Mutation

Primary Site >> Stomach Cancer

Gene >> KCND2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120275537:120275537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905A>C
AA Mutation	p.Lys302Thr(p.K302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120275588:120275588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956G>A
AA Mutation	p.Ser319Asn(p.S319N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120275072:120275072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.440G>A
AA Mutation	p.Arg147His(p.R147H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120274793:120274793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161C>T
AA Mutation	p.Thr54Met(p.T54M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120732953:120732953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166T>C
AA Mutation	p.Ile389Thr(p.I389T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120275330:120275330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.698A>G
AA Mutation	p.Asp233Gly(p.D233G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120275670:120275670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038G>T
AA Mutation	p.Glu346Asp(p.E346D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120274640:120274640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>T
AA Mutation	p.Ala3Val(p.A3V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120275383:120275383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751G>T
AA Mutation	p.Ala251Ser(p.A251S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120742571:120742571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745746548
CDS Mutation	c.1436A>G
AA Mutation	p.His479Arg(p.H479R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120274730:120274730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.98A>G
AA Mutation	p.Gln33Arg(p.Q33R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120745802:120745802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1490A>G
AA Mutation	p.Gln497Arg(p.Q497R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120274729:120274729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97C>G
AA Mutation	p.Gln33Glu(p.Q33E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120275728:120275728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1096G>A
AA Mutation	p.Val366Ile(p.V366I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120747700:120747700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1735A>G
AA Mutation	p.Lys579Glu(p.K579E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120275164:120275164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.532C>T
AA Mutation	p.Pro178Ser(p.P178S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000331113
Start	120747683:120747683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761446789
CDS Mutation	c.1718G>A
AA Mutation	p.Arg573Gln(p.R573Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120275021:120275021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.389G>A
AA Mutation	p.Gly130Asp(p.G130D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000331113
Start	120275407:120275407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747264690
CDS Mutation	c.775C>T
AA Mutation	p.Arg259Cys(p.R259C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331113
Start	120275385:120275385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.753G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331113
Start	120274647:120274647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331113
Start	120275430:120275430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.798C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331113
Start	120275421:120275421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.789T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331113
Start	120275427:120275427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776818004
CDS Mutation	c.795C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331113
Start	120275664:120275664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1032C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331113
Start	120275150:120275150(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.520delG
AA Mutation	p.Ala174ProfsTer65(p.A174Pfs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000331113
Start	120747709:120747709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1744G>T
AA Mutation	p.Glu582Ter(p.E582*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript