Mutation

Primary Site >> Stomach Cancer

Gene >> SORCS3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105247320:105247320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3094G>C
AA Mutation	p.Ala1032Pro(p.A1032P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105043082:105043082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.982C>T
AA Mutation	p.Arg328Trp(p.R328W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105139424:105139424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1240T>G
AA Mutation	p.Tyr414Asp(p.Y414D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105255738:105255738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3274T>G
AA Mutation	p.Leu1092Val(p.L1092V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105147780:105147780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1466T>G
AA Mutation	p.Ile489Ser(p.I489S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105178133:105178133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375044945
CDS Mutation	c.1969G>A
AA Mutation	p.Gly657Arg(p.G657R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000369699
Start	105214612:105214612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2546A>C
AA Mutation	p.Glu849Ala(p.E849A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105245632:105245632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2959C>A
AA Mutation	p.Leu987Ile(p.L987I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105200094:105200094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2105A>G
AA Mutation	p.Gln702Arg(p.Q702R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	104977396:104977396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139171852
CDS Mutation	c.857C>T
AA Mutation	p.Ala286Val(p.A286V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105256833:105256833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3352T>C
AA Mutation	p.Ser1118Pro(p.S1118P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105252820:105252820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3151G>T
AA Mutation	p.Gly1051Cys(p.G1051C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	104842820:104842820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656A>G
AA Mutation	p.Asp219Gly(p.D219G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105139421:105139421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1237T>C
AA Mutation	p.Tyr413His(p.Y413H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	104641936:104641936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769279931
CDS Mutation	c.609G>C
AA Mutation	p.Trp203Cys(p.W203C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105139451:105139451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1267G>T
AA Mutation	p.Ala423Ser(p.A423S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105211238:105211238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2363T>G
AA Mutation	p.Leu788Arg(p.L788R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105262389:105262389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3502A>T
AA Mutation	p.Ile1168Phe(p.I1168F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105167309:105167309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751783356
CDS Mutation	c.1861G>A
AA Mutation	p.Val621Met(p.V621M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105247302:105247302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3076G>T
AA Mutation	p.Gly1026Cys(p.G1026C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105147713:105147713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753972777
CDS Mutation	c.1399C>T
AA Mutation	p.Arg467Cys(p.R467C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105214515:105214515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2449C>A
AA Mutation	p.Pro817Thr(p.P817T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105201130:105201130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2138G>T
AA Mutation	p.Cys713Phe(p.C713F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105147720:105147720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1406T>G
AA Mutation	p.Ile469Ser(p.I469S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105158980:105158980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1718T>C
AA Mutation	p.Leu573Pro(p.L573P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	104641938:104641938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611C>T
AA Mutation	p.Ser204Leu(p.S204L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000369699
Start	105201133:105201133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2141T>C
AA Mutation	p.Val714Ala(p.V714A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369699
Start	105200026:105200026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773731511
CDS Mutation	c.2037C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369699
Start	104977397:104977397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767410277
CDS Mutation	c.858G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369699
Start	105263335:105263335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375742143
CDS Mutation	c.3630C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369699
Start	105105479:105105479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1176T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369699
Start	105223174:105223174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2793C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369699
Start	105217019:105217019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143982937
CDS Mutation	c.2631C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369699
Start	105105455:105105455(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1155delT
AA Mutation	p.Phe385LeufsTer21(p.F385Lfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000369699
Start	105089836:105089836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1090G>T
AA Mutation	p.Gly364Ter(p.G364*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	stop_gained
Transcription ID	ENST00000369699
Start	105139442:105139442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1258G>T
AA Mutation	p.Glu420Ter(p.E420*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript