Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LIFR

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38481815:38481815(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3074C>A
AA Mutation p.Thr1025Asn(p.T1025N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38510500:38510500(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749557070
CDS Mutation c.955G>A
AA Mutation p.Glu319Lys(p.E319K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38481936:38481936(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2953G>A
AA Mutation p.Ala985Thr(p.A985T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38485866:38485866(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2450G>A
AA Mutation p.Gly817Asp(p.G817D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38530595:38530595(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.53A>C
AA Mutation p.Lys18Thr(p.K18T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38499533:38499533(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1651A>C
AA Mutation p.Asn551His(p.N551H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38504080:38504080(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1333A>C
AA Mutation p.Asn445His(p.N445H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38481803:38481803(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3086G>A
AA Mutation p.Arg1029Lys(p.R1029K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38506578:38506578(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1046T>G
AA Mutation p.Ile349Ser(p.I349S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38506048:38506048(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1148A>G
AA Mutation p.Lys383Arg(p.K383R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38490220:38490220(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776173910
CDS Mutation c.2137C>T
AA Mutation p.Arg713Cys(p.R713C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38528787:38528787(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.196T>C
AA Mutation p.Ser66Pro(p.S66P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38530632:38530632(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373771721
CDS Mutation c.16G>A
AA Mutation p.Val6Ile(p.V6I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38484802:38484802(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2564G>T
AA Mutation p.Ser855Ile(p.S855I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38502709:38502709(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1528C>T
AA Mutation p.Arg510Cys(p.R510C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38482083:38482083(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746053471
CDS Mutation c.2806C>T
AA Mutation p.Arg936Cys(p.R936C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38485900:38485900(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2416A>C
AA Mutation p.Ser806Arg(p.S806R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38502662:38502662(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1575A>C
AA Mutation p.Lys525Asn(p.K525N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38502715:38502715(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769058491
CDS Mutation c.1522C>T
AA Mutation p.Arg508Trp(p.R508W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38523448:38523448(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757892555
CDS Mutation c.532C>T
AA Mutation p.Arg178Cys(p.R178C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000263409
Start 38502639:38502639(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1598C>A
AA Mutation p.Ala533Asp(p.A533D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38484841:38484841(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2525T>A
AA Mutation p.Ile842Asn(p.I842N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38506025:38506025(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373421600
CDS Mutation c.1171G>A
AA Mutation p.Glu391Lys(p.E391K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38510473:38510473(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.982T>G
AA Mutation p.Phe328Val(p.F328V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38527252:38527252(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.300T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38481709:38481709(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762094729
CDS Mutation c.3180A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38493679:38493679(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142392717
CDS Mutation c.1992G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38496437:38496437(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1830A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38484861:38484861(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747783999
CDS Mutation c.2505A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38496590:38496590(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1677A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38484840:38484840(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2526C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence frameshift_variant
Transcription ID ENST00000263409
Start 38490258:38490258(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2099delT
AA Mutation p.Phe700SerfsTer16(p.F700Sfs*16)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 33
Mutation Consequence stop_gained
Transcription ID ENST00000263409
Start 38496478:38496478(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs121912501
CDS Mutation c.1789C>T
AA Mutation p.Arg597Ter(p.R597*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence stop_gained
Transcription ID ENST00000263409
Start 38493612:38493612(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2059G>T
AA Mutation p.Glu687Ter(p.E687*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence stop_gained
Transcription ID ENST00000263409
Start 38490199:38490199(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2158G>T
AA Mutation p.Glu720Ter(p.E720*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> LIFR

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38504070:38504070(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1343C>A
AA Mutation p.Ala448Asp(p.A448D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38484781:38484781(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2585G>A
AA Mutation p.Arg862Gln(p.R862Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38490219:38490219(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2138G>T
AA Mutation p.Arg713Leu(p.R713L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38493774:38493774(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1897A>G
AA Mutation p.Ile633Val(p.I633V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38481758:38481758(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3131C>A
AA Mutation p.Ser1044Tyr(p.S1044Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38510500:38510500(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749557070
CDS Mutation c.955G>A
AA Mutation p.Glu319Lys(p.E319K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000263409
Start 38496420:38496420(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1847C>T
AA Mutation p.Ser616Leu(p.S616L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38482162:38482162(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2727G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38493679:38493679(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142392717
CDS Mutation c.1992G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38485835:38485835(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2481G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000263409
Start 38489229:38489229(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2184A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000263409
Start 38481693:38481693(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3196C>T
AA Mutation p.Arg1066Ter(p.R1066*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000263409
Start 38482630:38482630(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2629G>T
AA Mutation p.Glu877Ter(p.E877*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript