Mutation

Primary Site >> Stomach Cancer

Gene >> CCAR2

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22605820:22605820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47G>A
AA Mutation	p.Arg16His(p.R16H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22618837:22618837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2343C>A
AA Mutation	p.Asp781Glu(p.D781E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22617734:22617734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2029G>A
AA Mutation	p.Ala677Thr(p.A677T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22608034:22608034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.553G>A
AA Mutation	p.Gly185Ser(p.G185S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22615748:22615748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748696165
CDS Mutation	c.1444G>A
AA Mutation	p.Ala482Thr(p.A482T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22614186:22614186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799T>G
AA Mutation	p.Phe267Val(p.F267V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22615727:22615727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423G>A
AA Mutation	p.Ala475Thr(p.A475T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22607284:22607284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.446T>C
AA Mutation	p.Ile149Thr(p.I149T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22618713:22618713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2317G>A
AA Mutation	p.Glu773Lys(p.E773K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22618941:22618941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2447T>C
AA Mutation	p.Leu816Pro(p.L816P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22617699:22617699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201118681
CDS Mutation	c.1994G>A
AA Mutation	p.Gly665Glu(p.G665E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22617481:22617481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1907G>T
AA Mutation	p.Arg636Leu(p.R636L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000308511
Start	22615835:22615835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549430841
CDS Mutation	c.1531G>A
AA Mutation	p.Ala511Thr(p.A511T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308511
Start	22615470:22615470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1251G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308511
Start	22615747:22615747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151294361
CDS Mutation	c.1443C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308511
Start	22606125:22606125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308511
Start	22616110:22616110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1707C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308511
Start	22615462:22615462(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1249delC
AA Mutation	p.Arg417GlyfsTer89(p.R417Gfs*89)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308511
Start	22618844:22618844(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2354delC
AA Mutation	p.Pro785LeufsTer25(p.P785Lfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308511
Start	22615811:22615811(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1513delC
AA Mutation	p.Leu505Ter(p.L505*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000308511
Start	22619016:22619016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2521+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript