Mutation

Primary Site >> Stomach Cancer

Gene >> SLCO5A1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69682230:69682230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1736A>C
AA Mutation	p.Asn579Thr(p.N579T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69831974:69831974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700G>A
AA Mutation	p.Asp234Asn(p.D234N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69705191:69705191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1462C>A
AA Mutation	p.Leu488Ile(p.L488I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260126
Start	69831767:69831767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907G>A
AA Mutation	p.Ala303Thr(p.A303T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69673212:69673212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2204G>C
AA Mutation	p.Arg735Pro(p.R735P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69673231:69673231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2185T>C
AA Mutation	p.Tyr729His(p.Y729H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69673054:69673054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548263300
CDS Mutation	c.2362G>A
AA Mutation	p.Asp788Asn(p.D788N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69673000:69673000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2416G>A
AA Mutation	p.Glu806Lys(p.E806K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69682210:69682210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1756G>A
AA Mutation	p.Val586Ile(p.V586I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69832300:69832300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374C>T
AA Mutation	p.Thr125Met(p.T125M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69679582:69679582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151145765
CDS Mutation	c.1820G>A
AA Mutation	p.Arg607His(p.R607H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69761851:69761851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.932T>G
AA Mutation	p.Leu311Arg(p.L311R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69831796:69831796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878T>C
AA Mutation	p.Val293Ala(p.V293A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69705062:69705062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1591C>G
AA Mutation	p.Leu531Val(p.L531V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69672879:69672879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2537C>T
AA Mutation	p.Pro846Leu(p.P846L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69705218:69705218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141622109
CDS Mutation	c.1435G>A
AA Mutation	p.Val479Ile(p.V479I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69831865:69831865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.809C>T
AA Mutation	p.Ala270Val(p.A270V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69682274:69682274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1692C>A
AA Mutation	p.His564Gln(p.H564Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69672921:69672921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2495C>A
AA Mutation	p.Ser832Tyr(p.S832Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69672892:69672892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2524G>A
AA Mutation	p.Ala842Thr(p.A842T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69673147:69673147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2269T>G
AA Mutation	p.Trp757Gly(p.W757G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69832529:69832529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.145A>G
AA Mutation	p.Ser49Gly(p.S49G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000260126
Start	69832220:69832220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761242652
CDS Mutation	c.454G>A
AA Mutation	p.Val152Ile(p.V152I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260126
Start	69832416:69832416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777138818
CDS Mutation	c.258G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260126
Start	69832038:69832038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260126
Start	69673214:69673214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2202T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260126
Start	69705168:69705168(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1485delA
AA Mutation	p.Lys495AsnfsTer2(p.K495Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260126
Start	69672980:69672980(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2436delA
AA Mutation	p.Ile814SerfsTer16(p.I814Sfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260126
Start	69832011:69832011(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.663delC
AA Mutation	p.Tyr222ThrfsTer6(p.Y222Tfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260126
Start	69832010:69832011(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.663dupC
AA Mutation	p.Tyr222LeufsTer38(p.Y222Lfs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript