Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NID1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236013444:236013444(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2371C>T
AA Mutation p.Pro791Ser(p.P791S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 235993815:235993815(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs144659138
CDS Mutation c.2585C>T
AA Mutation p.Ala862Val(p.A862V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236048858:236048858(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.357G>T
AA Mutation p.Lys119Asn(p.K119N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 235993696:235993696(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2704G>A
AA Mutation p.Asp902Asn(p.D902N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236045557:236045557(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200279383
CDS Mutation c.652G>A
AA Mutation p.Val218Met(p.V218M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236026111:236026111(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1769C>T
AA Mutation p.Thr590Met(p.T590M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000264187
Start 235978997:235978997(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3620A>G
AA Mutation p.Gln1207Arg(p.Q1207R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 235993842:235993842(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2558G>A
AA Mutation p.Arg853Gln(p.R853Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236048695:236048695(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.520G>T
AA Mutation p.Gly174Cys(p.G174C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236038229:236038229(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs16833154
CDS Mutation c.1160G>A
AA Mutation p.Arg387His(p.R387H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236024150:236024150(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146611286
CDS Mutation c.2048C>T
AA Mutation p.Ala683Val(p.A683V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 235981717:235981717(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3121A>G
AA Mutation p.Asn1041Asp(p.N1041D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236032536:236032536(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767968651
CDS Mutation c.1402C>T
AA Mutation p.Arg468Cys(p.R468C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236045463:236045463(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.746T>C
AA Mutation p.Leu249Ser(p.L249S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236024081:236024081(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759141799
CDS Mutation c.2117G>A
AA Mutation p.Arg706Gln(p.R706Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 235993746:235993746(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749480537
CDS Mutation c.2654C>T
AA Mutation p.Ala885Val(p.A885V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236045466:236045466(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.743A>G
AA Mutation p.Asn248Ser(p.N248S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 235979039:235979039(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3578C>T
AA Mutation p.Thr1193Ile(p.T1193I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236064865:236064865(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.215A>G
AA Mutation p.Asp72Gly(p.D72G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236026025:236026025(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148420954
CDS Mutation c.1855G>A
AA Mutation p.Val619Ile(p.V619I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 236038123:236038123(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1266C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 22
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 236011931:236011931(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775151010
CDS Mutation c.2517C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 235981694:235981694(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148662892
CDS Mutation c.3144G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 235979023:235979023(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3594C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 235977879:235977879(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772051661
CDS Mutation c.3732C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 236025936:236025936(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1944C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 235979065:235979065(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs546812606
CDS Mutation c.3552G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 236048786:236048786(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.429G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 236032594:236032594(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1344G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 236048801:236048801(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.414C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 236029596:236029596(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs368325718
CDS Mutation c.1692C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 235993664:235993664(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2736G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 236048762:236048762(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201727792
CDS Mutation c.453C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 235993868:235993868(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2532G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 235993847:235993847(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765999192
CDS Mutation c.2553C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 236042055:236042055(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.990C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 235993766:235993766(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2634C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence stop_gained
Transcription ID ENST00000264187
Start 236045475:236045475(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.734C>G
AA Mutation p.Ser245Ter(p.S245*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence splice_donor_variant
Transcription ID ENST00000264187
Start 236041909:236041909(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1135+1G>A
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> NID1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 235981626:235981626(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs533832624
CDS Mutation c.3212C>T
AA Mutation p.Thr1071Met(p.T1071M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 235993831:235993831(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2569C>A
AA Mutation p.Leu857Ile(p.L857I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236026052:236026052(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765678235
CDS Mutation c.1828C>T
AA Mutation p.Arg610Cys(p.R610C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000264187
Start 236012019:236012019(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375233632
CDS Mutation c.2429G>A
AA Mutation p.Arg810Gln(p.R810Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 236042211:236042211(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371831151
CDS Mutation c.834C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 236042043:236042043(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146353651
CDS Mutation c.1002G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 235993853:235993853(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2547C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 235977960:235977960(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373795201
CDS Mutation c.3651C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000264187
Start 235980593:235980593(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771149872
CDS Mutation c.3288C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000264187
Start 235977990:235977990(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3623-2A>C
Mutation Classification Splice_Site
Feature Type Transcript