Mutation

Primary Site >> Stomach Cancer

Gene >> SPHKAP

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	227981847:227981847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4973T>C
AA Mutation	p.Val1658Ala(p.V1658A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228018690:228018690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2164A>G
AA Mutation	p.Lys722Glu(p.K722E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228019285:228019285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1569A>C
AA Mutation	p.Gln523His(p.Q523H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228021735:228021735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673A>G
AA Mutation	p.Ser225Gly(p.S225G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228017019:228017019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3835A>G
AA Mutation	p.Ser1279Gly(p.S1279G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228019233:228019233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621C>T
AA Mutation	p.Pro541Ser(p.P541S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228017136:228017136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3718C>T
AA Mutation	p.Pro1240Ser(p.P1240S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228017767:228017767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3087A>T
AA Mutation	p.Glu1029Asp(p.E1029D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228016884:228016884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3970A>G
AA Mutation	p.Ile1324Val(p.I1324V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228018006:228018006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2848G>C
AA Mutation	p.Asp950His(p.D950H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228021803:228021803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776316228
CDS Mutation	c.605A>G
AA Mutation	p.Asp202Gly(p.D202G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228019079:228019079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1775C>A
AA Mutation	p.Ala592Glu(p.A592E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000392056
Start	228027484:228027484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.306G>T
AA Mutation	p.Gln102His(p.Q102H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228181591:228181591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8G>A
AA Mutation	p.Gly3Asp(p.G3D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228017705:228017705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769323258
CDS Mutation	c.3149C>T
AA Mutation	p.Thr1050Met(p.T1050M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228016695:228016695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4159T>G
AA Mutation	p.Leu1387Val(p.L1387V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228017812:228017812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3042A>C
AA Mutation	p.Lys1014Asn(p.K1014N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228019344:228019344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1510G>A
AA Mutation	p.Ala504Thr(p.A504T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228016598:228016598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2396519
CDS Mutation	c.4256G>A
AA Mutation	p.Arg1419Gln(p.R1419Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228017420:228017420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3434A>G
AA Mutation	p.Glu1145Gly(p.E1145G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228019472:228019472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382C>T
AA Mutation	p.Ala461Val(p.A461V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	227995689:227995689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4454G>C
AA Mutation	p.Ser1485Thr(p.S1485T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228017625:228017625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755381681
CDS Mutation	c.3229C>T
AA Mutation	p.Arg1077Trp(p.R1077W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000392056
Start	228018065:228018065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2789C>T
AA Mutation	p.Ala930Val(p.A930V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392056
Start	228018256:228018256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2598C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392056
Start	228021943:228021943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392056
Start	228017635:228017635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772462016
CDS Mutation	c.3219C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392056
Start	228019069:228019069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1785T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392056
Start	228020020:228020020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392056
Start	228016561:228016561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4293T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392056
Start	228019498:228019498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1356T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392056
Start	228019111:228019111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1743C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392056
Start	228108870:228108870(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.208delA
AA Mutation	p.Ile70LeufsTer4(p.I70Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000392056
Start	228019128:228019128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1726A>T
AA Mutation	p.Arg576Ter(p.R576*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	35
Mutation Consequence	stop_gained
Transcription ID	ENST00000392056
Start	227981783:227981783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5037C>A
AA Mutation	p.Cys1679Ter(p.C1679*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392056
Start	228021854:228021855(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.550_553dupCTGG
AA Mutation	p.Val185AlafsTer19(p.V185Afs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript