Mutation

Primary Site >> Stomach Cancer

Gene >> SEMA6D

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47770510:47770510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1947A>C
AA Mutation	p.Glu649Asp(p.E649D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47763081:47763081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724G>A
AA Mutation	p.Val242Ile(p.V242I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47764970:47764970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1341G>A
AA Mutation	p.Met447Ile(p.M447I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47762260:47762260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.599G>A
AA Mutation	p.Arg200Gln(p.R200Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47761189:47761189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781098399
CDS Mutation	c.314G>A
AA Mutation	p.Arg105Gln(p.R105Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47765019:47765019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534298453
CDS Mutation	c.1390G>A
AA Mutation	p.Val464Ile(p.V464I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47771300:47771300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374871367
CDS Mutation	c.2737G>A
AA Mutation	p.Gly913Arg(p.G913R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47760984:47760984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.228A>C
AA Mutation	p.Gln76His(p.Q76H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47764979:47764979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1350A>T
AA Mutation	p.Lys450Asn(p.K450N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47771552:47771552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763608914
CDS Mutation	c.2989C>T
AA Mutation	p.Arg997Cys(p.R997C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47770887:47770887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2324A>G
AA Mutation	p.Glu775Gly(p.E775G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47764681:47764681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1141A>G
AA Mutation	p.Thr381Ala(p.T381A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47763028:47763028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671T>G
AA Mutation	p.Leu224Arg(p.L224R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47770929:47770929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2366A>G
AA Mutation	p.Lys789Arg(p.K789R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47764274:47764274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066G>A
AA Mutation	p.Ala356Thr(p.A356T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47771471:47771471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2908C>A
AA Mutation	p.Gln970Lys(p.Q970K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47771150:47771150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2587T>C
AA Mutation	p.Ser863Pro(p.S863P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47770929:47770929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2366A>C
AA Mutation	p.Lys789Thr(p.K789T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47764048:47764048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946T>C
AA Mutation	p.Phe316Leu(p.F316L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000316364
Start	47762287:47762287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626G>A
AA Mutation	p.Arg209His(p.R209H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316364
Start	47760320:47760320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750700486
CDS Mutation	c.126G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316364
Start	47771431:47771431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2868T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316364
Start	47770510:47770510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1947A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316364
Start	47771504:47771504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2941T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316364
Start	47764282:47764282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367727576
CDS Mutation	c.1074C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316364
Start	47771623:47771623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3060T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316364
Start	47759835:47759835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.37C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316364
Start	47770513:47770513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1950C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316364
Start	47764183:47764183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316364
Start	47763969:47763969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316364
Start	47763927:47763927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316364
Start	47762315:47762315(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.657delA
AA Mutation	p.Glu220SerfsTer8(p.E220Sfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316364
Start	47764746:47764747(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1206_1207insT
AA Mutation	p.Val403CysfsTer7(p.V403Cfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript