Incidental Mutation 'IGL00489:Aspm'
ID |
9096 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Aspm
|
Ensembl Gene |
ENSMUSG00000033952 |
Gene Name |
abnormal spindle microtubule assembly |
Synonyms |
Aspm, Sha1, MCPH5, D330028K02Rik, Calmbp1 |
Accession Numbers |
Genbank: NM_009791; MGI: 1334448 |
Is this an essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL00489
|
Quality Score |
|
Status
|
|
Chromosome |
1 |
Chromosomal Location |
139454772-139494091 bp(+) (GRCm38) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 139478691 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Alanine to Glutamic Acid
at position 1772
(A1772E)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000059159
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000053364]
[ENSMUST00000200083]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000053364
AA Change: A1772E
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000059159 Gene: ENSMUSG00000033952 AA Change: A1772E
Domain | Start | End | E-Value | Type |
Pfam:ASH
|
29 |
126 |
8.9e-35 |
PFAM |
low complexity region
|
855 |
861 |
N/A |
INTRINSIC |
CH
|
890 |
1022 |
2.04e0 |
SMART |
CH
|
1080 |
1224 |
5.56e-9 |
SMART |
IQ
|
1233 |
1255 |
7.57e0 |
SMART |
IQ
|
1259 |
1281 |
1.12e1 |
SMART |
IQ
|
1282 |
1304 |
3.73e-1 |
SMART |
IQ
|
1314 |
1336 |
2.41e-4 |
SMART |
IQ
|
1360 |
1382 |
2.12e1 |
SMART |
IQ
|
1387 |
1408 |
7.61e1 |
SMART |
IQ
|
1409 |
1431 |
6.97e0 |
SMART |
IQ
|
1432 |
1452 |
1.44e1 |
SMART |
IQ
|
1453 |
1475 |
1.15e-1 |
SMART |
IQ
|
1476 |
1495 |
1.66e2 |
SMART |
IQ
|
1503 |
1525 |
1.65e-2 |
SMART |
IQ
|
1526 |
1548 |
1.32e1 |
SMART |
IQ
|
1549 |
1571 |
1.48e1 |
SMART |
IQ
|
1572 |
1594 |
2.5e1 |
SMART |
IQ
|
1599 |
1621 |
2.58e-4 |
SMART |
IQ
|
1622 |
1644 |
6.7e-3 |
SMART |
IQ
|
1645 |
1667 |
4.25e1 |
SMART |
IQ
|
1668 |
1694 |
1.03e2 |
SMART |
IQ
|
1695 |
1717 |
2.33e-2 |
SMART |
IQ
|
1718 |
1740 |
7.79e0 |
SMART |
IQ
|
1741 |
1763 |
1.57e2 |
SMART |
IQ
|
1768 |
1790 |
2.68e-2 |
SMART |
IQ
|
1791 |
1813 |
5.83e-3 |
SMART |
IQ
|
1814 |
1836 |
5.93e1 |
SMART |
IQ
|
1841 |
1863 |
1.92e-3 |
SMART |
IQ
|
1864 |
1886 |
3.79e-2 |
SMART |
IQ
|
1914 |
1936 |
4.11e0 |
SMART |
IQ
|
1937 |
1959 |
1.87e-1 |
SMART |
IQ
|
1960 |
1982 |
6.27e1 |
SMART |
IQ
|
1987 |
2009 |
8.25e-3 |
SMART |
IQ
|
2010 |
2032 |
5.73e0 |
SMART |
IQ
|
2060 |
2082 |
1.39e0 |
SMART |
IQ
|
2083 |
2105 |
4.62e1 |
SMART |
IQ
|
2133 |
2155 |
5.58e0 |
SMART |
IQ
|
2156 |
2178 |
7.07e-2 |
SMART |
IQ
|
2206 |
2228 |
1.18e-3 |
SMART |
IQ
|
2229 |
2251 |
4.59e0 |
SMART |
IQ
|
2278 |
2300 |
1.85e-5 |
SMART |
IQ
|
2301 |
2323 |
8.13e-2 |
SMART |
IQ
|
2342 |
2364 |
9.62e-4 |
SMART |
IQ
|
2365 |
2387 |
4.12e-3 |
SMART |
IQ
|
2415 |
2437 |
7.58e-2 |
SMART |
IQ
|
2438 |
2460 |
2.6e0 |
SMART |
IQ
|
2490 |
2512 |
1.68e-3 |
SMART |
IQ
|
2513 |
2535 |
8.51e1 |
SMART |
IQ
|
2560 |
2582 |
2.14e-1 |
SMART |
IQ
|
2601 |
2623 |
8.46e0 |
SMART |
IQ
|
2647 |
2669 |
1.15e1 |
SMART |
IQ
|
2673 |
2695 |
1.95e-4 |
SMART |
IQ
|
2696 |
2718 |
4.13e1 |
SMART |
IQ
|
2723 |
2745 |
1.02e-2 |
SMART |
IQ
|
2761 |
2783 |
3.14e2 |
SMART |
IQ
|
2784 |
2806 |
1e1 |
SMART |
IQ
|
2825 |
2847 |
2.43e0 |
SMART |
IQ
|
2848 |
2870 |
4.6e-1 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000196272
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000199998
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000200083
|
SMART Domains |
Protein: ENSMUSP00000142880 Gene: ENSMUSG00000033952
Domain | Start | End | E-Value | Type |
low complexity region
|
855 |
861 |
N/A |
INTRINSIC |
CH
|
890 |
1022 |
2.04e0 |
SMART |
CH
|
1080 |
1224 |
5.56e-9 |
SMART |
IQ
|
1233 |
1255 |
7.57e0 |
SMART |
IQ
|
1259 |
1281 |
1.12e1 |
SMART |
IQ
|
1282 |
1304 |
3.73e-1 |
SMART |
IQ
|
1314 |
1336 |
1.25e1 |
SMART |
IQ
|
1337 |
1358 |
2.96e1 |
SMART |
IQ
|
1382 |
1404 |
1.15e1 |
SMART |
IQ
|
1408 |
1430 |
1.95e-4 |
SMART |
IQ
|
1431 |
1453 |
4.13e1 |
SMART |
IQ
|
1458 |
1480 |
1.02e-2 |
SMART |
IQ
|
1496 |
1518 |
3.14e2 |
SMART |
IQ
|
1519 |
1541 |
1e1 |
SMART |
IQ
|
1560 |
1582 |
2.43e0 |
SMART |
IQ
|
1583 |
1605 |
4.6e-1 |
SMART |
|
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 is the human ortholog of the Drosophila melanogaster 'abnormal spindle' gene (asp), which is essential for normal mitotic spindle function in embryonic neuroblasts. Studies in mouse also suggest a role of this gene in mitotic spindle regulation, with a preferential role in regulating neurogenesis. Mutations in this gene are associated with microcephaly primary type 5. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011] PHENOTYPE: Mice homozygous for protein-truncating gene trap mutations of this gene exhibit decreased body weight, microcephaly, a severe reduction in brain, testis and ovary weight, oligozoospermia and asthenospermia, and reduced fertility in both sexes. [provided by MGI curators]
|
Allele List at MGI |
All alleles(9) : Targeted, other(2) Gene trapped(7) |
Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg6 |
T |
C |
10: 14,440,403 |
|
probably null |
Het |
Alcam |
T |
A |
16: 52,295,017 |
|
probably benign |
Het |
Bag6 |
T |
A |
17: 35,144,651 |
D770E |
probably damaging |
Het |
Baz2b |
A |
T |
2: 59,957,675 |
Y724* |
probably null |
Het |
Ccdc178 |
A |
T |
18: 21,844,911 |
I833N |
probably benign |
Het |
Ccdc28a |
C |
A |
10: 18,230,513 |
V22F |
possibly damaging |
Het |
Cmya5 |
T |
C |
13: 93,093,120 |
N1820S |
probably benign |
Het |
Fancm |
T |
G |
12: 65,106,193 |
I1141S |
probably benign |
Het |
Fgfrl1 |
G |
A |
5: 108,705,887 |
G287S |
probably damaging |
Het |
Galntl6 |
G |
A |
8: 57,857,540 |
P376S |
probably damaging |
Het |
Gm21985 |
A |
G |
2: 112,337,997 |
|
probably benign |
Het |
Hck |
A |
G |
2: 153,151,019 |
E482G |
possibly damaging |
Het |
Kcna3 |
C |
T |
3: 107,037,156 |
S245L |
probably benign |
Het |
Mcc |
T |
C |
18: 44,449,216 |
M798V |
possibly damaging |
Het |
Nlrp9c |
T |
C |
7: 26,384,588 |
Y522C |
probably benign |
Het |
Ofcc1 |
C |
A |
13: 40,280,491 |
S46I |
probably damaging |
Het |
Pdgfra |
A |
G |
5: 75,163,679 |
D65G |
probably benign |
Het |
Phf24 |
A |
C |
4: 42,933,905 |
T59P |
possibly damaging |
Het |
Pik3cg |
A |
G |
12: 32,205,149 |
Y280H |
probably damaging |
Het |
Pkd1l1 |
C |
A |
11: 8,834,773 |
|
probably null |
Het |
Plcd4 |
C |
A |
1: 74,552,115 |
T223N |
probably damaging |
Het |
Polr1b |
G |
A |
2: 129,125,909 |
G1074D |
probably damaging |
Het |
Pou2f3 |
T |
C |
9: 43,128,893 |
T367A |
probably damaging |
Het |
Prkdc |
T |
A |
16: 15,799,926 |
M3207K |
possibly damaging |
Het |
Rb1cc1 |
T |
C |
1: 6,249,506 |
S1050P |
probably damaging |
Het |
Sf3b3 |
G |
A |
8: 110,813,751 |
R1013* |
probably null |
Het |
Svep1 |
T |
C |
4: 58,068,988 |
T2933A |
possibly damaging |
Het |
Vwf |
A |
G |
6: 125,658,872 |
R289G |
unknown |
Het |
Zfp263 |
T |
C |
16: 3,745,846 |
S155P |
probably benign |
Het |
|
Other mutations in Aspm |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00594:Aspm
|
APN |
1 |
139487422 |
splice site |
probably benign |
|
IGL00808:Aspm
|
APN |
1 |
139461476 |
missense |
probably benign |
0.03 |
IGL00897:Aspm
|
APN |
1 |
139477407 |
missense |
probably damaging |
0.98 |
IGL01024:Aspm
|
APN |
1 |
139478124 |
missense |
possibly damaging |
0.66 |
IGL01410:Aspm
|
APN |
1 |
139482444 |
missense |
probably benign |
0.25 |
IGL01588:Aspm
|
APN |
1 |
139478162 |
missense |
probably benign |
0.11 |
IGL01610:Aspm
|
APN |
1 |
139489670 |
nonsense |
probably null |
|
IGL01633:Aspm
|
APN |
1 |
139480836 |
missense |
possibly damaging |
0.93 |
IGL01982:Aspm
|
APN |
1 |
139491588 |
missense |
probably benign |
0.12 |
IGL02429:Aspm
|
APN |
1 |
139479810 |
missense |
probably benign |
0.27 |
IGL02468:Aspm
|
APN |
1 |
139480950 |
missense |
probably damaging |
1.00 |
IGL02519:Aspm
|
APN |
1 |
139461927 |
splice site |
probably benign |
|
IGL02526:Aspm
|
APN |
1 |
139489719 |
missense |
probably benign |
0.03 |
IGL02716:Aspm
|
APN |
1 |
139479687 |
missense |
probably damaging |
1.00 |
IGL02876:Aspm
|
APN |
1 |
139473653 |
missense |
probably damaging |
1.00 |
IGL02953:Aspm
|
APN |
1 |
139457419 |
missense |
probably benign |
0.01 |
IGL03275:Aspm
|
APN |
1 |
139487295 |
missense |
probably damaging |
1.00 |
Stemware
|
UTSW |
1 |
139477459 |
nonsense |
probably null |
|
3-1:Aspm
|
UTSW |
1 |
139457541 |
missense |
probably benign |
|
R0016:Aspm
|
UTSW |
1 |
139479544 |
missense |
probably benign |
0.01 |
R0016:Aspm
|
UTSW |
1 |
139479544 |
missense |
probably benign |
0.01 |
R0106:Aspm
|
UTSW |
1 |
139476876 |
missense |
probably benign |
0.02 |
R0106:Aspm
|
UTSW |
1 |
139476876 |
missense |
probably benign |
0.02 |
R0140:Aspm
|
UTSW |
1 |
139480641 |
missense |
probably benign |
0.00 |
R0195:Aspm
|
UTSW |
1 |
139479135 |
missense |
probably damaging |
1.00 |
R0217:Aspm
|
UTSW |
1 |
139457880 |
missense |
possibly damaging |
0.46 |
R0276:Aspm
|
UTSW |
1 |
139478471 |
missense |
possibly damaging |
0.95 |
R0309:Aspm
|
UTSW |
1 |
139482511 |
splice site |
probably benign |
|
R0466:Aspm
|
UTSW |
1 |
139477901 |
missense |
probably damaging |
1.00 |
R0520:Aspm
|
UTSW |
1 |
139478820 |
missense |
possibly damaging |
0.51 |
R0615:Aspm
|
UTSW |
1 |
139487289 |
missense |
probably damaging |
1.00 |
R0626:Aspm
|
UTSW |
1 |
139491601 |
missense |
probably damaging |
1.00 |
R0660:Aspm
|
UTSW |
1 |
139457764 |
missense |
probably benign |
0.03 |
R0751:Aspm
|
UTSW |
1 |
139456898 |
splice site |
probably benign |
|
R0830:Aspm
|
UTSW |
1 |
139474254 |
missense |
probably damaging |
0.99 |
R1109:Aspm
|
UTSW |
1 |
139456758 |
missense |
probably damaging |
0.99 |
R1114:Aspm
|
UTSW |
1 |
139461924 |
splice site |
probably benign |
|
R1130:Aspm
|
UTSW |
1 |
139477834 |
missense |
possibly damaging |
0.90 |
R1298:Aspm
|
UTSW |
1 |
139457419 |
missense |
probably benign |
0.01 |
R1386:Aspm
|
UTSW |
1 |
139457623 |
missense |
probably benign |
0.03 |
R1386:Aspm
|
UTSW |
1 |
139478972 |
missense |
possibly damaging |
0.80 |
R1557:Aspm
|
UTSW |
1 |
139468668 |
missense |
probably benign |
0.01 |
R1625:Aspm
|
UTSW |
1 |
139481039 |
missense |
probably benign |
0.01 |
R1728:Aspm
|
UTSW |
1 |
139473574 |
missense |
probably benign |
|
R1729:Aspm
|
UTSW |
1 |
139473574 |
missense |
probably benign |
|
R1730:Aspm
|
UTSW |
1 |
139473574 |
missense |
probably benign |
|
R1733:Aspm
|
UTSW |
1 |
139457117 |
missense |
probably benign |
0.27 |
R1739:Aspm
|
UTSW |
1 |
139473574 |
missense |
probably benign |
|
R1762:Aspm
|
UTSW |
1 |
139473574 |
missense |
probably benign |
|
R1783:Aspm
|
UTSW |
1 |
139473574 |
missense |
probably benign |
|
R1784:Aspm
|
UTSW |
1 |
139473574 |
missense |
probably benign |
|
R1785:Aspm
|
UTSW |
1 |
139473574 |
missense |
probably benign |
|
R1793:Aspm
|
UTSW |
1 |
139457341 |
missense |
probably benign |
0.00 |
R1893:Aspm
|
UTSW |
1 |
139479867 |
missense |
probably damaging |
1.00 |
R1911:Aspm
|
UTSW |
1 |
139478094 |
missense |
probably benign |
0.06 |
R2103:Aspm
|
UTSW |
1 |
139491665 |
missense |
probably damaging |
0.99 |
R2128:Aspm
|
UTSW |
1 |
139457635 |
missense |
probably benign |
0.14 |
R2129:Aspm
|
UTSW |
1 |
139457635 |
missense |
probably benign |
0.14 |
R2239:Aspm
|
UTSW |
1 |
139456846 |
missense |
possibly damaging |
0.67 |
R2352:Aspm
|
UTSW |
1 |
139457562 |
missense |
probably benign |
0.02 |
R2353:Aspm
|
UTSW |
1 |
139477697 |
missense |
probably damaging |
1.00 |
R2380:Aspm
|
UTSW |
1 |
139479348 |
missense |
