Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLIT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97001276:97001276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746275774
CDS Mutation	c.4441C>T
AA Mutation	p.Arg1481Cys(p.R1481C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97047024:97047024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1676G>A
AA Mutation	p.Gly559Glu(p.G559E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97066076:97066076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424G>A
AA Mutation	p.Glu142Lys(p.E142K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97004738:97004738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780115071
CDS Mutation	c.3665G>A
AA Mutation	p.Arg1222His(p.R1222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97006500:97006500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3562G>A
AA Mutation	p.Ala1188Thr(p.A1188T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97047714:97047714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1610G>A
AA Mutation	p.Arg537His(p.R537H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97042928:97042928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2137G>A
AA Mutation	p.Ala713Thr(p.A713T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97040094:97040094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372733842
CDS Mutation	c.2191C>T
AA Mutation	p.Arg731Cys(p.R731C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97046731:97046731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1776C>A
AA Mutation	p.Ser592Arg(p.S592R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97002894:97002894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3964G>A
AA Mutation	p.Glu1322Lys(p.E1322K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97006646:97006646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3416G>T
AA Mutation	p.Gly1139Val(p.G1139V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97063590:97063590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770874711
CDS Mutation	c.658G>A
AA Mutation	p.Asp220Asn(p.D220N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97047741:97047741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1583G>T
AA Mutation	p.Ser528Ile(p.S528I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97049042:97049042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773757484
CDS Mutation	c.1378G>A
AA Mutation	p.Glu460Lys(p.E460K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97011072:97011072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3262A>G
AA Mutation	p.Arg1088Gly(p.R1088G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97006503:97006503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546232285
CDS Mutation	c.3559C>T
AA Mutation	p.Arg1187Trp(p.R1187W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97031612:97031612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2504G>A
AA Mutation	p.Arg835His(p.R835H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97001275:97001275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148906362
CDS Mutation	c.4442G>A
AA Mutation	p.Arg1481His(p.R1481H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97056361:97056361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374390660
CDS Mutation	c.1261G>A
AA Mutation	p.Ala421Thr(p.A421T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97006572:97006572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3490A>G
AA Mutation	p.Lys1164Glu(p.K1164E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97031613:97031613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140889847
CDS Mutation	c.2503C>T
AA Mutation	p.Arg835Cys(p.R835C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97060144:97060144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956A>G
AA Mutation	p.Asn319Ser(p.N319S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97057237:97057237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130T>G
AA Mutation	p.Phe377Cys(p.F377C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97034516:97034516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2393C>T
AA Mutation	p.Ser798Phe(p.S798F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97066030:97066030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537899049
CDS Mutation	c.470C>T
AA Mutation	p.Thr157Met(p.T157M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97042963:97042963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2102C>A
AA Mutation	p.Pro701His(p.P701H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97040093:97040093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2192G>A
AA Mutation	p.Arg731His(p.R731H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97004089:97004089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774613268
CDS Mutation	c.3844G>A
AA Mutation	p.Glu1282Lys(p.E1282K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97004098:97004098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3835C>A
AA Mutation	p.Leu1279Ile(p.L1279I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97043396:97043396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772987008
CDS Mutation	c.1971C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97043471:97043471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143659636
CDS Mutation	c.1896C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97031662:97031662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2454T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97004084:97004084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749650797
CDS Mutation	c.3849G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97063519:97063519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752336314
CDS Mutation	c.729G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97002940:97002940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148583876
CDS Mutation	c.3918C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97019004:97019004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190883090
CDS Mutation	c.2850C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97002841:97002841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777541136
CDS Mutation	c.4017C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97014074:97014074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369250356
CDS Mutation	c.3054C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266058
Start	97001333:97001333(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.4384delG
AA Mutation	p.Asp1462ThrfsTer42(p.D1462Tfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLIT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97002173:97002173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267602656
CDS Mutation	c.4351G>A
AA Mutation	p.Glu1451Lys(p.E1451K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97047771:97047771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373698645
CDS Mutation	c.1553G>A
AA Mutation	p.Arg518His(p.R518H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97013771:97013771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371409196
CDS Mutation	c.3173C>T
AA Mutation	p.Ala1058Val(p.A1058V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000266058
Start	97030824:97030824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2515C>A
AA Mutation	p.Leu839Ile(p.L839I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266058
Start	97046752:97046752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565102855
CDS Mutation	c.1755C>T
Mutation Classification	Silent
Feature Type	Transcript