Mutation

Primary Site >> Stomach Cancer

Gene >> SMARCAD1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354268
Start	94278668:94278668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2231C>T
AA Mutation	p.Ser744Leu(p.S744L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354268
Start	94273672:94273672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1628G>A
AA Mutation	p.Gly543Asp(p.G543D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000354268
Start	94208530:94208530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.136G>C
AA Mutation	p.Glu46Gln(p.E46Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354268
Start	94240975:94240975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.674A>T
AA Mutation	p.Asp225Val(p.D225V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354268
Start	94264819:94264819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1394T>A
AA Mutation	p.Ile465Asn(p.I465N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000354268
Start	94280688:94280688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2515C>T
AA Mutation	p.His839Tyr(p.H839Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000354268
Start	94208453:94208453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749813218
CDS Mutation	c.59C>T
AA Mutation	p.Ala20Val(p.A20V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000354268
Start	94277040:94277040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1963C>T
AA Mutation	p.Leu655Phe(p.L655F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000354268
Start	94277043:94277043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1966A>C
AA Mutation	p.Thr656Pro(p.T656P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354268
Start	94252759:94252759(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs754697669
CDS Mutation	c.1040delA
AA Mutation	p.Asn347MetfsTer24(p.N347Mfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000354268
Start	94270813:94270813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1567G>T
AA Mutation	p.Glu523Ter(p.E523*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354268
Start	94252758:94252759(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1040dupA
AA Mutation	p.Asn347LysfsTer4(p.N347Kfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	13
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000354268
Start	94278614:94278614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2179-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript