Mutation

Primary Site >> Stomach Cancer

Gene >> UNC5C

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95206752:95206752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1778G>T
AA Mutation	p.Ser593Ile(p.S593I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95548838:95548838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.20C>T
AA Mutation	p.Ala7Val(p.A7V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95244999:95244999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.921A>G
AA Mutation	p.Ile307Met(p.I307M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95548799:95548799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.59T>C
AA Mutation	p.Leu20Pro(p.L20P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95219274:95219274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1340C>T
AA Mutation	p.Ala447Val(p.A447V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95219067:95219067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759735193
CDS Mutation	c.1547G>A
AA Mutation	p.Ser516Asn(p.S516N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95242471:95242471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371874775
CDS Mutation	c.1066G>A
AA Mutation	p.Val356Ile(p.V356I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95335532:95335532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224A>T
AA Mutation	p.Lys75Met(p.K75M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95202825:95202825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774148486
CDS Mutation	c.2042G>A
AA Mutation	p.Arg681His(p.R681H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95219020:95219020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148691835
CDS Mutation	c.1594G>A
AA Mutation	p.Ala532Thr(p.A532T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95219214:95219214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147587723
CDS Mutation	c.1400A>G
AA Mutation	p.Asn467Ser(p.N467S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95206714:95206714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777197285
CDS Mutation	c.1816G>A
AA Mutation	p.Val606Ile(p.V606I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95301629:95301629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781088734
CDS Mutation	c.467G>A
AA Mutation	p.Arg156Gln(p.R156Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95219001:95219001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1613C>T
AA Mutation	p.Ser538Leu(p.S538L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95250514:95250514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748A>G
AA Mutation	p.Ser250Gly(p.S250G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95219058:95219058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1556A>C
AA Mutation	p.Asn519Thr(p.N519T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95202949:95202949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1918G>T
AA Mutation	p.Gly640Trp(p.G640W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95216206:95216206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1651A>G
AA Mutation	p.Ser551Gly(p.S551G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95170239:95170239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2545C>T
AA Mutation	p.Arg849Trp(p.R849W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000453304
Start	95220110:95220110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765485658
CDS Mutation	c.1175C>T
AA Mutation	p.Ala392Val(p.A392V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95170294:95170294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762675647
CDS Mutation	c.2490G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95242481:95242481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540870072
CDS Mutation	c.1056C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95548741:95548741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749134400
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95202764:95202764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2103C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95242468:95242468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000453304
Start	95548785:95548785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000453304
Start	95219143:95219143(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1471delC
AA Mutation	p.Gln491LysfsTer15(p.Q491Kfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000453304
Start	95245088:95245088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832C>T
AA Mutation	p.Arg278Ter(p.R278*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript