Mutation

Primary Site >> Stomach Cancer

Gene >> CNTN1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40993197:40993197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760051219
CDS Mutation	c.2041G>A
AA Mutation	p.Val681Met(p.V681M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	41029160:41029160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2921T>C
AA Mutation	p.Val974Ala(p.V974A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	41014252:41014252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2138T>G
AA Mutation	p.Val713Gly(p.V713G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40933524:40933524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767G>A
AA Mutation	p.Gly256Asp(p.G256D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40980974:40980974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1870T>C
AA Mutation	p.Trp624Arg(p.W624R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40933720:40933720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201607834
CDS Mutation	c.827G>A
AA Mutation	p.Arg276Gln(p.R276Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	41016691:41016691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2194A>G
AA Mutation	p.Arg732Gly(p.R732G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40933499:40933499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742T>C
AA Mutation	p.Phe248Leu(p.F248L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40937679:40937679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1220A>C
AA Mutation	p.Lys407Thr(p.K407T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	41016811:41016811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753554748
CDS Mutation	c.2314G>A
AA Mutation	p.Glu772Lys(p.E772K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40922275:40922275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247G>A
AA Mutation	p.Asp83Asn(p.D83N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	41025175:41025175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2549A>G
AA Mutation	p.Lys850Arg(p.K850R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40929894:40929894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595G>A
AA Mutation	p.Ala199Thr(p.A199T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	41014293:41014293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2179T>C
AA Mutation	p.Trp727Arg(p.W727R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	41029210:41029210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2971A>G
AA Mutation	p.Lys991Glu(p.K991E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40933834:40933834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941A>G
AA Mutation	p.Asn314Ser(p.N314S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40980935:40980935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1831A>G
AA Mutation	p.Arg611Gly(p.R611G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	41025238:41025238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2612T>G
AA Mutation	p.Leu871Arg(p.L871R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40933753:40933753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860A>C
AA Mutation	p.Glu287Ala(p.E287A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40929859:40929859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs4408370
CDS Mutation	c.560G>A
AA Mutation	p.Arg187Gln(p.R187Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40944066:40944066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1579G>A
AA Mutation	p.Ala527Thr(p.A527T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	40918750:40918750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206C>T
AA Mutation	p.Ala69Val(p.A69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000347616
Start	41025217:41025217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2591A>G
AA Mutation	p.Tyr864Cys(p.Y864C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000347616
Start	41014297:41014297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201782849
CDS Mutation	c.2183C>T
AA Mutation	p.Ala728Val(p.A728V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347616
Start	41029072:41029072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2833A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347616
Start	40939414:40939414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347616
Start	40939474:40939474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1368C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347616
Start	40980958:40980958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1854T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347616
Start	41069999:41069999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3021G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347616
Start	41027888:41027888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2742A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347616
Start	40981018:40981018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1914T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347616
Start	41020382:41020383(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2465_2466insCCATTTGTCAA
AA Mutation	p.Ser823HisfsTer15(p.S823Hfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript