Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MEMO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295065
Start	31869901:31869901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.709A>C
AA Mutation	p.Lys237Gln(p.K237Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295065
Start	31932121:31932121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158C>T
AA Mutation	p.Thr53Met(p.T53M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295065
Start	31869906:31869906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704A>G
AA Mutation	p.Tyr235Cys(p.Y235C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295065
Start	31932075:31932075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140215147
CDS Mutation	c.204G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295065
Start	31868430:31868430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000295065
Start	31868460:31868461(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.794_795insAGTTC
AA Mutation	p.Asn265LysfsTer4(p.N265Kfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000295065
Start	31883385:31883385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MEMO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295065
Start	31868428:31868428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771196397
CDS Mutation	c.827C>T
AA Mutation	p.Ser276Leu(p.S276L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295065
Start	31892028:31892028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544A>C
AA Mutation	p.Asn182His(p.N182H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295065
Start	31868455:31868455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.800G>A
AA Mutation	p.Ser267Asn(p.S267N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000295065
Start	31932066:31932066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript