZIP1L

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138103887:138103887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Cys(p.R29C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138103857:138103857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115A>C
AA Mutation	p.Ser39Arg(p.S39R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138103602:138103602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145919527
CDS Mutation	c.370C>T
AA Mutation	p.Arg124Cys(p.R124C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138094926:138094926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.644A>C
AA Mutation	p.Lys215Thr(p.K215T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138062908:138062908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2212G>C
AA Mutation	p.Glu738Gln(p.E738Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138071663:138071663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1595A>G
AA Mutation	p.Gln532Arg(p.Q532R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138103898:138103898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.74A>C
AA Mutation	p.Lys25Thr(p.K25T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138067569:138067569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1964C>T
AA Mutation	p.Thr655Ile(p.T655I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138103539:138103539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763322076
CDS Mutation	c.433C>T
AA Mutation	p.Arg145Trp(p.R145W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138084249:138084249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067A>T
AA Mutation	p.Gln356Leu(p.Q356L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138084162:138084162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769472234
CDS Mutation	c.1154G>A
AA Mutation	p.Arg385His(p.R385H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000327532
Start	138103515:138103515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457C>A
AA Mutation	p.Leu153Met(p.L153M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327532
Start	138068297:138068297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1686G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327532
Start	138092410:138092410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747418381
CDS Mutation	c.843C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327532
Start	138067691:138067691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147742959
CDS Mutation	c.1842G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327532
Start	138103750:138103750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327532
Start	138092437:138092437(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.816delA
AA Mutation	p.Lys272AsnfsTer17(p.K272Nfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327532
Start	138068162:138068162(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1821delG
AA Mutation	p.Met610Ter(p.M610*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327532
Start	138064679:138064679(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2091delT
AA Mutation	p.Phe697LeufsTer80(p.F697Lfs*80)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000327532
Start	138067692:138067692(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1841delC
AA Mutation	p.Pro614ArgfsTer69(p.P614Rfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript