Colon Cancer: Gene >> MYBL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66592491:66592491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816G>T
AA Mutation	p.Glu272Asp(p.E272D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66597396:66597396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745341038
CDS Mutation	c.446T>C
AA Mutation	p.Ile149Thr(p.I149T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66576176:66576176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1301C>A
AA Mutation	p.Ser434Tyr(p.S434Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66576104:66576104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767661399
CDS Mutation	c.1373C>T
AA Mutation	p.Ser458Phe(p.S458F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66580324:66580324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.910G>T
AA Mutation	p.Asp304Tyr(p.D304Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66573488:66573488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1489G>T
AA Mutation	p.Gly497Cys(p.G497C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66602492:66602492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763361530
CDS Mutation	c.52G>A
AA Mutation	p.Asp18Asn(p.D18N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66597364:66597364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.478C>A
AA Mutation	p.Arg160Ser(p.R160S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66566111:66566111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2083C>T
AA Mutation	p.Pro695Ser(p.P695S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66576215:66576215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1262C>A
AA Mutation	p.Thr421Asn(p.T421N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66597340:66597340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502C>T
AA Mutation	p.Leu168Phe(p.L168F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66572525:66572525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770108773
CDS Mutation	c.1685C>T
AA Mutation	p.Ala562Val(p.A562V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000522677
Start	66566705:66566705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1929T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000522677
Start	66576218:66576218(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1259delA
AA Mutation	p.Asn420ThrfsTer13(p.N420Tfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000522677
Start	66595597:66595597(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.673delT
AA Mutation	p.Tyr225ThrfsTer19(p.Y225Tfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000522677
Start	66597524:66597524(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.318delG
AA Mutation	p.Pro107GlnfsTer6(p.P107Qfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000522677
Start	66599115:66599115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226C>T
AA Mutation	p.Arg76Ter(p.R76*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000522677
Start	66566944:66566945(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1776dupA
AA Mutation	p.Glu593ArgfsTer14(p.E593Rfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MYBL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66599139:66599139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202C>T
AA Mutation	p.Arg68Cys(p.R68C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66566119:66566119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2075A>C
AA Mutation	p.Lys692Thr(p.K692T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000522677
Start	66597423:66597423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419C>A
AA Mutation	p.Ser140Tyr(p.S140Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000522677
Start	66592512:66592512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000522677
Start	66580289:66580289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565495156
CDS Mutation	c.945C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000522677
Start	66595717:66595717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.553C>T
AA Mutation	p.Arg185Ter(p.R185*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000522677
Start	66576005:66576005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1470+2T>G
Mutation Classification	Splice_Site
Feature Type	Transcript