Mutation

Primary Site >> Stomach Cancer

Gene >> MED23

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368068
Start	131594215:131594215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376944115
CDS Mutation	c.3116C>T
AA Mutation	p.Pro1039Leu(p.P1039L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368068
Start	131594252:131594252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3079G>A
AA Mutation	p.Val1027Ile(p.V1027I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368068
Start	131596072:131596072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2870G>T
AA Mutation	p.Gly957Val(p.G957V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368068
Start	131621932:131621932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444T>G
AA Mutation	p.Ile148Met(p.I148M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368068
Start	131590341:131590341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3788G>T
AA Mutation	p.Arg1263Ile(p.R1263I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368068
Start	131623448:131623448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299C>T
AA Mutation	p.Ser100Phe(p.S100F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000368068
Start	131598556:131598556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2426G>T
AA Mutation	p.Arg809Ile(p.R809I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368068
Start	131594162:131594162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3169G>A
AA Mutation	p.Glu1057Lys(p.E1057K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368068
Start	131606513:131606513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1333A>T
AA Mutation	p.Ile445Phe(p.I445F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368068
Start	131602325:131602325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372590711
CDS Mutation	c.1988C>T
AA Mutation	p.Pro663Leu(p.P663L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368068
Start	131593113:131593113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3291T>A
AA Mutation	p.Phe1097Leu(p.F1097L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000368068
Start	131593076:131593076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3328G>A
AA Mutation	p.Val1110Met(p.V1110M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000368068
Start	131590335:131590335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770824001
CDS Mutation	c.3794G>A
AA Mutation	p.Arg1265His(p.R1265H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368068
Start	131608045:131608045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1104C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368068
Start	131598413:131598413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2481A>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368068
Start	131598618:131598618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2364C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368068
Start	131619834:131619834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.660C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368068
Start	131591489:131591489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3510T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368068
Start	131623405:131623405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.342T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368068
Start	131596018:131596018(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2924delT
AA Mutation	p.Leu975Ter(p.L975*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368068
Start	131600155:131600155(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2103delT
AA Mutation	p.Phe701LeufsTer20(p.F701Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368068
Start	131623364:131623364(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.383delG
AA Mutation	p.Gly128GlufsTer11(p.G128Efs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368068
Start	131598706:131598706(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2276delA
AA Mutation	p.Asn759MetfsTer12(p.N759Mfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368068
Start	131627409:131627409(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.146delG
AA Mutation	p.Gly49ValfsTer35(p.G49Vfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368068
Start	131589535:131589539(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3865_3869delAATTA
AA Mutation	p.Asn1289HisfsTer6(p.N1289Hfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000368068
Start	131607988:131607989(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1160dupA
AA Mutation	p.Asn387LysfsTer5(p.N387Kfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	27
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000368068
Start	131598468:131598468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2427-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript