Incidental Mutation 'IGL01978:Vps13c'
ID 181780
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Vps13c
Ensembl Gene ENSMUSG00000035284
Gene Name vacuolar protein sorting 13C
Synonyms C230055H22Rik
Accession Numbers

Genbank: NM_177184; MGI: 2444207

Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL01978
Quality Score
Status
Chromosome 9
Chromosomal Location 67840396-67995638 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 67930643 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 1825 (H1825R)
Ref Sequence ENSEMBL: ENSMUSP00000077040 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077879]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000077879
AA Change: H1825R

PolyPhen 2 Score 0.025 (Sensitivity: 0.95; Specificity: 0.81)
SMART Domains Protein: ENSMUSP00000077040
Gene: ENSMUSG00000035284
AA Change: H1825R

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
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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2410089E03Rik A T 15: 8,219,382 (GRCm38) N1805I probably damaging Het
9830107B12Rik T A 17: 48,145,993 (GRCm38) T6S probably damaging Het
Acot5 T C 12: 84,075,398 (GRCm38) V252A possibly damaging Het
Bmper A T 9: 23,381,441 (GRCm38) N349Y probably damaging Het
Brap A G 5: 121,678,847 (GRCm38) probably benign Het
Col9a2 G A 4: 121,044,666 (GRCm38) G139E unknown Het
Cyp2j8 A C 4: 96,504,009 (GRCm38) probably null Het
Dcbld2 A G 16: 58,464,319 (GRCm38) D612G probably benign Het
Dsc3 C T 18: 19,974,196 (GRCm38) R456Q possibly damaging Het
Fat2 T C 11: 55,270,146 (GRCm38) T3253A probably benign Het
Hoxc12 T A 15: 102,936,864 (GRCm38) H4Q probably damaging Het
Il6st A G 13: 112,497,357 (GRCm38) E445G possibly damaging Het
Ipo8 T C 6: 148,777,289 (GRCm38) E937G probably benign Het
Kif5a A C 10: 127,245,739 (GRCm38) D185E probably benign Het
Klhl38 T C 15: 58,315,089 (GRCm38) D495G probably damaging Het
Klra5 A G 6: 129,911,430 (GRCm38) V11A probably benign Het
Lrch1 G A 14: 74,786,342 (GRCm38) T581M probably damaging Het
Mecom A G 3: 29,963,166 (GRCm38) I450T probably damaging Het
Mrgprb2 C A 7: 48,552,564 (GRCm38) V138L probably damaging Het
Muc15 G A 2: 110,731,596 (GRCm38) A126T probably benign Het
Mybpc1 A T 10: 88,531,770 (GRCm38) I522K probably damaging Het
Nectin1 G A 9: 43,792,147 (GRCm38) R234H probably damaging Het
Olfr1450 T C 19: 12,954,042 (GRCm38) F151S probably benign Het
Olfr190 A T 16: 59,074,267 (GRCm38) I271K probably benign Het
Pdia6 T A 12: 17,274,422 (GRCm38) H91Q possibly damaging Het
Pfkfb4 A T 9: 109,028,942 (GRCm38) H445L probably damaging Het
Pkd1l1 T C 11: 8,961,336 (GRCm38) T314A unknown Het
Rb1cc1 A G 1: 6,238,368 (GRCm38) D159G probably damaging Het
Rhoh T A 5: 65,892,688 (GRCm38) S100R probably benign Het
Rsbn1 T A 3: 103,961,500 (GRCm38) D618E probably damaging Het
Slc25a47 T C 12: 108,851,190 (GRCm38) V4A probably damaging Het
Svs3b T A 2: 164,256,621 (GRCm38) M1L probably benign Het
Thsd7a T C 6: 12,331,006 (GRCm38) N1379S probably benign Het
Tmed3 T C 9: 89,704,753 (GRCm38) D58G probably benign Het
Trh G A 6: 92,242,615 (GRCm38) A240V probably benign Het
Ubox5 A T 2: 130,600,452 (GRCm38) V105E probably benign Het
Vmn2r67 A G 7: 85,151,441 (GRCm38) probably null Het
Wasf1 C A 10: 40,936,201 (GRCm38) P329T unknown Het
Wee2 T C 6: 40,455,153 (GRCm38) F219L probably damaging Het
Zp3r T C 1: 130,598,941 (GRCm38) D175G probably damaging Het
Other mutations in Vps13c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00159:Vps13c APN 9 67,945,999 (GRCm38) missense probably benign 0.20
IGL00336:Vps13c APN 9 67,945,942 (GRCm38) missense probably benign 0.01
IGL00418:Vps13c APN 9 67,876,262 (GRCm38) missense probably damaging 1.00
IGL00481:Vps13c APN 9 67,860,865 (GRCm38) missense probably damaging 1.00
IGL00491:Vps13c APN 9 67,893,136 (GRCm38) missense probably damaging 1.00
IGL00558:Vps13c APN 9 67,937,857 (GRCm38) missense possibly damaging 0.52
IGL00811:Vps13c APN 9 67,948,181 (GRCm38) missense probably damaging 0.99
IGL01011:Vps13c APN 9 67,926,955 (GRCm38) missense probably damaging 0.98
IGL01094:Vps13c APN 9 67,886,284 (GRCm38) missense probably damaging 1.00
IGL01330:Vps13c APN 9 67,964,108 (GRCm38) missense probably damaging 1.00
IGL01402:Vps13c APN 9 67,913,204 (GRCm38) critical splice acceptor site probably null
IGL01404:Vps13c APN 9 67,913,204 (GRCm38) critical splice acceptor site probably null
IGL01470:Vps13c APN 9 67,912,927 (GRCm38) splice site probably benign
IGL01615:Vps13c APN 9 67,955,781 (GRCm38) missense probably benign 0.01
IGL01694:Vps13c APN 9 67,895,349 (GRCm38) missense probably damaging 1.00
IGL01752:Vps13c APN 9 67,948,228 (GRCm38) missense probably damaging 1.00
IGL01810:Vps13c APN 9 67,955,780 (GRCm38) missense probably benign
IGL01954:Vps13c APN 9 67,969,298 (GRCm38) missense probably damaging 0.98
IGL01998:Vps13c APN 9 67,955,068 (GRCm38) splice site probably null
IGL02201:Vps13c APN 9 67,967,136 (GRCm38) missense probably damaging 1.00
IGL02205:Vps13c APN 9 67,883,454 (GRCm38) missense probably damaging 1.00
IGL02303:Vps13c APN 9 67,945,481 (GRCm38) splice site probably benign
IGL02322:Vps13c APN 9 67,937,901 (GRCm38) missense probably benign 0.02
IGL02456:Vps13c APN 9 67,952,976 (GRCm38) missense probably damaging 1.00
IGL02474:Vps13c APN 9 67,937,876 (GRCm38) missense probably benign 0.00
IGL02547:Vps13c APN 9 67,908,019 (GRCm38) missense possibly damaging 0.83
IGL02640:Vps13c APN 9 67,886,248 (GRCm38) splice site probably benign
IGL02673:Vps13c APN 9 67,878,098 (GRCm38) missense probably damaging 1.00
IGL02721:Vps13c APN 9 67,964,149 (GRCm38) splice site probably benign
IGL02834:Vps13c APN 9 67,937,855 (GRCm38) missense probably benign
IGL02838:Vps13c APN 9 67,975,851 (GRCm38) missense probably damaging 1.00
IGL03136:Vps13c APN 9 67,950,310 (GRCm38) missense probably damaging 1.00
IGL03137:Vps13c APN 9 67,890,380 (GRCm38) missense probably damaging 1.00
IGL03214:Vps13c APN 9 67,897,195 (GRCm38) missense probably null 0.81
IGL03240:Vps13c APN 9 67,955,047 (GRCm38) missense probably benign
IGL03303:Vps13c APN 9 67,934,504 (GRCm38) missense probably benign 0.27
IGL03336:Vps13c APN 9 67,951,642 (GRCm38) missense possibly damaging 0.76
IGL03366:Vps13c APN 9 67,946,026 (GRCm38) missense probably benign 0.00
Derivative UTSW 9 67,930,622 (GRCm38) missense possibly damaging 0.79
diversion UTSW 9 67,910,233 (GRCm38) missense possibly damaging 0.93
introversion UTSW 9 67,944,046 (GRCm38) missense probably damaging 0.98
Inversion UTSW 9 67,902,839 (GRCm38) critical splice acceptor site probably null
subversion UTSW 9 67,908,052 (GRCm38) missense probably damaging 1.00
Transversion UTSW 9 67,934,501 (GRCm38) missense probably damaging 0.98
3-1:Vps13c UTSW 9 67,936,373 (GRCm38) missense probably benign 0.00
IGL02991:Vps13c UTSW 9 67,913,877 (GRCm38) missense probably damaging 1.00
PIT4802001:Vps13c UTSW 9 67,937,786 (GRCm38) missense probably damaging 1.00
R0008:Vps13c UTSW 9 67,919,262 (GRCm38) missense probably benign
R0206:Vps13c UTSW 9 67,939,162 (GRCm38) splice site probably benign
R0288:Vps13c UTSW 9 67,927,366 (GRCm38) missense probably damaging 0.99
R0324:Vps13c UTSW 9 67,964,309 (GRCm38) missense possibly damaging 0.95
R0347:Vps13c UTSW 9 67,910,233 (GRCm38) missense possibly damaging 0.93
R0374:Vps13c UTSW 9 67,886,246 (GRCm38) splice site probably benign
R0388:Vps13c UTSW 9 67,922,915 (GRCm38) splice site probably benign
R0409:Vps13c UTSW 9 67,951,644 (GRCm38) missense probably benign 0.00
R0440:Vps13c UTSW 9 67,972,861 (GRCm38) missense probably damaging 1.00
R0513:Vps13c UTSW 9 67,930,735 (GRCm38) missense probably benign 0.02
R0520:Vps13c UTSW 9 67,945,851 (GRCm38) missense possibly damaging 0.88
R0569:Vps13c UTSW 9 67,973,719 (GRCm38) missense probably damaging 0.98
R0601:Vps13c UTSW 9 67,927,472 (GRCm38) missense probably benign 0.12
R0659:Vps13c UTSW 9 67,920,935 (GRCm38) missense probably benign 0.11
R0667:Vps13c UTSW 9 67,951,573 (GRCm38) nonsense probably null
R0670:Vps13c UTSW 9 67,925,857 (GRCm38) missense probably benign 0.35
R0698:Vps13c UTSW 9 67,889,723 (GRCm38) missense probably benign 0.45
R0729:Vps13c UTSW 9 67,961,649 (GRCm38) missense probably damaging 1.00
R0781:Vps13c UTSW 9 67,972,003 (GRCm38) missense probably damaging 1.00
R0811:Vps13c UTSW 9 67,934,476 (GRCm38) missense probably benign 0.06
R0812:Vps13c UTSW 9 67,934,476 (GRCm38) missense probably benign 0.06
R0839:Vps13c UTSW 9 67,898,738 (GRCm38) missense probably benign
R1373:Vps13c UTSW 9 67,927,511 (GRCm38) missense probably damaging 0.99
R1396:Vps13c UTSW 9 67,955,022 (GRCm38) missense probably benign 0.00
R1499:Vps13c UTSW 9 67,957,505 (GRCm38) missense probably benign 0.00
R1556:Vps13c UTSW 9 67,930,711 (GRCm38) missense probably damaging 0.98
R1560:Vps13c UTSW 9 67,936,463 (GRCm38) critical splice donor site probably null
R1584:Vps13c UTSW 9 67,893,112 (GRCm38) missense possibly damaging 0.74
R1654:Vps13c UTSW 9 67,951,687 (GRCm38) missense probably damaging 1.00
R1674:Vps13c UTSW 9 67,853,703 (GRCm38) nonsense probably null
R1676:Vps13c UTSW 9 67,926,962 (GRCm38) missense probably benign 0.20
R1695:Vps13c UTSW 9 67,972,075 (GRCm38) nonsense probably null
R1710:Vps13c UTSW 9 67,911,529 (GRCm38) missense probably benign 0.00
R1769:Vps13c UTSW 9 67,965,721 (GRCm38) missense probably benign 0.00
R1775:Vps13c UTSW 9 67,881,447 (GRCm38) missense probably damaging 1.00
R1795:Vps13c UTSW 9 67,893,985 (GRCm38) nonsense probably null
R1799:Vps13c UTSW 9 67,944,117 (GRCm38) missense probably damaging 0.98
R1835:Vps13c UTSW 9 67,993,013 (GRCm38) missense probably benign 0.08
R1848:Vps13c UTSW 9 67,936,340 (GRCm38) missense probably benign
R1903:Vps13c UTSW 9 67,894,052 (GRCm38) missense probably damaging 1.00
R1944:Vps13c UTSW 9 67,886,276 (GRCm38) missense probably damaging 1.00
R1945:Vps13c UTSW 9 67,886,276 (GRCm38) missense probably damaging 1.00
R1951:Vps13c UTSW 9 67,973,759 (GRCm38) critical splice donor site probably null
R1993:Vps13c UTSW 9 67,975,856 (GRCm38) missense probably damaging 1.00
R2023:Vps13c UTSW 9 67,936,285 (GRCm38) splice site probably benign
R2059:Vps13c UTSW 9 67,860,833 (GRCm38) missense probably damaging 1.00
R2086:Vps13c UTSW 9 67,950,289 (GRCm38) missense probably benign 0.29
R2120:Vps13c UTSW 9 67,919,334 (GRCm38) missense possibly damaging 0.92
R2249:Vps13c UTSW 9 67,988,053 (GRCm38) critical splice donor site probably null
R2257:Vps13c UTSW 9 67,952,946 (GRCm38) missense possibly damaging 0.87
R2258:Vps13c UTSW 9 67,953,860 (GRCm38) missense probably benign 0.01
R2259:Vps13c UTSW 9 67,953,860 (GRCm38) missense probably benign 0.01
R2260:Vps13c UTSW 9 67,953,860 (GRCm38) missense probably benign 0.01
R2265:Vps13c UTSW 9 67,920,947 (GRCm38) missense possibly damaging 0.82
R2266:Vps13c UTSW 9 67,920,947 (GRCm38) missense possibly damaging 0.82
R2269:Vps13c UTSW 9 67,920,947 (GRCm38) missense possibly damaging 0.82
R2278:Vps13c UTSW 9 67,939,072 (GRCm38) missense probably benign
R2306:Vps13c UTSW 9 67,987,993 (GRCm38) missense probably damaging 0.99
R2327:Vps13c UTSW 9 67,913,820 (GRCm38) missense probably damaging 0.98
R2349:Vps13c UTSW 9 67,957,526 (GRCm38) missense possibly damaging 0.89
R2483:Vps13c UTSW 9 67,975,907 (GRCm38) critical splice donor site probably null
R3031:Vps13c UTSW 9 67,923,770 (GRCm38) missense probably benign 0.00
R3623:Vps13c UTSW 9 67,975,907 (GRCm38) critical splice donor site probably null
R3870:Vps13c UTSW 9 67,884,726 (GRCm38) missense probably benign 0.00
R4173:Vps13c UTSW 9 67,936,313 (GRCm38) missense probably benign 0.00
R4445:Vps13c UTSW 9 67,982,495 (GRCm38) splice site probably null
R4491:Vps13c UTSW 9 67,910,193 (GRCm38) missense probably benign
R4505:Vps13c UTSW 9 67,939,034 (GRCm38) missense probably benign 0.02
R4574:Vps13c UTSW 9 67,951,683 (GRCm38) missense probably damaging 1.00
R4691:Vps13c UTSW 9 67,952,935 (GRCm38) missense possibly damaging 0.95
R4766:Vps13c UTSW 9 67,878,224 (GRCm38) splice site probably null
R4771:Vps13c UTSW 9 67,929,539 (GRCm38) missense probably benign
R4801:Vps13c UTSW 9 67,964,282 (GRCm38) missense probably damaging 1.00
R4802:Vps13c UTSW 9 67,964,282 (GRCm38) missense probably damaging 1.00
R4962:Vps13c UTSW 9 67,873,891 (GRCm38) missense probably damaging 1.00
R4995:Vps13c UTSW 9 67,919,321 (GRCm38) missense probably benign 0.00
R5010:Vps13c UTSW 9 67,916,379 (GRCm38) missense probably benign 0.19
R5183:Vps13c UTSW 9 67,908,052 (GRCm38) missense probably damaging 1.00
R5226:Vps13c UTSW 9 67,945,553 (GRCm38) missense probably benign 0.17
R5297:Vps13c UTSW 9 67,878,131 (GRCm38) missense probably damaging 1.00
R5456:Vps13c UTSW 9 67,927,447 (GRCm38) missense possibly damaging 0.53
R5494:Vps13c UTSW 9 67,948,146 (GRCm38) missense probably benign 0.00
R5521:Vps13c UTSW 9 67,951,439 (GRCm38) missense probably benign 0.08
R5524:Vps13c UTSW 9 67,957,556 (GRCm38) missense probably damaging 1.00
R5685:Vps13c UTSW 9 67,963,173 (GRCm38) missense possibly damaging 0.64
R5731:Vps13c UTSW 9 67,895,379 (GRCm38) missense probably damaging 1.00
R5812:Vps13c UTSW 9 67,982,495 (GRCm38) splice site probably benign
R5867:Vps13c UTSW 9 67,982,622 (GRCm38) splice site probably null
R5893:Vps13c UTSW 9 67,902,839 (GRCm38) critical splice acceptor site probably null
R5902:Vps13c UTSW 9 67,934,447 (GRCm38) missense probably benign 0.00
R5957:Vps13c UTSW 9 67,954,971 (GRCm38) missense probably damaging 1.00
R6076:Vps13c UTSW 9 67,911,602 (GRCm38) missense probably damaging 1.00
R6187:Vps13c UTSW 9 67,915,657 (GRCm38) missense probably damaging 1.00
R6268:Vps13c UTSW 9 67,951,449 (GRCm38) missense probably benign 0.10
R6547:Vps13c UTSW 9 67,973,365 (GRCm38) missense probably damaging 1.00
R6716:Vps13c UTSW 9 67,951,467 (GRCm38) missense probably benign 0.00
R6837:Vps13c UTSW 9 67,910,222 (GRCm38) missense probably benign
R6919:Vps13c UTSW 9 67,927,452 (GRCm38) missense probably damaging 0.97
R7039:Vps13c UTSW 9 67,937,763 (GRCm38) missense probably damaging 1.00
R7058:Vps13c UTSW 9 67,923,828 (GRCm38) missense probably benign 0.39
R7082:Vps13c UTSW 9 67,883,453 (GRCm38) missense probably damaging 1.00
R7195:Vps13c UTSW 9 67,945,825 (GRCm38) missense possibly damaging 0.95
R7244:Vps13c UTSW 9 67,889,804 (GRCm38) missense probably benign 0.00
R7300:Vps13c UTSW 9 67,940,544 (GRCm38) missense probably benign 0.20
R7314:Vps13c UTSW 9 67,943,340 (GRCm38) splice site probably null
R7352:Vps13c UTSW 9 67,840,446 (GRCm38) missense possibly damaging 0.94
R7368:Vps13c UTSW 9 67,914,073 (GRCm38) missense probably benign 0.23
R7411:Vps13c UTSW 9 67,972,001 (GRCm38) missense probably damaging 0.98
R7497:Vps13c UTSW 9 67,840,479 (GRCm38) missense probably damaging 1.00
R7516:Vps13c UTSW 9 67,955,007 (GRCm38) missense possibly damaging 0.89
R7638:Vps13c UTSW 9 67,945,509 (GRCm38) missense probably damaging 1.00
R7732:Vps13c UTSW 9 67,940,516 (GRCm38) missense probably damaging 0.97
R7748:Vps13c UTSW 9 67,963,089 (GRCm38) missense probably benign 0.03
R7779:Vps13c UTSW 9 67,881,422 (GRCm38) missense probably damaging 1.00
R7788:Vps13c UTSW 9 67,940,483 (GRCm38) missense probably benign 0.01
R7894:Vps13c UTSW 9 67,926,983 (GRCm38) missense probably damaging 0.99
R8163:Vps13c UTSW 9 67,950,438 (GRCm38) missense probably benign 0.08
R8165:Vps13c UTSW 9 67,858,790 (GRCm38) missense probably benign 0.00
R8202:Vps13c UTSW 9 67,944,046 (GRCm38) missense probably damaging 0.98
R8235:Vps13c UTSW 9 67,955,781 (GRCm38) missense probably benign 0.01
R8235:Vps13c UTSW 9 67,927,396 (GRCm38) missense probably damaging 1.00
R8253:Vps13c UTSW 9 67,943,488 (GRCm38) nonsense probably null
R8261:Vps13c UTSW 9 67,954,980 (GRCm38) missense probably damaging 1.00
R8348:Vps13c UTSW 9 67,879,103 (GRCm38) missense possibly damaging 0.79
R8547:Vps13c UTSW 9 67,945,566 (GRCm38) missense probably damaging 1.00
R8734:Vps13c UTSW 9 67,973,403 (GRCm38) missense probably damaging 1.00
R8806:Vps13c UTSW 9 67,945,828 (GRCm38) missense probably damaging 1.00
R8807:Vps13c UTSW 9 67,858,840 (GRCm38) missense probably damaging 0.99
R8813:Vps13c UTSW 9 67,871,284 (GRCm38) missense probably damaging 1.00
R8883:Vps13c UTSW 9 67,948,197 (GRCm38) missense probably benign 0.10
R8885:Vps13c UTSW 9 67,943,454 (GRCm38) missense probably benign
R8899:Vps13c UTSW 9 67,934,501 (GRCm38) missense probably damaging 0.98
R8970:Vps13c UTSW 9 67,945,521 (GRCm38) missense probably benign 0.11
R9007:Vps13c UTSW 9 67,937,724 (GRCm38) missense probably benign 0.00
R9026:Vps13c UTSW 9 67,954,581 (GRCm38) missense probably damaging 1.00
R9029:Vps13c UTSW 9 67,948,147 (GRCm38) missense probably damaging 0.98
R9057:Vps13c UTSW 9 67,920,927 (GRCm38) missense probably benign 0.00
R9105:Vps13c UTSW 9 67,870,799 (GRCm38) intron probably benign
R9130:Vps13c UTSW 9 67,929,523 (GRCm38) missense probably damaging 1.00
R9286:Vps13c UTSW 9 67,972,921 (GRCm38) missense probably benign 0.00
R9338:Vps13c UTSW 9 67,951,695 (GRCm38) missense probably damaging 1.00
R9432:Vps13c UTSW 9 67,922,855 (GRCm38) missense probably benign 0.02
R9460:Vps13c UTSW 9 67,930,622 (GRCm38) missense possibly damaging 0.79
R9464:Vps13c UTSW 9 67,951,392 (GRCm38) missense probably damaging 1.00
R9561:Vps13c UTSW 9 67,965,512 (GRCm38) missense probably damaging 1.00
R9609:Vps13c UTSW 9 67,934,549 (GRCm38) missense probably damaging 1.00
R9622:Vps13c UTSW 9 67,949,433 (GRCm38) missense probably damaging 1.00
R9665:Vps13c UTSW 9 67,955,743 (GRCm38) nonsense probably null
R9731:Vps13c UTSW 9 67,919,244 (GRCm38) missense probably benign
R9763:Vps13c UTSW 9 67,911,578 (GRCm38) missense probably benign 0.00
R9774:Vps13c UTSW 9 67,884,591 (GRCm38) missense possibly damaging 0.85
R9798:Vps13c UTSW 9 67,919,364 (GRCm38) missense probably damaging 1.00
U24488:Vps13c UTSW 9 67,905,916 (GRCm38) missense probably benign 0.13
X0021:Vps13c UTSW 9 67,937,781 (GRCm38) missense probably damaging 0.99
X0058:Vps13c UTSW 9 67,927,419 (GRCm38) missense probably damaging 1.00
X0065:Vps13c UTSW 9 67,873,863 (GRCm38) missense probably damaging 1.00
Z1088:Vps13c UTSW 9 67,913,975 (GRCm38) missense probably damaging 1.00
Posted On 2014-05-07