Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNXB

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32067823:32067823(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6382C>A
AA Mutation p.Gln2128Lys(p.Q2128K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32072060:32072060(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4920G>T
AA Mutation p.Lys1640Asn(p.K1640N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32095773:32095773(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2080C>A
AA Mutation p.Pro694Thr(p.P694T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32061544:32061544(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7345G>A
AA Mutation p.Asp2449Asn(p.D2449N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32068441:32068441(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756050937
CDS Mutation c.6169G>A
AA Mutation p.Gly2057Ser(p.G2057S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000451343
Start 32043823:32043823(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745733950
CDS Mutation c.743C>T
AA Mutation p.Ala248Val(p.A248V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32068399:32068399(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs200319996
CDS Mutation c.6211G>A
AA Mutation p.Gly2071Arg(p.G2071R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32088841:32088841(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2723T>A
AA Mutation p.Val908Asp(p.V908D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000375244
Start 32089047:32089047(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2517G>A
AA Mutation p.Met839Ile(p.M839I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32096298:32096298(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1555A>C
AA Mutation p.Thr519Pro(p.T519P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32056038:32056038(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8280G>T
AA Mutation p.Gln2760His(p.Q2760H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32069645:32069645(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768187269
CDS Mutation c.5495C>T
AA Mutation p.Pro1832Leu(p.P1832L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32062346:32062346(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764604500
CDS Mutation c.6979G>A
AA Mutation p.Glu2327Lys(p.E2327K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32056717:32056717(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201037895
CDS Mutation c.8012C>T
AA Mutation p.Ala2671Val(p.A2671V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32070136:32070136(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747658329
CDS Mutation c.5269G>A
AA Mutation p.Gly1757Ser(p.G1757S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32068644:32068644(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754160588
CDS Mutation c.5966G>A
AA Mutation p.Arg1989His(p.R1989H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32062394:32062394(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777077674
CDS Mutation c.6931G>A
AA Mutation p.Val2311Met(p.V2311M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32068704:32068704(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773297077
CDS Mutation c.5906C>T
AA Mutation p.Pro1969Leu(p.P1969L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000451343
Start 32044395:32044395(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.536G>A
AA Mutation p.Arg179His(p.R179H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000451343
Start 32045174:32045174(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs560288296
CDS Mutation c.46G>A
AA Mutation p.Val16Met(p.V16M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32096789:32096789(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1064G>A
AA Mutation p.Gly355Asp(p.G355D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32065076:32065076(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs747302691
CDS Mutation c.6586C>T
AA Mutation p.Arg2196Cys(p.R2196C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32067838:32067838(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201764050
CDS Mutation c.6367G>A
AA Mutation p.Asp2123Asn(p.D2123N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32096894:32096894(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.959G>A
AA Mutation p.Arg320His(p.R320H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32069810:32069810(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767799073
CDS Mutation c.5330G>A
AA Mutation p.Arg1777His(p.R1777H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32052795:32052795(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs41270454
CDS Mutation c.8990G>A
AA Mutation p.Arg2997His(p.R2997H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32065010:32065010(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs530280191
CDS Mutation c.6652G>A
AA Mutation p.Glu2218Lys(p.E2218K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32086055:32086055(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2843C>T
AA Mutation p.Thr948Met(p.T948M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32095853:32095853(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2000G>A
AA Mutation p.Cys667Tyr(p.C667Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32088829:32088829(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374779610
CDS Mutation c.2735G>A
AA Mutation p.Arg912Gln(p.R912Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000451343
Start 32045135:32045135(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.85T>G
AA Mutation p.Leu29Val(p.L29V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32064990:32064990(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6672C>A
AA Mutation p.Phe2224Leu(p.F2224L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000451343
Start 32042126:32042126(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1642C>T
AA Mutation p.Arg548Cys(p.R548C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32061664:32061664(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7225C>G
AA Mutation p.Pro2409Ala(p.P2409A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32067678:32067678(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6527C>A
AA Mutation p.Ser2176Tyr(p.S2176Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32052700:32052700(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs543265032
CDS Mutation c.9085G>A
AA Mutation p.Val3029Met(p.V3029M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32056601:32056601(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8128G>T
AA Mutation p.Val2710Phe(p.V2710F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32056691:32056691(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759066378
CDS Mutation c.8038G>A
AA Mutation p.Gly2680Arg(p.G2680R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32056844:32056844(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7885C>G
AA Mutation p.Pro2629Ala(p.P2629A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32053597:32053597(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8582G>A
AA Mutation p.Ser2861Asn(p.S2861N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32088980:32088980(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs570806090
CDS Mutation c.2584C>T
AA Mutation p.Arg862Cys(p.R862C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32085896:32085896(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768607753
CDS Mutation c.3002C>T
AA Mutation p.Pro1001Leu(p.P1001L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 43
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32053525:32053525(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8654C>T
AA Mutation p.Pro2885Leu(p.P2885L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32053695:32053695(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367949241
CDS Mutation c.8484A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32097148:32097148(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.705C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32096239:32096239(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1614C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32052974:32052974(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8811C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32056617:32056617(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753413229
CDS Mutation c.8112C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000451343
Start 32042518:32042518(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs745360751
CDS Mutation c.1434C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32084558:32084558(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749807972
CDS Mutation c.3300C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000451343
Start 32042575:32042575(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755633941
CDS Mutation c.1377C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000451343
Start 32041801:32041801(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1890C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32058371:32058371(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7512C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32053467:32053467(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.8712A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32052707:32052707(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.9078G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000451343
Start 32042557:32042557(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766412096
CDS Mutation c.1395C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000451343
Start 32042485:32042485(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1467C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 58
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32085952:32085952(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369219469
CDS Mutation c.2946C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 59
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32096020:32096020(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767856741
CDS Mutation c.1833C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 60
Mutation Consequence synonymous_variant
Transcription ID ENST00000451343
Start 32045175:32045175(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746778977
CDS Mutation c.45C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 61
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32085895:32085895(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756574808
CDS Mutation c.3003G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 62
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32067839:32067839(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753403637
CDS Mutation c.6366C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 63
Mutation Consequence frameshift_variant
Transcription ID ENST00000375244
Start 32056832:32056832(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.7897delG
AA Mutation p.Glu2633SerfsTer2(p.E2633Sfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 64
Mutation Consequence frameshift_variant
Transcription ID ENST00000375244
Start 32067907:32067907(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.6298delG
AA Mutation p.Glu2100SerfsTer2(p.E2100Sfs*2)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 65
Mutation Consequence frameshift_variant
Transcription ID ENST00000375244
Start 32096912:32096912(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.941delG
AA Mutation p.Gly314AlafsTer257(p.G314Afs*257)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 66
Mutation Consequence frameshift_variant
Transcription ID ENST00000375244
Start 32067750:32067750(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.6455delG
AA Mutation p.Gly2152AlafsTer46(p.G2152Afs*46)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 67
Mutation Consequence stop_gained
Transcription ID ENST00000451343
Start 32042316:32042316(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1544G>A
AA Mutation p.Trp515Ter(p.W515*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 68
Mutation Consequence stop_gained
Transcription ID ENST00000375244
Start 32068942:32068942(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5782G>T
AA Mutation p.Gly1928Ter(p.G1928*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 69
Mutation Consequence stop_gained
Transcription ID ENST00000375244
Start 32062314:32062314(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7011C>A
AA Mutation p.Tyr2337Ter(p.Y2337*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 70
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000375244
Start 32058058:32058058(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7825G>T
AA Mutation p.Glu2609Ter(p.E2609*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> TNXB

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32061715:32061715(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs56144119
CDS Mutation c.7174G>A
AA Mutation p.Glu2392Lys(p.E2392K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32062466:32062466(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6859G>A
AA Mutation p.Glu2287Lys(p.E2287K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000451343
Start 32043856:32043856(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376486710
CDS Mutation c.710G>A
AA Mutation p.Arg237Gln(p.R237Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000375244
Start 32069642:32069642(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5498G>C
AA Mutation p.Gly1833Ala(p.G1833A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32070206:32070206(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs556400560
CDS Mutation c.5199C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32088885:32088885(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2679G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000375244
Start 32067713:32067713(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6492C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000451343
Start 32045100:32045100(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.120C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000451343
Start 32045175:32045175(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs746778977
CDS Mutation c.45C>T
Mutation Classification Silent
Feature Type Transcript