Mutation

Primary Site >> Stomach Cancer

Gene >> CNTNAP1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42692664:42692664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144243880
CDS Mutation	c.2696G>A
AA Mutation	p.Arg899Gln(p.R899Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42687024:42687024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1022G>A
AA Mutation	p.Arg341His(p.R341H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42693318:42693318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779511124
CDS Mutation	c.2774G>A
AA Mutation	p.Arg925His(p.R925H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42693329:42693329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2785G>T
AA Mutation	p.Gly929Cys(p.G929C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42687789:42687789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1114G>A
AA Mutation	p.Val372Ile(p.V372I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42691448:42691448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2281G>A
AA Mutation	p.Asp761Asn(p.D761N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42687811:42687811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375309204
CDS Mutation	c.1136G>A
AA Mutation	p.Arg379His(p.R379H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42687814:42687814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763919892
CDS Mutation	c.1139G>A
AA Mutation	p.Arg380His(p.R380H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42691242:42691242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2165G>A
AA Mutation	p.Ser722Asn(p.S722N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42691962:42691962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142029931
CDS Mutation	c.2501G>A
AA Mutation	p.Arg834His(p.R834H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42696100:42696100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3422G>A
AA Mutation	p.Gly1141Asp(p.G1141D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42684155:42684155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.289G>A
AA Mutation	p.Val97Ile(p.V97I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42695826:42695826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3298G>C
AA Mutation	p.Val1100Leu(p.V1100L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42687772:42687772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097G>A
AA Mutation	p.Gly366Glu(p.G366E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42683890:42683890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137T>G
AA Mutation	p.Leu46Arg(p.L46R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42690110:42690110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1758G>T
AA Mutation	p.Glu586Asp(p.E586D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42691878:42691878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2417G>A
AA Mutation	p.Ser806Asn(p.S806N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42687880:42687880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1205G>A
AA Mutation	p.Arg402His(p.R402H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42685303:42685303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.598G>A
AA Mutation	p.Ala200Thr(p.A200T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42693438:42693438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760960237
CDS Mutation	c.2894G>A
AA Mutation	p.Arg965Gln(p.R965Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000264638
Start	42685357:42685357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652G>A
AA Mutation	p.Ala218Thr(p.A218T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264638
Start	42685017:42685017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264638
Start	42687890:42687890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1215C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264638
Start	42688586:42688586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1431G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264638
Start	42693400:42693400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577627164
CDS Mutation	c.2856T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264638
Start	42690134:42690134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753764412
CDS Mutation	c.1782T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264638
Start	42693417:42693417(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2873delC
AA Mutation	p.Thr958LysfsTer71(p.T958Kfs*71)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000264638
Start	42697661:42697661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775153843
CDS Mutation	c.3676C>T
AA Mutation	p.Arg1226Ter(p.R1226*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	29
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000264638
Start	42691993:42691993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2530+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	30
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000264638
Start	42691891:42691893(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2432_2434delTCT
AA Mutation	p.Phe811del(p.F811del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript