Colon Cancer: Gene >> MIB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21741706:21741706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123C>A
AA Mutation	p.Ser41Arg(p.S41R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21844111:21844111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760875023
CDS Mutation	c.2069C>T
AA Mutation	p.Ala690Val(p.A690V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21798103:21798103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376378881
CDS Mutation	c.1112G>A
AA Mutation	p.Arg371Gln(p.R371Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21791415:21791415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950T>C
AA Mutation	p.Val317Ala(p.V317A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21779552:21779552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775G>A
AA Mutation	p.Glu259Lys(p.E259K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21773666:21773666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771020731
CDS Mutation	c.574G>A
AA Mutation	p.Ala192Thr(p.A192T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21838468:21838468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1933G>T
AA Mutation	p.Val645Leu(p.V645L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261537
Start	21803921:21803921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1386T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261537
Start	21847057:21847057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781491471
CDS Mutation	c.2325G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000261537
Start	21857165:21857165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369135845
CDS Mutation	c.2701C>T
AA Mutation	p.Arg901Ter(p.R901*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000261537
Start	21791504:21791504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376597435
CDS Mutation	c.1039C>T
AA Mutation	p.Arg347Ter(p.R347*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MIB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21798184:21798184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1193C>T
AA Mutation	p.Ser398Phe(p.S398F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21819519:21819519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1702C>A
AA Mutation	p.His568Asn(p.H568N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21768719:21768719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498A>T
AA Mutation	p.Glu166Asp(p.E166D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21849236:21849236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2434G>T
AA Mutation	p.Asp812Tyr(p.D812Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21864652:21864652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150652745
CDS Mutation	c.3007A>G
AA Mutation	p.Ile1003Val(p.I1003V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21779552:21779552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775G>A
AA Mutation	p.Glu259Lys(p.E259K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21849324:21849324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2522C>A
AA Mutation	p.Ser841Tyr(p.S841Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261537
Start	21791418:21791418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746365974
CDS Mutation	c.953G>A
AA Mutation	p.Arg318Gln(p.R318Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261537
Start	21857227:21857227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2763T>C
Mutation Classification	Silent
Feature Type	Transcript