Mutation

Primary Site >> Stomach Cancer

Gene >> CACNA2D3

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54642186:54642186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1112G>A
AA Mutation	p.Gly371Glu(p.G371E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54503501:54503501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.391T>G
AA Mutation	p.Phe131Val(p.F131V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54562821:54562821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.566T>G
AA Mutation	p.Val189Gly(p.V189G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54123578:54123578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188C>T
AA Mutation	p.Ser63Phe(p.S63F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54562918:54562918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663T>A
AA Mutation	p.Phe221Leu(p.F221L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54984630:54984630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2579A>G
AA Mutation	p.Asp860Gly(p.D860G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54888013:54888013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2111T>A
AA Mutation	p.Ile704Asn(p.I704N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	55073792:55073792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3116A>C
AA Mutation	p.Lys1039Thr(p.K1039T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54871606:54871606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1694A>G
AA Mutation	p.Glu565Gly(p.E565G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54896761:54896761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2259A>T
AA Mutation	p.Lys753Asn(p.K753N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54896846:54896846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2344G>C
AA Mutation	p.Val782Leu(p.V782L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	55004801:55004801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2729A>C
AA Mutation	p.Asn910Thr(p.N910T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54838623:54838623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1526T>G
AA Mutation	p.Leu509Arg(p.L509R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54879052:54879052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1745A>C
AA Mutation	p.Lys582Thr(p.K582T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	55004810:55004810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2738G>A
AA Mutation	p.Ser913Asn(p.S913N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54891389:54891389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2185G>A
AA Mutation	p.Gly729Ser(p.G729S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000288197
Start	54871620:54871620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764866239
CDS Mutation	c.1708G>A
AA Mutation	p.Val570Met(p.V570M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54764280:54764280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752111419
CDS Mutation	c.1309G>A
AA Mutation	p.Val437Met(p.V437M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	55004815:55004815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775717340
CDS Mutation	c.2743G>A
AA Mutation	p.Asp915Asn(p.D915N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000288197
Start	54885493:54885493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1963T>C
AA Mutation	p.Tyr655His(p.Y655H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288197
Start	54837224:54837224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1464C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288197
Start	54880808:54880808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745684927
CDS Mutation	c.1857G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288197
Start	54123576:54123576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288197
Start	54123531:54123531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288197
Start	55073448:55073448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2991C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288197
Start	54570038:54570038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748264157
CDS Mutation	c.822C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288197
Start	54627825:54627825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1002A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000288197
Start	55004820:55004820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763097870
CDS Mutation	c.2748C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000288197
Start	54562913:54562913(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.663delT
AA Mutation	p.Phe221LeufsTer40(p.F221Lfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000288197
Start	54871557:54871557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645C>T
AA Mutation	p.Arg549Ter(p.R549*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000288197
Start	54764256:54764256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1285G>T
AA Mutation	p.Glu429Ter(p.E429*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000288197
Start	54569848:54569848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730C>T
AA Mutation	p.Arg244Ter(p.R244*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	33
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000288197
Start	54899787:54899787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2369-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript