Mutation

Primary Site >> Stomach Cancer

Gene >> SSH2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29631014:29631014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4099A>C
AA Mutation	p.Ser1367Arg(p.S1367R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29630993:29630993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761793558
CDS Mutation	c.4120G>A
AA Mutation	p.Val1374Met(p.V1374M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29677724:29677724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.416G>A
AA Mutation	p.Gly139Asp(p.G139D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29631212:29631212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533970239
CDS Mutation	c.3901G>A
AA Mutation	p.Ala1301Thr(p.A1301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29667213:29667213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759933801
CDS Mutation	c.739C>T
AA Mutation	p.Arg247Cys(p.R247C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29636273:29636273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1876T>C
AA Mutation	p.Ser626Pro(p.S626P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29631019:29631019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4094T>C
AA Mutation	p.Leu1365Ser(p.L1365S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29630911:29630911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4202A>G
AA Mutation	p.His1401Arg(p.H1401R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29632481:29632481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774614207
CDS Mutation	c.2632C>T
AA Mutation	p.Arg878Trp(p.R878W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29650738:29650738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061A>G
AA Mutation	p.Tyr354Cys(p.Y354C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29672047:29672047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616G>A
AA Mutation	p.Val206Met(p.V206M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29632427:29632427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763639780
CDS Mutation	c.2686C>T
AA Mutation	p.Arg896Cys(p.R896C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29630942:29630942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778253169
CDS Mutation	c.4171G>A
AA Mutation	p.Val1391Met(p.V1391M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29636176:29636176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1973A>C
AA Mutation	p.Lys658Thr(p.K658T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29636606:29636606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1543G>T
AA Mutation	p.Asp515Tyr(p.D515Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29631563:29631563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144293105
CDS Mutation	c.3550G>A
AA Mutation	p.Ala1184Thr(p.A1184T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29667168:29667168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784A>G
AA Mutation	p.Met262Val(p.M262V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29650795:29650795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747725784
CDS Mutation	c.1004G>A
AA Mutation	p.Arg335Gln(p.R335Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29636118:29636118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2031G>T
AA Mutation	p.Glu677Asp(p.E677D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29672092:29672092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571G>A
AA Mutation	p.Ala191Thr(p.A191T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000269033
Start	29632090:29632090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3023G>A
AA Mutation	p.Arg1008Lys(p.R1008K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269033
Start	29631564:29631564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755607432
CDS Mutation	c.3549C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269033
Start	29636577:29636577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1572A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269033
Start	29703032:29703032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746459403
CDS Mutation	c.138T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269033
Start	29631615:29631615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3498C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269033
Start	29630922:29630922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4191C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269033
Start	29630910:29630910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4203C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269033
Start	29632357:29632357(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs752567808
CDS Mutation	c.2756delC
AA Mutation	p.Pro919GlnfsTer12(p.P919Qfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000269033
Start	29676830:29676830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523C>T
AA Mutation	p.Gln175Ter(p.Q175*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269033
Start	29636690:29636691(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1458dupC
AA Mutation	p.Ser487LeufsTer7(p.S487Lfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269033
Start	29636522:29636523(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1626dupT
AA Mutation	p.Glu543Ter(p.E543*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript