Incidental Mutation 'IGL02456:Vps13c'
ID 294182
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vps13c
Ensembl Gene ENSMUSG00000035284
Gene Name vacuolar protein sorting 13C
Synonyms C230055H22Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02456
Quality Score
Status
Chromosome 9
Chromosomal Location 67747678-67902920 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 67860258 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 2825 (S2825P)
Ref Sequence ENSEMBL: ENSMUSP00000077040 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077879]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000077879
AA Change: S2825P

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000077040
Gene: ENSMUSG00000035284
AA Change: S2825P

DomainStartEndE-ValueType
Pfam:Chorein_N 3 117 1.3e-39 PFAM
low complexity region 151 165 N/A INTRINSIC
Pfam:VPS13 182 414 7.9e-70 PFAM
coiled coil region 422 443 N/A INTRINSIC
low complexity region 479 490 N/A INTRINSIC
Pfam:VPS13_mid_rpt 611 832 7.8e-71 PFAM
low complexity region 867 885 N/A INTRINSIC
low complexity region 1020 1036 N/A INTRINSIC
low complexity region 1112 1123 N/A INTRINSIC
Pfam:VPS13_mid_rpt 1172 1369 2.1e-14 PFAM
low complexity region 1552 1573 N/A INTRINSIC
Pfam:VPS13_mid_rpt 1685 1883 2.8e-13 PFAM
Blast:INB 2128 2403 2e-48 BLAST
Pfam:SHR-BD 2759 3013 9.9e-32 PFAM
Pfam:VPS13_C 3317 3495 5.7e-65 PFAM
Pfam:ATG_C 3498 3588 7.9e-12 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000213168
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the vacuolar protein sorting-associated 13 gene family. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010]
Allele List at MGI

All alleles(13) : Targeted, other(2) Gene trapped(11)

Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921511C20Rik T A X: 126,302,584 (GRCm39) Y174* probably null Het
Apc C A 18: 34,446,935 (GRCm39) S1243* probably null Het
Atp8b5 A G 4: 43,365,578 (GRCm39) T731A probably benign Het
Bcl2a1c T A 9: 114,159,458 (GRCm39) F79I probably damaging Het
Brip1 G T 11: 85,955,925 (GRCm39) L863I possibly damaging Het
Cbx4 T A 11: 118,972,938 (GRCm39) K146* probably null Het
Ces1a C T 8: 93,766,126 (GRCm39) V163I possibly damaging Het
Ces5a C T 8: 94,255,272 (GRCm39) probably benign Het
Cfhr1 A C 1: 139,484,131 (GRCm39) N128K possibly damaging Het
Clcn3 T C 8: 61,394,391 (GRCm39) D46G probably damaging Het
Cntnap1 T G 11: 101,068,955 (GRCm39) I166S probably benign Het
Cntnap3 A T 13: 64,946,872 (GRCm39) probably benign Het
Cntnap5c T A 17: 58,714,739 (GRCm39) probably benign Het
Ddx23 A T 15: 98,545,430 (GRCm39) V626E probably damaging Het
Dele1 T A 18: 38,394,177 (GRCm39) L458Q probably damaging Het
Gcm2 T C 13: 41,256,477 (GRCm39) Y424C probably benign Het
Gm9964 A G 11: 79,187,196 (GRCm39) F84L probably damaging Het
Grn T A 11: 102,326,930 (GRCm39) D509E probably benign Het
Iho1 G T 9: 108,283,820 (GRCm39) T208K probably benign Het
Kdm5c G A X: 151,029,314 (GRCm39) D343N probably damaging Het
Ly75 C T 2: 60,124,125 (GRCm39) M1717I probably benign Het
Map1a C A 2: 121,129,134 (GRCm39) P133T probably damaging Het
Mpp2 C A 11: 101,950,199 (GRCm39) A552S possibly damaging Het
Mtr T C 13: 12,213,980 (GRCm39) I897M probably damaging Het
Npas3 A T 12: 54,095,550 (GRCm39) I337F probably damaging Het
Nup85 T C 11: 115,472,691 (GRCm39) probably benign Het
Or10a49 A G 7: 108,468,257 (GRCm39) Y35H probably benign Het
Or10al2 T A 17: 37,983,340 (GRCm39) M142K possibly damaging Het
Or2t46 T A 11: 58,472,024 (GRCm39) L118H possibly damaging Het
Or51l4 T A 7: 103,404,700 (GRCm39) I31F possibly damaging Het
Or56a5 T C 7: 104,792,966 (GRCm39) N178S probably damaging Het
Pdia4 A T 6: 47,780,429 (GRCm39) D301E probably benign Het
Phf2 C A 13: 48,982,322 (GRCm39) G134C unknown Het
Polr2h T A 16: 20,539,352 (GRCm39) L76H probably damaging Het
Rbm47 G A 5: 66,184,364 (GRCm39) R80C probably damaging Het
Sfmbt1 T C 14: 30,507,837 (GRCm39) S286P probably damaging Het
Slc5a12 T C 2: 110,447,179 (GRCm39) probably benign Het
Tacc2 T C 7: 130,227,991 (GRCm39) S1559P probably benign Het
Tbc1d16 T G 11: 119,101,372 (GRCm39) H46P probably damaging Het
Tbck A G 3: 132,440,475 (GRCm39) probably benign Het
Tmtc4 A T 14: 123,163,374 (GRCm39) probably null Het
Ttc13 T C 8: 125,417,100 (GRCm39) probably null Het
Ttc17 T C 2: 94,193,130 (GRCm39) probably benign Het
Vmn1r121 T A 7: 20,832,438 (GRCm39) M1L possibly damaging Het
Zan A C 5: 137,445,106 (GRCm39) S1718A unknown Het
Zfp39 G T 11: 58,793,626 (GRCm39) Y37* probably null Het
Zfp407 T C 18: 84,576,766 (GRCm39) N1449S probably damaging Het
Zhx2 C A 15: 57,687,035 (GRCm39) D801E possibly damaging Het
Other mutations in Vps13c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00159:Vps13c APN 9 67,853,281 (GRCm39) missense probably benign 0.20
IGL00336:Vps13c APN 9 67,853,224 (GRCm39) missense probably benign 0.01
IGL00418:Vps13c APN 9 67,783,544 (GRCm39) missense probably damaging 1.00
IGL00481:Vps13c APN 9 67,768,147 (GRCm39) missense probably damaging 1.00
IGL00491:Vps13c APN 9 67,800,418 (GRCm39) missense probably damaging 1.00
IGL00558:Vps13c APN 9 67,845,139 (GRCm39) missense possibly damaging 0.52
IGL00811:Vps13c APN 9 67,855,463 (GRCm39) missense probably damaging 0.99
IGL01011:Vps13c APN 9 67,834,237 (GRCm39) missense probably damaging 0.98
IGL01094:Vps13c APN 9 67,793,566 (GRCm39) missense probably damaging 1.00
IGL01330:Vps13c APN 9 67,871,390 (GRCm39) missense probably damaging 1.00
IGL01402:Vps13c APN 9 67,820,486 (GRCm39) critical splice acceptor site probably null
IGL01404:Vps13c APN 9 67,820,486 (GRCm39) critical splice acceptor site probably null
IGL01470:Vps13c APN 9 67,820,209 (GRCm39) splice site probably benign
IGL01615:Vps13c APN 9 67,863,063 (GRCm39) missense probably benign 0.01
IGL01694:Vps13c APN 9 67,802,631 (GRCm39) missense probably damaging 1.00
IGL01752:Vps13c APN 9 67,855,510 (GRCm39) missense probably damaging 1.00
IGL01810:Vps13c APN 9 67,863,062 (GRCm39) missense probably benign
IGL01954:Vps13c APN 9 67,876,580 (GRCm39) missense probably damaging 0.98
IGL01978:Vps13c APN 9 67,837,925 (GRCm39) missense probably benign 0.03
IGL01998:Vps13c APN 9 67,862,350 (GRCm39) splice site probably null
IGL02201:Vps13c APN 9 67,874,418 (GRCm39) missense probably damaging 1.00
IGL02205:Vps13c APN 9 67,790,736 (GRCm39) missense probably damaging 1.00
IGL02303:Vps13c APN 9 67,852,763 (GRCm39) splice site probably benign
IGL02322:Vps13c APN 9 67,845,183 (GRCm39) missense probably benign 0.02
IGL02474:Vps13c APN 9 67,845,158 (GRCm39) missense probably benign 0.00
IGL02547:Vps13c APN 9 67,815,301 (GRCm39) missense possibly damaging 0.83
IGL02640:Vps13c APN 9 67,793,530 (GRCm39) splice site probably benign
IGL02673:Vps13c APN 9 67,785,380 (GRCm39) missense probably damaging 1.00
IGL02721:Vps13c APN 9 67,871,431 (GRCm39) splice site probably benign
IGL02834:Vps13c APN 9 67,845,137 (GRCm39) missense probably benign
IGL02838:Vps13c APN 9 67,883,133 (GRCm39) missense probably damaging 1.00
IGL03136:Vps13c APN 9 67,857,592 (GRCm39) missense probably damaging 1.00
IGL03137:Vps13c APN 9 67,797,662 (GRCm39) missense probably damaging 1.00
IGL03214:Vps13c APN 9 67,804,477 (GRCm39) missense probably null 0.81
IGL03240:Vps13c APN 9 67,862,329 (GRCm39) missense probably benign
IGL03303:Vps13c APN 9 67,841,786 (GRCm39) missense probably benign 0.27
IGL03336:Vps13c APN 9 67,858,924 (GRCm39) missense possibly damaging 0.76
IGL03366:Vps13c APN 9 67,853,308 (GRCm39) missense probably benign 0.00
Derivative UTSW 9 67,837,904 (GRCm39) missense possibly damaging 0.79
diversion UTSW 9 67,817,515 (GRCm39) missense possibly damaging 0.93
introversion UTSW 9 67,851,328 (GRCm39) missense probably damaging 0.98
Inversion UTSW 9 67,810,121 (GRCm39) critical splice acceptor site probably null
subversion UTSW 9 67,815,334 (GRCm39) missense probably damaging 1.00
Transversion UTSW 9 67,841,783 (GRCm39) missense probably damaging 0.98
3-1:Vps13c UTSW 9 67,843,655 (GRCm39) missense probably benign 0.00
IGL02991:Vps13c UTSW 9 67,821,159 (GRCm39) missense probably damaging 1.00
PIT4802001:Vps13c UTSW 9 67,845,068 (GRCm39) missense probably damaging 1.00
R0008:Vps13c UTSW 9 67,826,544 (GRCm39) missense probably benign
R0206:Vps13c UTSW 9 67,846,444 (GRCm39) splice site probably benign
R0288:Vps13c UTSW 9 67,834,648 (GRCm39) missense probably damaging 0.99
R0324:Vps13c UTSW 9 67,871,591 (GRCm39) missense possibly damaging 0.95
R0347:Vps13c UTSW 9 67,817,515 (GRCm39) missense possibly damaging 0.93
R0374:Vps13c UTSW 9 67,793,528 (GRCm39) splice site probably benign
R0388:Vps13c UTSW 9 67,830,197 (GRCm39) splice site probably benign
R0409:Vps13c UTSW 9 67,858,926 (GRCm39) missense probably benign 0.00
R0440:Vps13c UTSW 9 67,880,143 (GRCm39) missense probably damaging 1.00
R0513:Vps13c UTSW 9 67,838,017 (GRCm39) missense probably benign 0.02
R0520:Vps13c UTSW 9 67,853,133 (GRCm39) missense possibly damaging 0.88
R0569:Vps13c UTSW 9 67,881,001 (GRCm39) missense probably damaging 0.98
R0601:Vps13c UTSW 9 67,834,754 (GRCm39) missense probably benign 0.12
R0659:Vps13c UTSW 9 67,828,217 (GRCm39) missense probably benign 0.11
R0667:Vps13c UTSW 9 67,858,855 (GRCm39) nonsense probably null
R0670:Vps13c UTSW 9 67,833,139 (GRCm39) missense probably benign 0.35
R0698:Vps13c UTSW 9 67,797,005 (GRCm39) missense probably benign 0.45
R0729:Vps13c UTSW 9 67,868,931 (GRCm39) missense probably damaging 1.00
R0781:Vps13c UTSW 9 67,879,285 (GRCm39) missense probably damaging 1.00
R0811:Vps13c UTSW 9 67,841,758 (GRCm39) missense probably benign 0.06
R0812:Vps13c UTSW 9 67,841,758 (GRCm39) missense probably benign 0.06
R0839:Vps13c UTSW 9 67,806,020 (GRCm39) missense probably benign
R1373:Vps13c UTSW 9 67,834,793 (GRCm39) missense probably damaging 0.99
R1396:Vps13c UTSW 9 67,862,304 (GRCm39) missense probably benign 0.00
R1499:Vps13c UTSW 9 67,864,787 (GRCm39) missense probably benign 0.00
R1556:Vps13c UTSW 9 67,837,993 (GRCm39) missense probably damaging 0.98
R1560:Vps13c UTSW 9 67,843,745 (GRCm39) critical splice donor site probably null
R1584:Vps13c UTSW 9 67,800,394 (GRCm39) missense possibly damaging 0.74
R1654:Vps13c UTSW 9 67,858,969 (GRCm39) missense probably damaging 1.00
R1674:Vps13c UTSW 9 67,760,985 (GRCm39) nonsense probably null
R1676:Vps13c UTSW 9 67,834,244 (GRCm39) missense probably benign 0.20
R1695:Vps13c UTSW 9 67,879,357 (GRCm39) nonsense probably null
R1710:Vps13c UTSW 9 67,818,811 (GRCm39) missense probably benign 0.00
R1769:Vps13c UTSW 9 67,873,003 (GRCm39) missense probably benign 0.00
R1775:Vps13c UTSW 9 67,788,729 (GRCm39) missense probably damaging 1.00
R1795:Vps13c UTSW 9 67,801,267 (GRCm39) nonsense probably null
R1799:Vps13c UTSW 9 67,851,399 (GRCm39) missense probably damaging 0.98
R1835:Vps13c UTSW 9 67,900,295 (GRCm39) missense probably benign 0.08
R1848:Vps13c UTSW 9 67,843,622 (GRCm39) missense probably benign
R1903:Vps13c UTSW 9 67,801,334 (GRCm39) missense probably damaging 1.00
R1944:Vps13c UTSW 9 67,793,558 (GRCm39) missense probably damaging 1.00
R1945:Vps13c UTSW 9 67,793,558 (GRCm39) missense probably damaging 1.00
R1951:Vps13c UTSW 9 67,881,041 (GRCm39) critical splice donor site probably null
R1993:Vps13c UTSW 9 67,883,138 (GRCm39) missense probably damaging 1.00
R2023:Vps13c UTSW 9 67,843,567 (GRCm39) splice site probably benign
R2059:Vps13c UTSW 9 67,768,115 (GRCm39) missense probably damaging 1.00
R2086:Vps13c UTSW 9 67,857,571 (GRCm39) missense probably benign 0.29
R2120:Vps13c UTSW 9 67,826,616 (GRCm39) missense possibly damaging 0.92
R2249:Vps13c UTSW 9 67,895,335 (GRCm39) critical splice donor site probably null
R2257:Vps13c UTSW 9 67,860,228 (GRCm39) missense possibly damaging 0.87
R2258:Vps13c UTSW 9 67,861,142 (GRCm39) missense probably benign 0.01
R2259:Vps13c UTSW 9 67,861,142 (GRCm39) missense probably benign 0.01
R2260:Vps13c UTSW 9 67,861,142 (GRCm39) missense probably benign 0.01
R2265:Vps13c UTSW 9 67,828,229 (GRCm39) missense possibly damaging 0.82
R2266:Vps13c UTSW 9 67,828,229 (GRCm39) missense possibly damaging 0.82
R2269:Vps13c UTSW 9 67,828,229 (GRCm39) missense possibly damaging 0.82
R2278:Vps13c UTSW 9 67,846,354 (GRCm39) missense probably benign
R2306:Vps13c UTSW 9 67,895,275 (GRCm39) missense probably damaging 0.99
R2327:Vps13c UTSW 9 67,821,102 (GRCm39) missense probably damaging 0.98
R2349:Vps13c UTSW 9 67,864,808 (GRCm39) missense possibly damaging 0.89
R2483:Vps13c UTSW 9 67,883,189 (GRCm39) critical splice donor site probably null
R3031:Vps13c UTSW 9 67,831,052 (GRCm39) missense probably benign 0.00
R3623:Vps13c UTSW 9 67,883,189 (GRCm39) critical splice donor site probably null
R3870:Vps13c UTSW 9 67,792,008 (GRCm39) missense probably benign 0.00
R4173:Vps13c UTSW 9 67,843,595 (GRCm39) missense probably benign 0.00
R4445:Vps13c UTSW 9 67,889,777 (GRCm39) splice site probably null
R4491:Vps13c UTSW 9 67,817,475 (GRCm39) missense probably benign
R4505:Vps13c UTSW 9 67,846,316 (GRCm39) missense probably benign 0.02
R4574:Vps13c UTSW 9 67,858,965 (GRCm39) missense probably damaging 1.00
R4691:Vps13c UTSW 9 67,860,217 (GRCm39) missense possibly damaging 0.95
R4766:Vps13c UTSW 9 67,785,506 (GRCm39) splice site probably null
R4771:Vps13c UTSW 9 67,836,821 (GRCm39) missense probably benign
R4801:Vps13c UTSW 9 67,871,564 (GRCm39) missense probably damaging 1.00
R4802:Vps13c UTSW 9 67,871,564 (GRCm39) missense probably damaging 1.00
R4962:Vps13c UTSW 9 67,781,173 (GRCm39) missense probably damaging 1.00
R4995:Vps13c UTSW 9 67,826,603 (GRCm39) missense probably benign 0.00
R5010:Vps13c UTSW 9 67,823,661 (GRCm39) missense probably benign 0.19
R5183:Vps13c UTSW 9 67,815,334 (GRCm39) missense probably damaging 1.00
R5226:Vps13c UTSW 9 67,852,835 (GRCm39) missense probably benign 0.17
R5297:Vps13c UTSW 9 67,785,413 (GRCm39) missense probably damaging 1.00
R5456:Vps13c UTSW 9 67,834,729 (GRCm39) missense possibly damaging 0.53
R5494:Vps13c UTSW 9 67,855,428 (GRCm39) missense probably benign 0.00
R5521:Vps13c UTSW 9 67,858,721 (GRCm39) missense probably benign 0.08
R5524:Vps13c UTSW 9 67,864,838 (GRCm39) missense probably damaging 1.00
R5685:Vps13c UTSW 9 67,870,455 (GRCm39) missense possibly damaging 0.64
R5731:Vps13c UTSW 9 67,802,661 (GRCm39) missense probably damaging 1.00
R5812:Vps13c UTSW 9 67,889,777 (GRCm39) splice site probably benign
R5867:Vps13c UTSW 9 67,889,904 (GRCm39) splice site probably null
R5893:Vps13c UTSW 9 67,810,121 (GRCm39) critical splice acceptor site probably null
R5902:Vps13c UTSW 9 67,841,729 (GRCm39) missense probably benign 0.00
R5957:Vps13c UTSW 9 67,862,253 (GRCm39) missense probably damaging 1.00
R6076:Vps13c UTSW 9 67,818,884 (GRCm39) missense probably damaging 1.00
R6187:Vps13c UTSW 9 67,822,939 (GRCm39) missense probably damaging 1.00
R6268:Vps13c UTSW 9 67,858,731 (GRCm39) missense probably benign 0.10
R6547:Vps13c UTSW 9 67,880,647 (GRCm39) missense probably damaging 1.00
R6716:Vps13c UTSW 9 67,858,749 (GRCm39) missense probably benign 0.00
R6837:Vps13c UTSW 9 67,817,504 (GRCm39) missense probably benign
R6919:Vps13c UTSW 9 67,834,734 (GRCm39) missense probably damaging 0.97
R7039:Vps13c UTSW 9 67,845,045 (GRCm39) missense probably damaging 1.00
R7058:Vps13c UTSW 9 67,831,110 (GRCm39) missense probably benign 0.39
R7082:Vps13c UTSW 9 67,790,735 (GRCm39) missense probably damaging 1.00
R7195:Vps13c UTSW 9 67,853,107 (GRCm39) missense possibly damaging 0.95
R7244:Vps13c UTSW 9 67,797,086 (GRCm39) missense probably benign 0.00
R7300:Vps13c UTSW 9 67,847,826 (GRCm39) missense probably benign 0.20
R7314:Vps13c UTSW 9 67,850,622 (GRCm39) splice site probably null
R7352:Vps13c UTSW 9 67,747,728 (GRCm39) missense possibly damaging 0.94
R7368:Vps13c UTSW 9 67,821,355 (GRCm39) missense probably benign 0.23
R7411:Vps13c UTSW 9 67,879,283 (GRCm39) missense probably damaging 0.98
R7497:Vps13c UTSW 9 67,747,761 (GRCm39) missense probably damaging 1.00
R7516:Vps13c UTSW 9 67,862,289 (GRCm39) missense possibly damaging 0.89
R7638:Vps13c UTSW 9 67,852,791 (GRCm39) missense probably damaging 1.00
R7732:Vps13c UTSW 9 67,847,798 (GRCm39) missense probably damaging 0.97
R7748:Vps13c UTSW 9 67,870,371 (GRCm39) missense probably benign 0.03
R7779:Vps13c UTSW 9 67,788,704 (GRCm39) missense probably damaging 1.00
R7788:Vps13c UTSW 9 67,847,765 (GRCm39) missense probably benign 0.01
R7894:Vps13c UTSW 9 67,834,265 (GRCm39) missense probably damaging 0.99
R8163:Vps13c UTSW 9 67,857,720 (GRCm39) missense probably benign 0.08
R8165:Vps13c UTSW 9 67,766,072 (GRCm39) missense probably benign 0.00
R8202:Vps13c UTSW 9 67,851,328 (GRCm39) missense probably damaging 0.98
R8235:Vps13c UTSW 9 67,863,063 (GRCm39) missense probably benign 0.01
R8235:Vps13c UTSW 9 67,834,678 (GRCm39) missense probably damaging 1.00
R8253:Vps13c UTSW 9 67,850,770 (GRCm39) nonsense probably null
R8261:Vps13c UTSW 9 67,862,262 (GRCm39) missense probably damaging 1.00
R8348:Vps13c UTSW 9 67,786,385 (GRCm39) missense possibly damaging 0.79
R8547:Vps13c UTSW 9 67,852,848 (GRCm39) missense probably damaging 1.00
R8734:Vps13c UTSW 9 67,880,685 (GRCm39) missense probably damaging 1.00
R8806:Vps13c UTSW 9 67,853,110 (GRCm39) missense probably damaging 1.00
R8807:Vps13c UTSW 9 67,766,122 (GRCm39) missense probably damaging 0.99
R8813:Vps13c UTSW 9 67,778,566 (GRCm39) missense probably damaging 1.00
R8883:Vps13c UTSW 9 67,855,479 (GRCm39) missense probably benign 0.10
R8885:Vps13c UTSW 9 67,850,736 (GRCm39) missense probably benign
R8899:Vps13c UTSW 9 67,841,783 (GRCm39) missense probably damaging 0.98
R8970:Vps13c UTSW 9 67,852,803 (GRCm39) missense probably benign 0.11
R9007:Vps13c UTSW 9 67,845,006 (GRCm39) missense probably benign 0.00
R9026:Vps13c UTSW 9 67,861,863 (GRCm39) missense probably damaging 1.00
R9029:Vps13c UTSW 9 67,855,429 (GRCm39) missense probably damaging 0.98
R9057:Vps13c UTSW 9 67,828,209 (GRCm39) missense probably benign 0.00
R9105:Vps13c UTSW 9 67,778,081 (GRCm39) intron probably benign
R9130:Vps13c UTSW 9 67,836,805 (GRCm39) missense probably damaging 1.00
R9286:Vps13c UTSW 9 67,880,203 (GRCm39) missense probably benign 0.00
R9338:Vps13c UTSW 9 67,858,977 (GRCm39) missense probably damaging 1.00
R9432:Vps13c UTSW 9 67,830,137 (GRCm39) missense probably benign 0.02
R9460:Vps13c UTSW 9 67,837,904 (GRCm39) missense possibly damaging 0.79
R9464:Vps13c UTSW 9 67,858,674 (GRCm39) missense probably damaging 1.00
R9561:Vps13c UTSW 9 67,872,794 (GRCm39) missense probably damaging 1.00
R9609:Vps13c UTSW 9 67,841,831 (GRCm39) missense probably damaging 1.00
R9622:Vps13c UTSW 9 67,856,715 (GRCm39) missense probably damaging 1.00
R9665:Vps13c UTSW 9 67,863,025 (GRCm39) nonsense probably null
R9731:Vps13c UTSW 9 67,826,526 (GRCm39) missense probably benign
R9763:Vps13c UTSW 9 67,818,860 (GRCm39) missense probably benign 0.00
R9774:Vps13c UTSW 9 67,791,873 (GRCm39) missense possibly damaging 0.85
R9798:Vps13c UTSW 9 67,826,646 (GRCm39) missense probably damaging 1.00
U24488:Vps13c UTSW 9 67,813,198 (GRCm39) missense probably benign 0.13
X0021:Vps13c UTSW 9 67,845,063 (GRCm39) missense probably damaging 0.99
X0058:Vps13c UTSW 9 67,834,701 (GRCm39) missense probably damaging 1.00
X0065:Vps13c UTSW 9 67,781,145 (GRCm39) missense probably damaging 1.00
Z1088:Vps13c UTSW 9 67,821,257 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16