Mutation

Primary Site >> Stomach Cancer

Gene >> PTK2B

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27420673:27420673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.400C>T
AA Mutation	p.Arg134Cys(p.R134C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27430945:27430945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761635419
CDS Mutation	c.739G>A
AA Mutation	p.Val247Ile(p.V247I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000346049
Start	27445917:27445917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753724315
CDS Mutation	c.2338C>T
AA Mutation	p.Arg780Trp(p.R780W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27454235:27454235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2677G>A
AA Mutation	p.Glu893Lys(p.E893K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000346049
Start	27445794:27445794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760981859
CDS Mutation	c.2215G>A
AA Mutation	p.Val739Ile(p.V739I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27436283:27436283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1276G>A
AA Mutation	p.Val426Ile(p.V426I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27458352:27458352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2873G>A
AA Mutation	p.Arg958Gln(p.R958Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27420682:27420682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.409C>A
AA Mutation	p.Pro137Thr(p.P137T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27440413:27440413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369239201
CDS Mutation	c.2011C>T
AA Mutation	p.Arg671Cys(p.R671C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27450821:27450821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771523736
CDS Mutation	c.2413C>T
AA Mutation	p.Arg805Trp(p.R805W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27397597:27397597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13T>A
AA Mutation	p.Ser5Thr(p.S5T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27439394:27439394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1830G>A
AA Mutation	p.Met610Ile(p.M610I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000346049
Start	27439398:27439398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759650182
CDS Mutation	c.1834G>A
AA Mutation	p.Ala612Thr(p.A612T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27440396:27440396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755668710
CDS Mutation	c.1994A>G
AA Mutation	p.Asp665Gly(p.D665G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27422325:27422325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Cys(p.R165C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27440393:27440393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1991A>G
AA Mutation	p.Tyr664Cys(p.Y664C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000346049
Start	27397764:27397764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180A>C
AA Mutation	p.Lys60Asn(p.K60N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346049
Start	27444235:27444235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144972819
CDS Mutation	c.2178G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346049
Start	27440421:27440421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149334019
CDS Mutation	c.2019C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346049
Start	27442974:27442974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2139C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346049
Start	27419921:27419921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144837322
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346049
Start	27454593:27454593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754219845
CDS Mutation	c.2796G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346049
Start	27432354:27432354(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.985delC
AA Mutation	p.Gln329ArgfsTer10(p.Q329Rfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346049
Start	27433500:27433506(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1057_1063delCGGCTGC
AA Mutation	p.Leu354ValfsTer27(p.L354Vfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346049
Start	27454262:27454262(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2709delC
AA Mutation	p.Glu904ArgfsTer7(p.E904Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript