Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FASN

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82091056:82091056(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1506G>T
AA Mutation p.Gln502His(p.Q502H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000306749
Start 82085035:82085035(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4409G>T
AA Mutation p.Arg1470Leu(p.R1470L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82083541:82083541(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5317G>A
AA Mutation p.Asp1773Asn(p.D1773N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82085369:82085369(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4156C>A
AA Mutation p.Leu1386Met(p.L1386M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82091564:82091564(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs762823912
CDS Mutation c.1150C>T
AA Mutation p.Arg384Cys(p.R384C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82085688:82085688(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751832838
CDS Mutation c.3916G>A
AA Mutation p.Ala1306Thr(p.A1306T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82084647:82084647(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs41283363
CDS Mutation c.4634G>A
AA Mutation p.Arg1545His(p.R1545H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82089312:82089312(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2038A>T
AA Mutation p.Met680Leu(p.M680L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82086547:82086547(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3439G>A
AA Mutation p.Ala1147Thr(p.A1147T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82091246:82091246(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs533081221
CDS Mutation c.1468C>T
AA Mutation p.Arg490Cys(p.R490C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82083312:82083312(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369955820
CDS Mutation c.5455C>T
AA Mutation p.Arg1819Trp(p.R1819W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82081206:82081206(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372065783
CDS Mutation c.6553C>T
AA Mutation p.Arg2185Trp(p.R2185W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82095358:82095358(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.242T>C
AA Mutation p.Leu81Pro(p.L81P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82087169:82087169(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3308C>T
AA Mutation p.Pro1103Leu(p.P1103L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82082658:82082658(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5788C>A
AA Mutation p.Arg1930Ser(p.R1930S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82091428:82091428(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1286G>A
AA Mutation p.Arg429His(p.R429H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82079376:82079376(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751413369
CDS Mutation c.7379C>T
AA Mutation p.Ala2460Val(p.A2460V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82085257:82085257(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748110849
CDS Mutation c.4268G>A
AA Mutation p.Arg1423His(p.R1423H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82091052:82091052(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758221850
CDS Mutation c.1510C>T
AA Mutation p.Arg504Cys(p.R504C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82092755:82092755(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs377076774
CDS Mutation c.836C>T
AA Mutation p.Ser279Leu(p.S279L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82083523:82083523(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5335C>T
AA Mutation p.Pro1779Ser(p.P1779S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82090380:82090380(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1865C>T
AA Mutation p.Ala622Val(p.A622V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82082637:82082637(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs17848945
CDS Mutation c.5809G>A
AA Mutation p.Val1937Ile(p.V1937I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82092465:82092465(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1019C>T
AA Mutation p.Ala340Val(p.A340V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82089672:82089672(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1925G>A
AA Mutation p.Cys642Tyr(p.C642Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000306749
Start 82081164:82081164(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747906170
CDS Mutation c.6595G>A
AA Mutation p.Glu2199Lys(p.E2199K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82082920:82082920(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142537824
CDS Mutation c.5761C>T
AA Mutation p.Arg1921Trp(p.R1921W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82082026:82082026(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373838349
CDS Mutation c.6146G>A
AA Mutation p.Arg2049Gln(p.R2049Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82088555:82088555(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2428G>A
AA Mutation p.Ala810Thr(p.A810T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82093625:82093625(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.427C>T
AA Mutation p.Arg143Trp(p.R143W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82084892:82084892(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4471G>T
AA Mutation p.Ala1491Ser(p.A1491S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82083595:82083595(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5263G>A
AA Mutation p.Ala1755Thr(p.A1755T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82082062:82082062(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6110C>T
AA Mutation p.Ala2037Val(p.A2037V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82084528:82084528(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4753C>A
AA Mutation p.Pro1585Thr(p.P1585T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82091049:82091049(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778595263
CDS Mutation c.1513G>A
AA Mutation p.Gly505Arg(p.G505R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000306749
Start 82088559:82088559(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2424C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000306749
Start 82090391:82090391(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1854C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000306749
Start 82088409:82088409(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2574A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000306749
Start 82086500:82086500(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781538664
CDS Mutation c.3486C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000306749
Start 82089271:82089271(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2079A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence synonymous_variant
Transcription ID ENST00000306749
Start 82091529:82091529(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770772130
CDS Mutation c.1185C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000306749
Start 82084601:82084601(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777624347
CDS Mutation c.4680C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence frameshift_variant
Transcription ID ENST00000306749
Start 82091478:82091478(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1236delC
AA Mutation p.Ala413HisfsTer39(p.A413Hfs*39)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 44
Mutation Consequence stop_gained
Transcription ID ENST00000306749
Start 82081197:82081197(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6562C>T
AA Mutation p.Gln2188Ter(p.Q2188*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence stop_gained
Transcription ID ENST00000306749
Start 82080695:82080695(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6823C>T
AA Mutation p.Arg2275Ter(p.R2275*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> FASN

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82087055:82087055(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3422G>T
AA Mutation p.Cys1141Phe(p.C1141F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82092544:82092544(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.940G>C
AA Mutation p.Ala314Pro(p.A314P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82095454:82095454(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201186614
CDS Mutation c.146G>A
AA Mutation p.Arg49Gln(p.R49Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000306749
Start 82081778:82081778(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs141935205
CDS Mutation c.6229G>A
AA Mutation p.Asp2077Asn(p.D2077N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000306749
Start 82086413:82086413(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758512736
CDS Mutation c.3573C>T
Mutation Classification Silent
Feature Type Transcript