Mutation

Primary Site >> Stomach Cancer

Gene >> ARMC4

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000305242
Start	27944817:27944817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1532A>G
AA Mutation	p.Lys511Arg(p.K511R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27935214:27935214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2291T>G
AA Mutation	p.Leu764Arg(p.L764R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27981491:27981491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911A>C
AA Mutation	p.Lys304Thr(p.K304T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27935201:27935201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2304G>T
AA Mutation	p.Gln768His(p.Q768H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27907752:27907752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749218788
CDS Mutation	c.2521C>T
AA Mutation	p.Arg841Cys(p.R841C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27935247:27935247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760325470
CDS Mutation	c.2258G>A
AA Mutation	p.Arg753Gln(p.R753Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27981489:27981489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913T>G
AA Mutation	p.Phe305Val(p.F305V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27944287:27944287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773935799
CDS Mutation	c.1678G>A
AA Mutation	p.Ala560Thr(p.A560T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27944296:27944296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145742175
CDS Mutation	c.1669G>A
AA Mutation	p.Glu557Lys(p.E557K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27860666:27860666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369022423
CDS Mutation	c.2980G>A
AA Mutation	p.Ala994Thr(p.A994T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27907767:27907767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369264618
CDS Mutation	c.2506C>T
AA Mutation	p.Arg836Cys(p.R836C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27961671:27961671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138508233
CDS Mutation	c.1283C>T
AA Mutation	p.Ser428Leu(p.S428L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27985116:27985116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750563454
CDS Mutation	c.478G>C
AA Mutation	p.Asp160His(p.D160H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000305242
Start	27862519:27862519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2714T>G
AA Mutation	p.Ile905Ser(p.I905S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305242
Start	27971266:27971266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.984C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305242
Start	27939924:27939924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2070G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305242
Start	27944240:27944240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761710990
CDS Mutation	c.1725C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305242
Start	27995095:27995095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305242
Start	27936784:27936784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2194T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305242
Start	27944927:27944927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1422T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305242
Start	27944235:27944235(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1730delG
AA Mutation	p.Gly577ValfsTer9(p.G577Vfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000305242
Start	27995049:27995049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94A>T
AA Mutation	p.Lys32Ter(p.K32*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000305242
Start	27907758:27907758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2515G>T
AA Mutation	p.Gly839Ter(p.G839*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000305242
Start	27985158:27985158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436G>T
AA Mutation	p.Glu146Ter(p.E146*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	25
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000305242
Start	27936725:27936725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2252+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript