Mutation

Primary Site >> Stomach Cancer

Gene >> MORC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109027857:109027857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1598C>A
AA Mutation	p.Pro533Gln(p.P533Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109005249:109005249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1834T>G
AA Mutation	p.Phe612Val(p.F612V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109032817:109032817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1468C>A
AA Mutation	p.Leu490Ile(p.L490I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109057440:109057440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747855351
CDS Mutation	c.1078G>A
AA Mutation	p.Val360Ile(p.V360I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	108963425:108963425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2788A>G
AA Mutation	p.Lys930Glu(p.K930E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109069746:109069746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.701G>T
AA Mutation	p.Arg234Met(p.R234M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109057381:109057381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1137G>A
AA Mutation	p.Met379Ile(p.M379I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	108959095:108959095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2825A>G
AA Mutation	p.Gln942Arg(p.Q942R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	108969715:108969715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2558A>G
AA Mutation	p.Gln853Arg(p.Q853R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232603
Start	109054870:109054870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767418985
CDS Mutation	c.1188C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232603
Start	108959052:108959052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2868T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	108986903:108986903(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2234delA
AA Mutation	p.Lys745ArgfsTer6(p.K745Rfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	108963572:108963572(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs757379917
CDS Mutation	c.2641delA
AA Mutation	p.Ile881Ter(p.I881*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	109103893:109103893(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.179delG
AA Mutation	p.Gly60AspfsTer13(p.G60Dfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	109032764:109032764(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1521delT
AA Mutation	p.Phe507LeufsTer20(p.F507Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	109099393:109099393(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.388delT
AA Mutation	p.Ser130LeufsTer14(p.S130Lfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	108963572:108963573(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2640_2641delAA
AA Mutation	p.Lys880AsnfsTer11(p.K880Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	109054766:109054766(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1292delG
AA Mutation	p.Gly431AspfsTer18(p.G431Dfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript