Mutation

Primary Site >> Stomach Cancer

Gene >> SPAG1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251809
Start	100225321:100225321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1837C>G
AA Mutation	p.Arg613Gly(p.R613G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000251809
Start	100194209:100194209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1037A>G
AA Mutation	p.Asn346Ser(p.N346S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000251809
Start	100162402:100162402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122A>C
AA Mutation	p.Lys41Thr(p.K41T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000251809
Start	100165971:100165971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298A>C
AA Mutation	p.Lys100Gln(p.K100Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000251809
Start	100231172:100231172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1872A>C
AA Mutation	p.Lys624Asn(p.K624N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000251809
Start	100225265:100225265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1781C>A
AA Mutation	p.Ala594Asp(p.A594D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000251809
Start	100165866:100165866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.193C>A
AA Mutation	p.Leu65Ile(p.L65I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000251809
Start	100191402:100191402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144608097
CDS Mutation	c.845G>A
AA Mutation	p.Arg282His(p.R282H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000251809
Start	100177918:100177918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.403A>C
AA Mutation	p.Asn135His(p.N135H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000251809
Start	100220322:100220322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777137396
CDS Mutation	c.1579C>T
AA Mutation	p.Arg527Trp(p.R527W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000251809
Start	100240992:100240992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2751A>G
AA Mutation	p.Ile917Met(p.I917M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000251809
Start	100240515:100240515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2393T>G
AA Mutation	p.Leu798Arg(p.L798R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000251809
Start	100220326:100220326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372376817
CDS Mutation	c.1583C>T
AA Mutation	p.Ala528Val(p.A528V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251809
Start	100183977:100183977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251809
Start	100240438:100240438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779086994
CDS Mutation	c.2316A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251809
Start	100183422:100183422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs74597335
CDS Mutation	c.474C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251809
Start	100194255:100194255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1083C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251809
Start	100194228:100194228(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1060delA
AA Mutation	p.Ser354AlafsTer36(p.S354Afs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000251809
Start	100241001:100241001(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2764delA
AA Mutation	p.Arg922GlyfsTer9(p.R922Gfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000251809
Start	100231290:100231290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1988+2C>T
Mutation Classification	Splice_Site
Feature Type	Transcript