Mutation

Primary Site >> Stomach Cancer

Gene >> MTNR1A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307161
Start	186533732:186533732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1010C>A
AA Mutation	p.Pro337Gln(p.P337Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307161
Start	186533723:186533723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019C>A
AA Mutation	p.Thr340Asn(p.T340N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307161
Start	186533946:186533946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148793802
CDS Mutation	c.796G>A
AA Mutation	p.Ala266Thr(p.A266T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307161
Start	186534285:186534285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457C>T
AA Mutation	p.Leu153Phe(p.L153F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307161
Start	186533964:186533964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.778G>A
AA Mutation	p.Ala260Thr(p.A260T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307161
Start	186534368:186534368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.374G>A
AA Mutation	p.Arg125His(p.R125H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307161
Start	186533716:186533716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307161
Start	186533806:186533806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202137339
CDS Mutation	c.936G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307161
Start	186534481:186534481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773877086
CDS Mutation	c.261G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307161
Start	186534417:186534417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307161
Start	186534208:186534208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.534C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307161
Start	186534001:186534001(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.741delT
AA Mutation	p.Phe247LeufsTer8(p.F247Lfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript