Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> AMOTL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94859560:94859560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1980A>C
AA Mutation	p.Glu660Asp(p.E660D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94869449:94869449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2740G>T
AA Mutation	p.Ala914Ser(p.A914S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94800205:94800205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015C>A
AA Mutation	p.Pro339Thr(p.P339T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94869398:94869398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750475731
CDS Mutation	c.2689G>A
AA Mutation	p.Gly897Ser(p.G897S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94799887:94799887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.697A>G
AA Mutation	p.Arg233Gly(p.R233G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94821600:94821600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756534459
CDS Mutation	c.1192G>A
AA Mutation	p.Ala398Thr(p.A398T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94869380:94869380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2671G>A
AA Mutation	p.Ala891Thr(p.A891T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94866002:94866002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2322G>C
AA Mutation	p.Gln774His(p.Q774H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94853937:94853937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1799G>A
AA Mutation	p.Arg600Gln(p.R600Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94869291:94869291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764026403
CDS Mutation	c.2582C>T
AA Mutation	p.Thr861Met(p.T861M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94859592:94859592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376912369
CDS Mutation	c.2012G>A
AA Mutation	p.Arg671Gln(p.R671Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94864761:94864761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762133686
CDS Mutation	c.2162G>A
AA Mutation	p.Arg721Gln(p.R721Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94799746:94799746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.556G>A
AA Mutation	p.Glu186Lys(p.E186K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94799921:94799921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371806495
CDS Mutation	c.731C>T
AA Mutation	p.Ala244Val(p.A244V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94799408:94799408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.218A>C
AA Mutation	p.Asn73Thr(p.N73T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94799491:94799491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301C>T
AA Mutation	p.Arg101Trp(p.R101W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000433060
Start	94850114:94850114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1649A>G
AA Mutation	p.Asn550Ser(p.N550S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94800220:94800220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1030G>A
AA Mutation	p.Glu344Lys(p.E344K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94831496:94831496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1603G>A
AA Mutation	p.Glu535Lys(p.E535K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94869359:94869359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771639549
CDS Mutation	c.2650G>A
AA Mutation	p.Glu884Lys(p.E884K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94799669:94799669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479C>T
AA Mutation	p.Pro160Leu(p.P160L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94853940:94853940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1802A>G
AA Mutation	p.Glu601Gly(p.E601G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94859627:94859627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752948602
CDS Mutation	c.2047G>A
AA Mutation	p.Asp683Asn(p.D683N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94795107:94795107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.146A>G
AA Mutation	p.His49Arg(p.H49R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433060
Start	94800177:94800177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.987G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433060
Start	94799892:94799892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.702C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433060
Start	94799622:94799622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433060
Start	94821677:94821677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776044957
CDS Mutation	c.1269C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433060
Start	94795105:94795105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433060
Start	94864774:94864774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773589464
CDS Mutation	c.2175C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433060
Start	94869412:94869412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755363731
CDS Mutation	c.2703G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433060
Start	94869283:94869283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2574C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433060
Start	94799412:94799412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000433060
Start	94800064:94800064(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.879delG
AA Mutation	p.Ser295ProfsTer26(p.S295Pfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000433060
Start	94800289:94800289(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1103delC
AA Mutation	p.Pro368LeufsTer5(p.P368Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000433060
Start	94800185:94800185(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1000delT
AA Mutation	p.Tyr334MetfsTer22(p.Y334Mfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	stop_gained
Transcription ID	ENST00000433060
Start	94850119:94850119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1654G>T
AA Mutation	p.Glu552Ter(p.E552*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	stop_gained
Transcription ID	ENST00000433060
Start	94795122:94795122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161T>A
AA Mutation	p.Leu54Ter(p.L54*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> AMOTL1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000433060
Start	94869471:94869471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2762T>A
AA Mutation	p.Leu921Gln(p.L921Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94859607:94859607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770787342
CDS Mutation	c.2027G>A
AA Mutation	p.Arg676Gln(p.R676Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94831455:94831455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1562G>A
AA Mutation	p.Arg521Gln(p.R521Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94799876:94799876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686G>A
AA Mutation	p.Arg229Gln(p.R229Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000433060
Start	94869461:94869461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs77127753
CDS Mutation	c.2752G>A
AA Mutation	p.Ala918Thr(p.A918T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000433060
Start	94831540:94831540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1647G>T
AA Mutation	p.Gln549His(p.Q549H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000433060
Start	94864744:94864744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2145G>A
Mutation Classification	Silent
Feature Type	Transcript