Mutation

Primary Site >> Stomach Cancer

Gene >> CRMP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5825506:5825506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1615T>C
AA Mutation	p.Phe539Leu(p.F539L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5836027:5836027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1169A>C
AA Mutation	p.Lys390Thr(p.K390T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5836806:5836806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1069G>A
AA Mutation	p.Gly357Arg(p.G357R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5861155:5861155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.184G>T
AA Mutation	p.Gly62Trp(p.G62W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5841326:5841326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793G>A
AA Mutation	p.Ala265Thr(p.A265T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5861031:5861031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308T>C
AA Mutation	p.Met103Thr(p.M103T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5836850:5836850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371310830
CDS Mutation	c.1025C>T
AA Mutation	p.Ala342Val(p.A342V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5835989:5835989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752604466
CDS Mutation	c.1207G>A
AA Mutation	p.Val403Met(p.V403M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5825559:5825559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1562C>A
AA Mutation	p.Ser521Tyr(p.S521Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5825556:5825556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187171314
CDS Mutation	c.1565C>T
AA Mutation	p.Ser522Leu(p.S522L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5843122:5843122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.661G>A
AA Mutation	p.Glu221Lys(p.E221K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5836890:5836890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.985A>G
AA Mutation	p.Thr329Ala(p.T329A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000397890
Start	5841316:5841316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.803G>A
AA Mutation	p.Arg268Lys(p.R268K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5836891:5836891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5861198:5861198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5851453:5851453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.495A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5866694:5866694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149094396
CDS Mutation	c.102C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397890
Start	5836870:5836870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000397890
Start	5856152:5856152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469C>T
AA Mutation	p.Gln157Ter(p.Q157*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397890
Start	5821793:5821794(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1685dupC
AA Mutation	p.Gly563TrpfsTer19(p.G563Wfs*19)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript