Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> YLPM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74778507:74778507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934C>A
AA Mutation	p.His312Asn(p.H312N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74798787:74798787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760862932
CDS Mutation	c.3490C>T
AA Mutation	p.Arg1164Cys(p.R1164C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74810266:74810266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190418068
CDS Mutation	c.5074C>T
AA Mutation	p.Arg1692Cys(p.R1692C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74764175:74764175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686A>G
AA Mutation	p.Gln229Arg(p.Q229R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74809964:74809964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4994G>A
AA Mutation	p.Arg1665His(p.R1665H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74778525:74778525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.952A>C
AA Mutation	p.Lys318Gln(p.K318Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74798671:74798671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3374T>C
AA Mutation	p.Leu1125Pro(p.L1125P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74829269:74829269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6220G>A
AA Mutation	p.Ala2074Thr(p.A2074T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74781358:74781358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1315C>T
AA Mutation	p.Arg439Trp(p.R439W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74809591:74809591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4733C>A
AA Mutation	p.Ser1578Tyr(p.S1578Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74817078:74817078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5833T>C
AA Mutation	p.Trp1945Arg(p.W1945R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74799495:74799495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200748724
CDS Mutation	c.4198C>T
AA Mutation	p.Arg1400Trp(p.R1400W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74812706:74812706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5426G>T
AA Mutation	p.Arg1809Leu(p.R1809L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74781458:74781458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1415A>C
AA Mutation	p.Lys472Thr(p.K472T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74797690:74797690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2393A>G
AA Mutation	p.Glu798Gly(p.E798G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74812757:74812757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776882142
CDS Mutation	c.5477C>T
AA Mutation	p.Pro1826Leu(p.P1826L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74835395:74835395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758625730
CDS Mutation	c.6425G>A
AA Mutation	p.Arg2142Gln(p.R2142Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74764000:74764000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511C>A
AA Mutation	p.Pro171Thr(p.P171T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325680
Start	74763849:74763849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325680
Start	74812740:74812740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372350383
CDS Mutation	c.5460C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325680
Start	74809502:74809502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4644A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325680
Start	74798741:74798741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3444A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325680
Start	74781699:74781699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1656T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325680
Start	74798057:74798057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2760G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325680
Start	74781801:74781801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1758G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325680
Start	74781355:74781355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1312C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325680
Start	74798830:74798830(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3538delA
AA Mutation	p.Met1180CysfsTer27(p.M1180Cfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325680
Start	74764244:74764244(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.761delC
AA Mutation	p.Pro254LeufsTer35(p.P254Lfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325680
Start	74811671:74811671(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5283delT
AA Mutation	p.Phe1761LeufsTer40(p.F1761Lfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325680
Start	74797738:74797738(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2445delG
AA Mutation	p.Pro816GlnfsTer13(p.P816Qfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000325680
Start	74810311:74810311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5119C>T
AA Mutation	p.Arg1707Ter(p.R1707*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000325680
Start	74798016:74798016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2719C>T
AA Mutation	p.Gln907Ter(p.Q907*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000325680
Start	74811633:74811633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5242C>T
AA Mutation	p.Arg1748Ter(p.R1748*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	stop_gained
Transcription ID	ENST00000325680
Start	74798706:74798706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3409C>T
AA Mutation	p.Arg1137Ter(p.R1137*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> YLPM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74816934:74816934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564314857
CDS Mutation	c.5689A>G
AA Mutation	p.Met1897Val(p.M1897V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74799254:74799254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3957A>C
AA Mutation	p.Gln1319His(p.Q1319H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74799551:74799551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4254A>C
AA Mutation	p.Glu1418Asp(p.E1418D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74798205:74798205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2908G>C
AA Mutation	p.Ala970Pro(p.A970P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74798469:74798469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201838422
CDS Mutation	c.3172C>T
AA Mutation	p.Arg1058Trp(p.R1058W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325680
Start	74809642:74809642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4784T>G
AA Mutation	p.Phe1595Cys(p.F1595C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325680
Start	74780536:74780536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000325680
Start	74816263:74816263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5563C>T
AA Mutation	p.Arg1855Ter(p.R1855*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000325680
Start	74799366:74799366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4069C>T
AA Mutation	p.Arg1357Ter(p.R1357*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript