Mutation

Primary Site >> Stomach Cancer

Gene >> MOS

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113888:56113888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95C>T
AA Mutation	p.Ala32Val(p.A32V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113261:56113261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.722G>A
AA Mutation	p.Gly241Asp(p.G241D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113078:56113078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905C>T
AA Mutation	p.Ala302Val(p.A302V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113921:56113921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.62C>T
AA Mutation	p.Ala21Val(p.A21V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113736:56113736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.247C>T
AA Mutation	p.Pro83Ser(p.P83S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113076:56113076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907G>A
AA Mutation	p.Val303Ile(p.V303I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113153:56113153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830C>T
AA Mutation	p.Ala277Val(p.A277V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113702:56113702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281A>C
AA Mutation	p.Lys94Thr(p.K94T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113603:56113603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380C>T
AA Mutation	p.Thr127Met(p.T127M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113574:56113574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.409A>C
AA Mutation	p.Ile137Leu(p.I137L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113606:56113606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377G>A
AA Mutation	p.Arg126His(p.R126H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000311923
Start	56113445:56113445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773486880
CDS Mutation	c.538A>G
AA Mutation	p.Lys180Glu(p.K180E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311923
Start	56113239:56113239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.744G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311923
Start	56113524:56113524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311923
Start	56113608:56113608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311923
Start	56113218:56113218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000311923
Start	56113333:56113334(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.649dupA
AA Mutation	p.Ile217AsnfsTer2(p.I217Nfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript