Colon Cancer: Gene >> DAB2IP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000408936
Start	121773260:121773260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2732C>T
AA Mutation	p.Ala911Val(p.A911V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000408936
Start	121760293:121760293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1024A>G
AA Mutation	p.Met342Val(p.M342V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259371
Start	121567204:121567204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.16C>A
AA Mutation	p.Leu6Ile(p.L6I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000408936
Start	121766505:121766505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1472G>A
AA Mutation	p.Arg491Gln(p.R491Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000408936
Start	121760024:121760024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755A>G
AA Mutation	p.Asp252Gly(p.D252G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000408936
Start	121773002:121773002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2474C>T
AA Mutation	p.Pro825Leu(p.P825L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000408936
Start	121768578:121768578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774832244
CDS Mutation	c.1844G>A
AA Mutation	p.Arg615His(p.R615H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000408936
Start	121768502:121768502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766959002
CDS Mutation	c.1768C>T
AA Mutation	p.Arg590Cys(p.R590C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000408936
Start	121782368:121782368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750277403
CDS Mutation	c.3440G>A
AA Mutation	p.Arg1147His(p.R1147H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000408936
Start	121758974:121758974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368193656
CDS Mutation	c.593G>A
AA Mutation	p.Arg198Gln(p.R198Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000408936
Start	121678765:121678765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199540285
CDS Mutation	c.212C>T
AA Mutation	p.Thr71Met(p.T71M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000408936
Start	121760129:121760129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746510057
CDS Mutation	c.860G>A
AA Mutation	p.Arg287His(p.R287H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408936
Start	121773165:121773165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368800049
CDS Mutation	c.2637G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408936
Start	121782348:121782348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753664017
CDS Mutation	c.3420G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408936
Start	121782468:121782468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408936
Start	121774325:121774325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371735785
CDS Mutation	c.3033G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408936
Start	121763642:121763642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149420814
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408936
Start	121699375:121699375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.279G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408936
Start	121757133:121757133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408936
Start	121773142:121773142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2614C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000408936
Start	121773334:121773334(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2811delC
AA Mutation	p.Asn938ThrfsTer3(p.N938Tfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000408936
Start	121772659:121772659(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2136delT
AA Mutation	p.Phe712LeufsTer81(p.F712Lfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DAB2IP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000408936
Start	121782370:121782370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3442C>T
AA Mutation	p.Leu1148Phe(p.L1148F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408936
Start	121766530:121766530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371966536
CDS Mutation	c.1497G>A
Mutation Classification	Silent
Feature Type	Transcript