Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> JARID2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15497011:15497011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781217563
CDS Mutation	c.1786C>T
AA Mutation	p.Arg596Trp(p.R596W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15487382:15487382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.746C>T
AA Mutation	p.Ala249Val(p.A249V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15496435:15496435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751363793
CDS Mutation	c.1210G>A
AA Mutation	p.Val404Ile(p.V404I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15501255:15501255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202079041
CDS Mutation	c.2294C>T
AA Mutation	p.Ala765Val(p.A765V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15496957:15496957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759192312
CDS Mutation	c.1732C>T
AA Mutation	p.Arg578Cys(p.R578C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15501360:15501360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781115380
CDS Mutation	c.2399A>G
AA Mutation	p.Glu800Gly(p.E800G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15520171:15520171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373598286
CDS Mutation	c.3661C>T
AA Mutation	p.Arg1221Cys(p.R1221C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15500981:15500981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2020C>T
AA Mutation	p.Leu674Phe(p.L674F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15512248:15512248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2993A>G
AA Mutation	p.His998Arg(p.H998R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15513259:15513259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772155471
CDS Mutation	c.3287G>A
AA Mutation	p.Arg1096His(p.R1096H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15496678:15496678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746629156
CDS Mutation	c.1453G>A
AA Mutation	p.Val485Met(p.V485M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15512308:15512308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3053A>T
AA Mutation	p.Lys1018Ile(p.K1018I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15520087:15520087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3577G>A
AA Mutation	p.Val1193Ile(p.V1193I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15513006:15513006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3227C>G
AA Mutation	p.Pro1076Arg(p.P1076R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15511396:15511396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751270951
CDS Mutation	c.2947G>A
AA Mutation	p.Val983Ile(p.V983I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341776
Start	15496254:15496254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777430988
CDS Mutation	c.1029G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341776
Start	15496722:15496722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201664236
CDS Mutation	c.1497G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341776
Start	15487473:15487473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142545160
CDS Mutation	c.837G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341776
Start	15496413:15496413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149943687
CDS Mutation	c.1188G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341776
Start	15501250:15501250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750878402
CDS Mutation	c.2289C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341776
Start	15512989:15512989(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3216delA
AA Mutation	p.Glu1073LysfsTer106(p.E1073Kfs*106)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341776
Start	15496995:15496995(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1775delC
AA Mutation	p.Pro592LeufsTer57(p.P592Lfs*57)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341776
Start	15496405:15496405(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1186delG
AA Mutation	p.Ala396ArgfsTer18(p.A396Rfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000341776
Start	15520223:15520223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3713C>A
AA Mutation	p.Ser1238Ter(p.S1238*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000341776
Start	15452172:15452172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371399734
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Ter(p.R164*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341776
Start	15500983:15500984(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2028dupA
AA Mutation	p.Trp677MetfsTer133(p.W677Mfs*133)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> JARID2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15501219:15501219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2258G>C
AA Mutation	p.Arg753Pro(p.R753P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15501030:15501030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2069C>A
AA Mutation	p.Ala690Asp(p.A690D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341776
Start	15504558:15504558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2507G>C
AA Mutation	p.Cys836Ser(p.C836S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341776
Start	15496947:15496947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1722C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000341776
Start	15452172:15452172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371399734
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Ter(p.R164*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000341776
Start	15452177:15452177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript