Mutation

Primary Site >> Stomach Cancer

Gene >> MEIS1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66568737:66568737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1095T>G
AA Mutation	p.His365Gln(p.H365Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66439910:66439910(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.307G>A
AA Mutation	p.Glu103Lys(p.E103K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66547977:66547977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.923T>C
AA Mutation	p.Leu308Ser(p.L308S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66437902:66437902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.178G>C
AA Mutation	p.Ala60Pro(p.A60P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66439967:66439967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364G>A
AA Mutation	p.Ala122Thr(p.A122T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66569097:66569097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1162C>T
AA Mutation	p.His388Tyr(p.H388Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66512221:66512221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61752693
CDS Mutation	c.815G>A
AA Mutation	p.Arg272His(p.R272H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66569099:66569099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1164C>G
AA Mutation	p.His388Gln(p.H388Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000272369
Start	66437827:66437827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.103C>T
AA Mutation	p.Pro35Ser(p.P35S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272369
Start	66512210:66512210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272369
Start	66569102:66569102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1167C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000272369
Start	66439939:66439939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript