Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDH11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64950797:64950797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1864G>A
AA Mutation	p.Ala622Thr(p.A622T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000268603
Start	64971579:64971579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1642G>T
AA Mutation	p.Asp548Tyr(p.D548Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64972047:64972047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1408G>A
AA Mutation	p.Ala470Thr(p.A470T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	65004690:65004690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180C>A
AA Mutation	p.Phe60Leu(p.F60L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	65004755:65004755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.115C>T
AA Mutation	p.His39Tyr(p.H39Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64948063:64948063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1931A>G
AA Mutation	p.Lys644Arg(p.K644R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64948071:64948071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1923A>C
AA Mutation	p.Arg641Ser(p.R641S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	65004842:65004842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377191094
CDS Mutation	c.28G>A
AA Mutation	p.Ala10Thr(p.A10T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64951004:64951004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776736292
CDS Mutation	c.1657G>A
AA Mutation	p.Val553Met(p.V553M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64971677:64971677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1544C>T
AA Mutation	p.Ala515Val(p.A515V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64971665:64971665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1556A>G
AA Mutation	p.Asp519Gly(p.D519G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64947662:64947662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2332C>A
AA Mutation	p.Arg778Ser(p.R778S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64947739:64947739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2255C>T
AA Mutation	p.Ala752Val(p.A752V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64972002:64972002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1453G>A
AA Mutation	p.Ala485Thr(p.A485T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64971582:64971582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1639C>G
AA Mutation	p.Arg547Gly(p.R547G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64998732:64998732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.353G>A
AA Mutation	p.Arg118Gln(p.R118Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64998588:64998588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497C>T
AA Mutation	p.Ala166Val(p.A166V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64998831:64998831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.254A>G
AA Mutation	p.Asp85Gly(p.D85G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64992975:64992975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.583G>A
AA Mutation	p.Ala195Thr(p.A195T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64998690:64998690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.395A>G
AA Mutation	p.Asp132Gly(p.D132G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64950829:64950829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1832T>G
AA Mutation	p.Leu611Arg(p.L611R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	65004736:65004736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.134G>T
AA Mutation	p.Gly45Val(p.G45V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64998611:64998611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.474G>T
AA Mutation	p.Glu158Asp(p.E158D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64988312:64988312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367827121
CDS Mutation	c.844G>A
AA Mutation	p.Val282Ile(p.V282I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64971658:64971658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1563G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64950999:64950999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200486624
CDS Mutation	c.1662C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64982200:64982200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1101T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64947924:64947924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2070T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64982101:64982101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs180715892
CDS Mutation	c.1200C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64950873:64950873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1788C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64982194:64982194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183737751
CDS Mutation	c.1107C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64973025:64973025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1269T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64982194:64982194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183737751
CDS Mutation	c.1107C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64982233:64982233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139053832
CDS Mutation	c.1068G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64950867:64950867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563299959
CDS Mutation	c.1794C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64998569:64998569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.516C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64998710:64998710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771186221
CDS Mutation	c.375G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64947861:64947861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200766127
CDS Mutation	c.2133G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268603
Start	64971643:64971644(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1577_1578insCC
AA Mutation	p.Arg526SerfsTer48(p.R526Sfs*48)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000268603
Start	64971644:64971645(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1576_1577insAC
AA Mutation	p.Arg526AsnfsTer48(p.R526Nfs*48)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CDH11

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000268603
Start	64971581:64971581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373610980
CDS Mutation	c.1640G>A
AA Mutation	p.Arg547Gln(p.R547Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000268603
Start	64973026:64973026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202032642
CDS Mutation	c.1268G>A
AA Mutation	p.Arg423His(p.R423H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64947765:64947765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145843219
CDS Mutation	c.2229C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	65004837:65004837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.33G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64950921:64950921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759807372
CDS Mutation	c.1740G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64947612:64947612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377222713
CDS Mutation	c.2382C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64982245:64982245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1056G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000268603
Start	64947861:64947861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200766127
CDS Mutation	c.2133G>A
Mutation Classification	Silent
Feature Type	Transcript