Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MORC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109099444:109099444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781262820
CDS Mutation	c.337G>T
AA Mutation	p.Asp113Tyr(p.D113Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109103896:109103896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.176G>A
AA Mutation	p.Gly59Glu(p.G59E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109007084:109007084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1712T>G
AA Mutation	p.Phe571Cys(p.F571C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109035448:109035448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1351T>C
AA Mutation	p.Phe451Leu(p.F451L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109069638:109069638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.809G>A
AA Mutation	p.Arg270Lys(p.R270K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109063224:109063224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.823C>A
AA Mutation	p.Leu275Ile(p.L275I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109094959:109094959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.533A>C
AA Mutation	p.Lys178Thr(p.K178T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	108979617:108979617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2375C>T
AA Mutation	p.Ala792Val(p.A792V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000232603
Start	109095067:109095067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.425T>C
AA Mutation	p.Val142Ala(p.V142A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109094989:109094989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.503T>C
AA Mutation	p.Leu168Ser(p.L168S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109057466:109057466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762063643
CDS Mutation	c.1052C>T
AA Mutation	p.Thr351Met(p.T351M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	108984758:108984758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2282T>C
AA Mutation	p.Val761Ala(p.V761A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232603
Start	108979652:108979652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs75923723
CDS Mutation	c.2340G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232603
Start	109057441:109057441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369056513
CDS Mutation	c.1077C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232603
Start	109100440:109100440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232603
Start	109027868:109027868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1587A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232603
Start	109035416:109035416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758284901
CDS Mutation	c.1383C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232603
Start	109069748:109069748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145046251
CDS Mutation	c.699G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232603
Start	109100431:109100431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232603
Start	108979577:108979577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777002185
CDS Mutation	c.2415G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	108986903:108986903(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2234delA
AA Mutation	p.Lys745ArgfsTer6(p.K745Rfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	109099393:109099393(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.388delT
AA Mutation	p.Ser130LeufsTer14(p.S130Lfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	109103904:109103904(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.168delA
AA Mutation	p.Lys56AsnfsTer17(p.K56Nfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	109103893:109103893(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.179delG
AA Mutation	p.Gly60AspfsTer13(p.G60Dfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	108958986:108958987(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2933dupA
AA Mutation	p.Asn978LysfsTer2(p.N978Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000232603
Start	109035468:109035469(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1331-1_1331insTAATT
AA Mutation	p.Asn444IlefsTer7(p.N444Ifs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MORC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109094977:109094977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.515A>T
AA Mutation	p.Tyr172Phe(p.Y172F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	108986936:108986936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2201G>T
AA Mutation	p.Ser734Ile(p.S734I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109118019:109118019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759790452
CDS Mutation	c.41G>A
AA Mutation	p.Arg14His(p.R14H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	108963579:108963579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2634A>C
AA Mutation	p.Glu878Asp(p.E878D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109004882:109004882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2020C>A
AA Mutation	p.Gln674Lys(p.Q674K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109057430:109057430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201598350
CDS Mutation	c.1088G>A
AA Mutation	p.Arg363Gln(p.R363Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109059826:109059826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564959353
CDS Mutation	c.1011G>T
AA Mutation	p.Lys337Asn(p.K337N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000232603
Start	109099444:109099444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781262820
CDS Mutation	c.337G>T
AA Mutation	p.Asp113Tyr(p.D113Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232603
Start	108963462:108963462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2751G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232603
Start	108979571:108979571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543158461
CDS Mutation	c.2421G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232603
Start	108963478:108963479(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2734_2735insC
AA Mutation	p.Ile912ThrfsTer3(p.I912Tfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000232603
Start	108959121:108959121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2800-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript