Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDH4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61895000:61895000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1141A>G
AA Mutation	p.Thr381Ala(p.T381A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61844701:61844701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751431226
CDS Mutation	c.610C>T
AA Mutation	p.Arg204Trp(p.R204W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61923476:61923476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1400C>A
AA Mutation	p.Ala467Asp(p.A467D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61773166:61773166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.560C>T
AA Mutation	p.Pro187Leu(p.P187L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61928213:61928213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777402708
CDS Mutation	c.1795G>A
AA Mutation	p.Gly599Arg(p.G599R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61773067:61773067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370608791
CDS Mutation	c.461C>T
AA Mutation	p.Pro154Leu(p.P154L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61910482:61910482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249G>A
AA Mutation	p.Asp417Asn(p.D417N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61743761:61743761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757506706
CDS Mutation	c.368A>G
AA Mutation	p.Gln123Arg(p.Q123R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61773154:61773154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.548G>A
AA Mutation	p.Arg183His(p.R183H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61873881:61873881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1031C>T
AA Mutation	p.Ala344Val(p.A344V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61743719:61743719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.326C>T
AA Mutation	p.Thr109Ile(p.T109I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61844702:61844702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611G>A
AA Mutation	p.Arg204Gln(p.R204Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61910465:61910465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1232C>A
AA Mutation	p.Ala411Glu(p.A411E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61873731:61873731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881C>T
AA Mutation	p.Thr294Ile(p.T294I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61923509:61923509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1433C>T
AA Mutation	p.Ala478Val(p.A478V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61844773:61844773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757336738
CDS Mutation	c.682C>T
AA Mutation	p.Arg228Trp(p.R228W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61929633:61929633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200733156
CDS Mutation	c.2030G>A
AA Mutation	p.Arg677His(p.R677H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61933071:61933071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142330895
CDS Mutation	c.2326G>A
AA Mutation	p.Val776Ile(p.V776I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61910516:61910516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283C>T
AA Mutation	p.Ala428Val(p.A428V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61928415:61928415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1997G>A
AA Mutation	p.Arg666His(p.R666H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61773143:61773143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.537C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61928365:61928365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751297571
CDS Mutation	c.1947C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61934121:61934121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762550906
CDS Mutation	c.2445C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61743651:61743651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142221912
CDS Mutation	c.258C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61923630:61923630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1554G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61873783:61873783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.933C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61873804:61873804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.954C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61743690:61743690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs79132902
CDS Mutation	c.297G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61895038:61895038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369270154
CDS Mutation	c.1179C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000614565
Start	61936770:61936770(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2583delC
AA Mutation	p.Tyr862MetfsTer22(p.Y862Mfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000614565
Start	61936888:61936888(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2700delG
AA Mutation	p.Arg902AspfsTer17(p.R902Dfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000614565
Start	61923636:61923637(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs764543058
CDS Mutation	c.1566dupC
AA Mutation	p.Gly523ArgfsTer13(p.G523Rfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CDH4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61910524:61910524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1291C>T
AA Mutation	p.Arg431Cys(p.R431C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61910458:61910458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557605363
CDS Mutation	c.1225G>A
AA Mutation	p.Val409Met(p.V409M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61936746:61936746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373341715
CDS Mutation	c.2554G>A
AA Mutation	p.Ala852Thr(p.A852T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61894922:61894922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1063T>G
AA Mutation	p.Tyr355Asp(p.Y355D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61929675:61929675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2072T>G
AA Mutation	p.Ile691Ser(p.I691S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000614565
Start	61743746:61743746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373320390
CDS Mutation	c.353G>A
AA Mutation	p.Arg118Gln(p.R118Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61929652:61929652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201703403
CDS Mutation	c.2049C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61773086:61773086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149210026
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000614565
Start	61928287:61928287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753159244
CDS Mutation	c.1869C>T
Mutation Classification	Silent
Feature Type	Transcript