Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDH12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	22078637:22078637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.40C>A
AA Mutation	p.Leu14Met(p.L14M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21760619:21760619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1572C>A
AA Mutation	p.Phe524Leu(p.F524L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21755720:21755720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1756A>C
AA Mutation	p.Thr586Pro(p.T586P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21783393:21783393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143124599
CDS Mutation	c.1358C>T
AA Mutation	p.Ala453Val(p.A453V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21802303:21802303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1120A>G
AA Mutation	p.Ser374Gly(p.S374G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21854722:21854722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371189490
CDS Mutation	c.595G>A
AA Mutation	p.Val199Ile(p.V199I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21783427:21783427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551198422
CDS Mutation	c.1324G>A
AA Mutation	p.Ala442Thr(p.A442T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21751880:21751880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2242G>A
AA Mutation	p.Ala748Thr(p.A748T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21783369:21783369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382C>T
AA Mutation	p.Ala461Val(p.A461V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	22078525:22078525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.152G>A
AA Mutation	p.Arg51His(p.R51H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21842212:21842212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.763G>T
AA Mutation	p.Val255Phe(p.V255F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21817078:21817078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.869G>T
AA Mutation	p.Arg290Ile(p.R290I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21752153:21752153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1969G>A
AA Mutation	p.Val657Ile(p.V657I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21764988:21764988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1505A>C
AA Mutation	p.Lys502Thr(p.K502T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21752192:21752192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1930G>T
AA Mutation	p.Asp644Tyr(p.D644Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21755710:21755710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1766T>C
AA Mutation	p.Val589Ala(p.V589A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21765079:21765079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1414A>G
AA Mutation	p.Lys472Glu(p.K472E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382254
Start	21802292:21802292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1131C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382254
Start	21751842:21751842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2280A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382254
Start	21816990:21816990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382254
Start	21802220:21802220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1203C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382254
Start	22078476:22078476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382254
Start	21802271:21802271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382254
Start	21751791:21751791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2331C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382254
Start	21802301:21802301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1122C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382254
Start	21752229:21752229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1893T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382254
Start	21842282:21842282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.693A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382254
Start	21854777:21854777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.540C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000382254
Start	21783439:21783439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1312G>T
AA Mutation	p.Glu438Ter(p.E438*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000382254
Start	21817040:21817040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907G>T
AA Mutation	p.Glu303Ter(p.E303*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000382254
Start	21842293:21842293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682G>T
AA Mutation	p.Glu228Ter(p.E228*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382254
Start	21854747:21854748(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.569dupC
AA Mutation	p.Thr191AspfsTer22(p.T191Dfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000382254
Start	21783496:21783496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1257-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CDH12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	22078634:22078634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43T>C
AA Mutation	p.Phe15Leu(p.F15L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21802210:21802210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1213G>A
AA Mutation	p.Ala405Thr(p.A405T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21760587:21760587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1604A>C
AA Mutation	p.Lys535Thr(p.K535T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21975235:21975235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765635488
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Cys(p.R128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21751836:21751836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2286C>A
AA Mutation	p.Asp762Glu(p.D762E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21817031:21817031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750157329
CDS Mutation	c.916T>C
AA Mutation	p.Tyr306His(p.Y306H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21842272:21842272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.703G>T
AA Mutation	p.Val235Leu(p.V235L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	21854719:21854719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.598T>A
AA Mutation	p.Tyr200Asn(p.Y200N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000382254
Start	22078588:22078588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89C>G
AA Mutation	p.Thr30Ser(p.T30S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000382254
Start	22078496:22078497(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.180_181insC
AA Mutation	p.Phe61LeufsTer45(p.F61Lfs*45)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript