Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DLEC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38117978:38117978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780941716
CDS Mutation	c.4658C>T
AA Mutation	p.Ala1553Val(p.A1553V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38114358:38114358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202226243
CDS Mutation	c.3683C>T
AA Mutation	p.Pro1228Leu(p.P1228L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38117558:38117558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4432A>G
AA Mutation	p.Met1478Val(p.M1478V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38062274:38062274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779T>G
AA Mutation	p.Leu260Arg(p.L260R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38100298:38100298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2737G>A
AA Mutation	p.Asp913Asn(p.D913N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38059834:38059834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655T>C
AA Mutation	p.Phe219Leu(p.F219L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38115030:38115030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752782524
CDS Mutation	c.3833G>A
AA Mutation	p.Arg1278His(p.R1278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38095061:38095061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2102C>A
AA Mutation	p.Ser701Tyr(p.S701Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38086247:38086247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752369082
CDS Mutation	c.1442C>T
AA Mutation	p.Pro481Leu(p.P481L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38039310:38039310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85C>T
AA Mutation	p.Pro29Ser(p.P29S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38117242:38117242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4340T>C
AA Mutation	p.Leu1447Pro(p.L1447P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38120590:38120590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4847A>G
AA Mutation	p.Tyr1616Cys(p.Y1616C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38115021:38115021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200604389
CDS Mutation	c.3824G>A
AA Mutation	p.Arg1275Gln(p.R1275Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38107721:38107721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3002A>G
AA Mutation	p.Gln1001Arg(p.Q1001R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38059792:38059792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613C>A
AA Mutation	p.His205Asn(p.H205N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38097792:38097792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370165845
CDS Mutation	c.2614C>T
AA Mutation	p.Arg872Cys(p.R872C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38039592:38039592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775199798
CDS Mutation	c.367A>G
AA Mutation	p.Ser123Gly(p.S123G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38039430:38039430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.205C>T
AA Mutation	p.Leu69Phe(p.L69F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000308059
Start	38120518:38120518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4775C>A
AA Mutation	p.Pro1592His(p.P1592H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38039300:38039300(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38039460:38039460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.235C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38112316:38112316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3621C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38039627:38039627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.402G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38084223:38084223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1239G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38110117:38110117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3279C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38092855:38092855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1731C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38062284:38062284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755377750
CDS Mutation	c.789C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38062182:38062182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38093696:38093696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1848G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308059
Start	38100410:38100410(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2852delA
AA Mutation	p.Asn951MetfsTer67(p.N951Mfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308059
Start	38116521:38116521(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3928delT
AA Mutation	p.Tyr1310MetfsTer121(p.Y1310Mfs*121)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	stop_gained
Transcription ID	ENST00000308059
Start	38086359:38086359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1554G>A
AA Mutation	p.Trp518Ter(p.W518*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	stop_gained
Transcription ID	ENST00000308059
Start	38062773:38062773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1066G>T
AA Mutation	p.Glu356Ter(p.E356*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308059
Start	38062699:38062700(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs773357781
CDS Mutation	c.999dupT
AA Mutation	p.Pro334SerfsTer3(p.P334Sfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308059
Start	38085431:38085432(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs756971918
CDS Mutation	c.1425dupC
AA Mutation	p.Val476ArgfsTer58(p.V476Rfs*58)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DLEC1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38092840:38092840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1716C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38062284:38062284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755377750
CDS Mutation	c.789C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308059
Start	38084223:38084223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1239G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308059
Start	38120547:38120548(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs780359904
CDS Mutation	c.4815_4816dupGA
AA Mutation	p.Met1606ArgfsTer45(p.M1606Rfs*45)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000308059
Start	38121783:38121783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5020+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript