Mutation

Primary Site >> Stomach Cancer

Gene >> KCND3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111981769:111981769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.958G>A
AA Mutation	p.Glu320Lys(p.E320K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111776180:111776180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199663609
CDS Mutation	c.1865C>T
AA Mutation	p.Ala622Val(p.A622V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111981975:111981975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.752G>A
AA Mutation	p.Arg251His(p.R251H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111778467:111778467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1487C>A
AA Mutation	p.Pro496His(p.P496H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111981717:111981717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010C>T
AA Mutation	p.Thr337Ile(p.T337I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982521:111982521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781094017
CDS Mutation	c.206C>T
AA Mutation	p.Thr69Met(p.T69M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111981775:111981775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.952G>A
AA Mutation	p.Ala318Thr(p.A318T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111981969:111981969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758G>A
AA Mutation	p.Arg253His(p.R253H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982617:111982617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110G>A
AA Mutation	p.Arg37Gln(p.R37Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111981700:111981700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027G>A
AA Mutation	p.Glu343Lys(p.E343K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982220:111982220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507G>A
AA Mutation	p.Met169Ile(p.M169I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982432:111982432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.295C>T
AA Mutation	p.Arg99Cys(p.R99C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982618:111982618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.109C>T
AA Mutation	p.Arg37Trp(p.R37W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111787054:111787054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1159T>C
AA Mutation	p.Cys387Arg(p.C387R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111981822:111981822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905G>A
AA Mutation	p.Arg302His(p.R302H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982471:111982471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256C>T
AA Mutation	p.Arg86Trp(p.R86W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982447:111982447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>A
AA Mutation	p.Val94Met(p.V94M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000315987
Start	111982066:111982066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661C>T
AA Mutation	p.Arg221Cys(p.R221C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315987
Start	111780702:111780702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762936059
CDS Mutation	c.1359G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315987
Start	111981629:111981629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1098C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315987
Start	111982343:111982343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000315987
Start	111776134:111776134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1911C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000315987
Start	111786945:111786945(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1268delA
AA Mutation	p.Lys423ArgfsTer34(p.K423Rfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000315987
Start	111982544:111982544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.183C>G
AA Mutation	p.Tyr61Ter(p.Y61*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript