Mutation

Primary Site >> Stomach Cancer

Gene >> DACT1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58646120:58646120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1497G>C
AA Mutation	p.Glu499Asp(p.E499D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645864:58645864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1241C>A
AA Mutation	p.Ser414Tyr(p.S414Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58646763:58646763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2140G>A
AA Mutation	p.Ala714Thr(p.A714T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58646622:58646622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1999G>A
AA Mutation	p.Ala667Thr(p.A667T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58646128:58646128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1505T>C
AA Mutation	p.Val502Ala(p.V502A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58647007:58647007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773828792
CDS Mutation	c.2384C>T
AA Mutation	p.Thr795Met(p.T795M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645950:58645950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200763989
CDS Mutation	c.1327G>A
AA Mutation	p.Ala443Thr(p.A443T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58646652:58646652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2029C>T
AA Mutation	p.Arg677Trp(p.R677W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000335867
Start	58645781:58645781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1158G>T
AA Mutation	p.Gln386His(p.Q386H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58646786:58646786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2163T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58646762:58646762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778935261
CDS Mutation	c.2139C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58646744:58646744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2121G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58645262:58645262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.639C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58646987:58646987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780919243
CDS Mutation	c.2364C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58645949:58645949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1326C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335867
Start	58646279:58646279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571594579
CDS Mutation	c.1656G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335867
Start	58645665:58645665(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1048delA
AA Mutation	p.Thr350HisfsTer4(p.T350Hfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000335867
Start	58641621:58641621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508G>T
AA Mutation	p.Gly170Ter(p.G170*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000335867
Start	58646859:58646859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2236C>T
AA Mutation	p.Gln746Ter(p.Q746*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335867
Start	58645403:58645404(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.785dupA
AA Mutation	p.Asn262LysfsTer4(p.N262Kfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript