Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLIT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168671222:168671222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4103C>T
AA Mutation	p.Ala1368Val(p.A1368V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000519560
Start	169193549:169193549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766150043
CDS Mutation	c.343C>T
AA Mutation	p.Arg115Cys(p.R115C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168671387:168671387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3938A>G
AA Mutation	p.Asn1313Ser(p.N1313S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000519560
Start	168760863:168760863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1684A>T
AA Mutation	p.Ile562Leu(p.I562L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168753888:168753888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374334394
CDS Mutation	c.1805G>A
AA Mutation	p.Arg602His(p.R602H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168710946:168710946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2668A>G
AA Mutation	p.Met890Val(p.M890V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000519560
Start	168795577:168795577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143425660
CDS Mutation	c.937C>T
AA Mutation	p.Arg313Cys(p.R313C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168724422:168724422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144594798
CDS Mutation	c.2333C>T
AA Mutation	p.Thr778Met(p.T778M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168762621:168762621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1528C>T
AA Mutation	p.Arg510Cys(p.R510C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168684050:168684050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3602A>G
AA Mutation	p.Asn1201Ser(p.N1201S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168844600:168844600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779381240
CDS Mutation	c.541C>T
AA Mutation	p.Arg181Cys(p.R181C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168823285:168823285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.604A>G
AA Mutation	p.Asn202Asp(p.N202D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000519560
Start	168817462:168817462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631C>A
AA Mutation	p.Arg211Ser(p.R211S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168823271:168823271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618G>T
AA Mutation	p.Lys206Asn(p.K206N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168789608:168789608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759032960
CDS Mutation	c.1031C>T
AA Mutation	p.Ser344Leu(p.S344L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168666478:168666478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4548G>C
AA Mutation	p.Glu1516Asp(p.E1516D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168753889:168753889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577365804
CDS Mutation	c.1804C>T
AA Mutation	p.Arg602Cys(p.R602C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000519560
Start	168844584:168844584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.557T>C
AA Mutation	p.Leu186Pro(p.L186P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168774259:168774259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1271C>T
AA Mutation	p.Ala424Val(p.A424V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	169251451:169251451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206A>T
AA Mutation	p.Asp69Val(p.D69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168685755:168685755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748887345
CDS Mutation	c.3487G>A
AA Mutation	p.Val1163Met(p.V1163M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168883279:168883279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769505903
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168696341:168696341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61746224
CDS Mutation	c.3033C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168795548:168795548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168687026:168687026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3267C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168696320:168696320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766410120
CDS Mutation	c.3054C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168772830:168772830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267600543
CDS Mutation	c.1410C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	169193496:169193496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771277109
CDS Mutation	c.396G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168785915:168785915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1143A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168685795:168685795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3447C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168669829:168669829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4290C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168883303:168883303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144526633
CDS Mutation	c.447G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168772869:168772869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762828706
CDS Mutation	c.1371C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168685756:168685756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148625020
CDS Mutation	c.3486C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168823298:168823298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.591G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168696329:168696329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3045C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168684007:168684007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3645G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168692690:168692690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775114129
CDS Mutation	c.3093C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168772860:168772860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771710067
CDS Mutation	c.1380C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168753896:168753896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559665628
CDS Mutation	c.1797C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168806526:168806526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367972639
CDS Mutation	c.855G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000519560
Start	168685904:168685904(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3338delC
AA Mutation	p.Pro1113HisfsTer108(p.P1113Hfs*108)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	stop_gained
Transcription ID	ENST00000519560
Start	168795511:168795511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767508476
CDS Mutation	c.1003C>T
AA Mutation	p.Arg335Ter(p.R335*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	44
Mutation Consequence	stop_gained
Transcription ID	ENST00000519560
Start	168748363:168748363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2209C>T
AA Mutation	p.Arg737Ter(p.R737*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLIT3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000519560
Start	169193549:169193549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766150043
CDS Mutation	c.343C>T
AA Mutation	p.Arg115Cys(p.R115C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168753039:168753039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768736861
CDS Mutation	c.1889C>T
AA Mutation	p.Ser630Leu(p.S630L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000519560
Start	168685756:168685756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3486C>A
AA Mutation	p.Phe1162Leu(p.F1162L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168710971:168710971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758437974
CDS Mutation	c.2643C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168753962:168753962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754934688
CDS Mutation	c.1731C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000519560
Start	168806547:168806547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834C>A
Mutation Classification	Silent
Feature Type	Transcript