Mutation

Primary Site >> Stomach Cancer

Gene >> CNTN3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74301743:74301743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1849T>C
AA Mutation	p.Ser617Pro(p.S617P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74301527:74301527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1966A>G
AA Mutation	p.Lys656Glu(p.K656E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74285386:74285386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2623T>C
AA Mutation	p.Tyr875His(p.Y875H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74298092:74298092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2266C>A
AA Mutation	p.Pro756Thr(p.P756T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74362022:74362022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1232C>T
AA Mutation	p.Ser411Leu(p.S411L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74302705:74302705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1771G>C
AA Mutation	p.Asp591His(p.D591H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74362004:74362004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1250A>C
AA Mutation	p.Lys417Thr(p.K417T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74362018:74362018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778473765
CDS Mutation	c.1236G>T
AA Mutation	p.Lys412Asn(p.K412N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74371244:74371244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610A>C
AA Mutation	p.Asn204His(p.N204H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74424895:74424895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775718393
CDS Mutation	c.404G>A
AA Mutation	p.Arg135His(p.R135H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74295207:74295207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2431G>T
AA Mutation	p.Ala811Ser(p.A811S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74334788:74334788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1615G>T
AA Mutation	p.Gly539Trp(p.G539W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74424896:74424896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569008734
CDS Mutation	c.403C>T
AA Mutation	p.Arg135Cys(p.R135C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74295197:74295197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2441T>C
AA Mutation	p.Leu814Pro(p.L814P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74424860:74424860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.439C>T
AA Mutation	p.Pro147Ser(p.P147S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74298139:74298139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2219T>A
AA Mutation	p.Phe740Tyr(p.F740Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74302720:74302720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1756G>T
AA Mutation	p.Val586Phe(p.V586F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74371363:74371363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752936529
CDS Mutation	c.491C>T
AA Mutation	p.Ser164Leu(p.S164L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74267274:74267274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2809G>A
AA Mutation	p.Gly937Arg(p.G937R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74369305:74369305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830A>C
AA Mutation	p.Lys277Thr(p.K277T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74371216:74371216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638C>A
AA Mutation	p.Pro213His(p.P213H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000263665
Start	74299894:74299894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752462306
CDS Mutation	c.2140C>T
AA Mutation	p.Arg714Trp(p.R714W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74301747:74301747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1845A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74336595:74336595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1428T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74361931:74361931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1323T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74369924:74369924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.726T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74266620:74266620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2847C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74301522:74301522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111626135
CDS Mutation	c.1971G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74369256:74369256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.879T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74336595:74336595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1428T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74334795:74334795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1608T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74285405:74285405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2604C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74371233:74371233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.621G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74299931:74299931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2103A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263665
Start	74285351:74285351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142860919
CDS Mutation	c.2658C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263665
Start	74369218:74369218(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.917delA
AA Mutation	p.Asn306MetfsTer19(p.N306Mfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	37
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263665
Start	74499705:74499705(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.136delA
AA Mutation	p.Ile46Ter(p.I46*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000263665
Start	74365638:74365638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1011G>A
AA Mutation	p.Trp337Ter(p.W337*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000263665
Start	74369228:74369228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907C>T
AA Mutation	p.Arg303Ter(p.R303*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263665
Start	74285471:74285472(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2537dupG
AA Mutation	p.Gly847TrpfsTer8(p.G847Wfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	41
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000263665
Start	74266602:74266603(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2864_2865insTGATGTCAATAAAGT
AA Mutation	p.Thr955_Asn956insAspValAsnLysVal(p.T955_N956insDVNKV)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript