Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MEIS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	37093715:37093715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.505G>A
AA Mutation	p.Asp169Asn(p.D169N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	36892241:36892241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1366A>C
AA Mutation	p.Ser456Arg(p.S456R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	36892247:36892247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1360G>A
AA Mutation	p.Ala454Thr(p.A454T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	37098054:37098054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.158C>T
AA Mutation	p.Ala53Val(p.A53V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	37098121:37098121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.91C>T
AA Mutation	p.Arg31Trp(p.R31W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	37093724:37093724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496G>A
AA Mutation	p.Glu166Lys(p.E166K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	36892429:36892429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1178C>A
AA Mutation	p.Ser393Tyr(p.S393Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	36896655:36896655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009C>T
AA Mutation	p.Pro337Ser(p.P337S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000561208
Start	37036904:37036904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183075611
CDS Mutation	c.810G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000561208
Start	37096331:37096331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.345C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000561208
Start	37036889:37036889(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.825delA
AA Mutation	p.Lys275AsnfsTer12(p.K275Nfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000561208
Start	37098108:37098108(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.104delC
AA Mutation	p.Pro35ArgfsTer5(p.P35Rfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000561208
Start	37096425:37096425(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.251delC
AA Mutation	p.Pro84ArgfsTer6(p.P84Rfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MEIS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	37093664:37093664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.556G>A
AA Mutation	p.Asp186Asn(p.D186N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	36892202:36892202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760342372
CDS Mutation	c.1405G>A
AA Mutation	p.Gly469Arg(p.G469R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	37095605:37095605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.397G>A
AA Mutation	p.Glu133Lys(p.E133K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	37036887:37036887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767585793
CDS Mutation	c.827G>A
AA Mutation	p.Arg276His(p.R276H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000561208
Start	36892222:36892222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1385C>A
AA Mutation	p.Ser462Tyr(p.S462Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000561208
Start	36950350:36950350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.951A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000561208
Start	37098044:37098044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000561208
Start	37099458:37099458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.9A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000561208
Start	36896634:36896634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030C>T
AA Mutation	p.Arg344Ter(p.R344*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript