Mutation

Primary Site >> Stomach Cancer

Gene >> MCM8

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5993666:5993666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147649536
CDS Mutation	c.2401C>T
AA Mutation	p.Arg801Trp(p.R801W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5952154:5952154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139C>A
AA Mutation	p.Arg47Ser(p.R47S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000378896
Start	5972009:5972009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771563950
CDS Mutation	c.1226C>T
AA Mutation	p.Ser409Leu(p.S409L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5963301:5963301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754811820
CDS Mutation	c.817T>C
AA Mutation	p.Ser273Pro(p.S273P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5963342:5963342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.858G>T
AA Mutation	p.Met286Ile(p.M286I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5952499:5952499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224A>G
AA Mutation	p.Tyr75Cys(p.Y75C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5967929:5967929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1127G>T
AA Mutation	p.Gly376Val(p.G376V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5952465:5952465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190T>C
AA Mutation	p.Ser64Pro(p.S64P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5993577:5993577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2312G>A
AA Mutation	p.Ser771Asn(p.S771N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5955157:5955157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138393496
CDS Mutation	c.392G>A
AA Mutation	p.Gly131Asp(p.G131D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000378896
Start	5983077:5983077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1645A>G
AA Mutation	p.Ser549Gly(p.S549G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378896
Start	5985988:5985988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2020C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378896
Start	5983100:5983100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1668T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378896
Start	5967936:5967936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378896
Start	5985999:5985999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2031G>A
Mutation Classification	Silent
Feature Type	Transcript