Mutation

Primary Site >> Stomach Cancer

Gene >> NFATC2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51435276:51435276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1944G>T
AA Mutation	p.Lys648Asn(p.K648N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51474103:51474103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1585C>T
AA Mutation	p.Arg529Trp(p.R529W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51432663:51432663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751513686
CDS Mutation	c.2126C>T
AA Mutation	p.Pro709Leu(p.P709L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51523213:51523213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374413124
CDS Mutation	c.1028G>A
AA Mutation	p.Arg343His(p.R343H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51524012:51524012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.229A>G
AA Mutation	p.Ser77Gly(p.S77G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51516884:51516884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199662497
CDS Mutation	c.1232G>A
AA Mutation	p.Arg411Gln(p.R411Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51474141:51474141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775920655
CDS Mutation	c.1547C>T
AA Mutation	p.Ala516Val(p.A516V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51435284:51435284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773542213
CDS Mutation	c.1936C>T
AA Mutation	p.Arg646Trp(p.R646W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51523241:51523241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000G>A
AA Mutation	p.Ala334Thr(p.A334T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51523430:51523430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811C>T
AA Mutation	p.Arg271Cys(p.R271C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51432384:51432384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749298884
CDS Mutation	c.2405C>T
AA Mutation	p.Pro802Leu(p.P802L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51432571:51432571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758439316
CDS Mutation	c.2218G>A
AA Mutation	p.Ala740Thr(p.A740T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51516941:51516941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1175C>T
AA Mutation	p.Ala392Val(p.A392V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51523670:51523670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571G>A
AA Mutation	p.Val191Ile(p.V191I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51523289:51523289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952A>T
AA Mutation	p.Ile318Phe(p.I318F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51523975:51523975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556060763
CDS Mutation	c.266C>T
AA Mutation	p.Pro89Leu(p.P89L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51432322:51432322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528842461
CDS Mutation	c.2467G>A
AA Mutation	p.Gly823Arg(p.G823R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51523540:51523540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701G>A
AA Mutation	p.Arg234His(p.R234H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51516795:51516795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321C>T
AA Mutation	p.Pro441Ser(p.P441S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51523972:51523972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.269A>G
AA Mutation	p.Asp90Gly(p.D90G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51523306:51523306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376937921
CDS Mutation	c.935C>T
AA Mutation	p.Thr312Met(p.T312M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000396009
Start	51475597:51475597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1396C>T
AA Mutation	p.Arg466Trp(p.R466W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396009
Start	51523845:51523845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396009
Start	51523554:51523554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396009
Start	51432452:51432452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142272268
CDS Mutation	c.2337C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396009
Start	51435243:51435243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142900177
CDS Mutation	c.1977C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396009
Start	51523563:51523563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000396009
Start	51435300:51435300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1920T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396009
Start	51542488:51542488(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.12delC
AA Mutation	p.Glu5SerfsTer35(p.E5Sfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396009
Start	51432115:51432115(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2674delG
AA Mutation	p.Val892Ter(p.V892*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396009
Start	51454597:51454597(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1800delG
AA Mutation	p.Gln601ArgfsTer54(p.Q601Rfs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript