Colon Cancer: Gene >> LMO7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75841932:75841932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148659145
CDS Mutation	c.3281G>A
AA Mutation	p.Arg1094His(p.R1094H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75841149:75841149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2924G>T
AA Mutation	p.Trp975Leu(p.W975L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000465261
Start	75835338:75835338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2633C>A
AA Mutation	p.Ser878Tyr(p.S878Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75836427:75836427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2665C>T
AA Mutation	p.His889Tyr(p.H889Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75808054:75808054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190179934
CDS Mutation	c.1072C>T
AA Mutation	p.Arg358Cys(p.R358C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75841820:75841820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3169C>T
AA Mutation	p.Leu1057Phe(p.L1057F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75823655:75823655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370412695
CDS Mutation	c.2032G>A
AA Mutation	p.Ala678Thr(p.A678T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000465261
Start	75821608:75821608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774756205
CDS Mutation	c.1940C>T
AA Mutation	p.Thr647Met(p.T647M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75834351:75834351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2491C>T
AA Mutation	p.His831Tyr(p.H831Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75841122:75841122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2897G>A
AA Mutation	p.Arg966His(p.R966H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75808187:75808187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1205T>G
AA Mutation	p.Leu402Arg(p.L402R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75841155:75841155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2930G>T
AA Mutation	p.Arg977Met(p.R977M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75821380:75821380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760259550
CDS Mutation	c.1712G>A
AA Mutation	p.Arg571His(p.R571H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75834372:75834372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369234596
CDS Mutation	c.2512C>T
AA Mutation	p.Arg838Cys(p.R838C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75849202:75849202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3575G>T
AA Mutation	p.Arg1192Ile(p.R1192I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75807587:75807587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605G>T
AA Mutation	p.Arg202Met(p.R202M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75804391:75804391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375314137
CDS Mutation	c.65C>T
AA Mutation	p.Ala22Val(p.A22V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75807953:75807953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971T>G
AA Mutation	p.Phe324Cys(p.F324C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75819418:75819418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372334697
CDS Mutation	c.1391G>A
AA Mutation	p.Arg464Gln(p.R464Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75805619:75805619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356G>A
AA Mutation	p.Arg119His(p.R119H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75840097:75840097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766012567
CDS Mutation	c.2765C>T
AA Mutation	p.Ser922Leu(p.S922L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75853327:75853327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3901T>C
AA Mutation	p.Ser1301Pro(p.S1301P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75821258:75821258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1590A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75853143:75853143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3717G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75808092:75808092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75833146:75833146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2346C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000465261
Start	75807821:75807821(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.843delA
AA Mutation	p.Asp282MetfsTer3(p.D282Mfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000465261
Start	75849234:75849234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3607C>T
AA Mutation	p.Arg1203Ter(p.R1203*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000465261
Start	75841828:75841829(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.3187_3188dupAG
AA Mutation	p.Lys1064GlyfsTer36(p.K1064Gfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000465261
Start	75856609:75856609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4065+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LMO7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75821257:75821257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558204044
CDS Mutation	c.1589G>A
AA Mutation	p.Arg530Gln(p.R530Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75823592:75823592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1969G>A
AA Mutation	p.Asp657Asn(p.D657N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75834335:75834335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2475G>T
AA Mutation	p.Lys825Asn(p.K825N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75805587:75805587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.324A>G
AA Mutation	p.Ile108Met(p.I108M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75857958:75857958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376296039
CDS Mutation	c.4103C>T
AA Mutation	p.Thr1368Met(p.T1368M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000465261
Start	75835322:75835322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377551293
CDS Mutation	c.2617G>A
AA Mutation	p.Glu873Lys(p.E873K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000465261
Start	75853119:75853119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779068382
CDS Mutation	c.3693C>T
Mutation Classification	Silent
Feature Type	Transcript