probably damaging |
1.00 |
R2413:Aspm
|
UTSW |
1 |
139477757 |
missense |
probably damaging |
1.00 |
R2421:Aspm
|
UTSW |
1 |
139488487 |
missense |
possibly damaging |
0.49 |
R3607:Aspm
|
UTSW |
1 |
139480668 |
missense |
probably benign |
0.13 |
R3711:Aspm
|
UTSW |
1 |
139458100 |
missense |
probably benign |
0.17 |
R3718:Aspm
|
UTSW |
1 |
139480889 |
missense |
probably benign |
0.09 |
R3718:Aspm
|
UTSW |
1 |
139490427 |
missense |
probably benign |
0.31 |
R3741:Aspm
|
UTSW |
1 |
139478619 |
missense |
possibly damaging |
0.47 |
R3788:Aspm
|
UTSW |
1 |
139463203 |
missense |
probably damaging |
1.00 |
R3838:Aspm
|
UTSW |
1 |
139478054 |
missense |
probably benign |
0.24 |
R3839:Aspm
|
UTSW |
1 |
139478054 |
missense |
probably benign |
0.24 |
R3849:Aspm
|
UTSW |
1 |
139458286 |
missense |
probably benign |
0.21 |
R4075:Aspm
|
UTSW |
1 |
139474285 |
missense |
probably damaging |
1.00 |
R4080:Aspm
|
UTSW |
1 |
139470755 |
missense |
probably damaging |
1.00 |
R4463:Aspm
|
UTSW |
1 |
139455010 |
missense |
possibly damaging |
0.95 |
R4537:Aspm
|
UTSW |
1 |
139474303 |
missense |
probably benign |
0.01 |
R4547:Aspm
|
UTSW |
1 |
139478187 |
missense |
possibly damaging |
0.75 |
R4573:Aspm
|
UTSW |
1 |
139479507 |
missense |
probably damaging |
0.98 |
R4680:Aspm
|
UTSW |
1 |
139480671 |
missense |
probably benign |
0.05 |
R4807:Aspm
|
UTSW |
1 |
139477919 |
missense |
probably damaging |
1.00 |
R4840:Aspm
|
UTSW |
1 |
139470531 |
missense |
possibly damaging |
0.83 |
R4854:Aspm
|
UTSW |
1 |
139478072 |
nonsense |
probably null |
|
R4859:Aspm
|
UTSW |
1 |
139469393 |
missense |
probably damaging |
1.00 |
R4893:Aspm
|
UTSW |
1 |
139489839 |
critical splice donor site |
probably null |
|
R4910:Aspm
|
UTSW |
1 |
139491543 |
missense |
probably damaging |
1.00 |
R4953:Aspm
|
UTSW |
1 |
139471734 |
missense |
probably benign |
0.00 |
R4974:Aspm
|
UTSW |
1 |
139478010 |
missense |
probably benign |
0.03 |
R4981:Aspm
|
UTSW |
1 |
139470760 |
splice site |
probably null |
|
R5082:Aspm
|
UTSW |
1 |
139478676 |
nonsense |
probably null |
|
R5223:Aspm
|
UTSW |
1 |
139478334 |
missense |
probably damaging |
1.00 |
R5268:Aspm
|
UTSW |
1 |
139464295 |
missense |
probably damaging |
1.00 |
R5371:Aspm
|
UTSW |
1 |
139470541 |
nonsense |
probably null |
|
R5377:Aspm
|
UTSW |
1 |
139457483 |
missense |
probably damaging |
0.96 |
R5377:Aspm
|
UTSW |
1 |
139470395 |
splice site |
probably null |
|
R5481:Aspm
|
UTSW |
1 |
139457061 |
missense |
possibly damaging |
0.85 |
R5513:Aspm
|
UTSW |
1 |
139482398 |
missense |
probably damaging |
1.00 |
R5578:Aspm
|
UTSW |
1 |
139470717 |
missense |
probably damaging |
1.00 |
R5649:Aspm
|
UTSW |
1 |
139479669 |
missense |
probably benign |
|
R5685:Aspm
|
UTSW |
1 |
139487288 |
missense |
probably benign |
0.10 |
R5695:Aspm
|
UTSW |
1 |
139479669 |
missense |
probably benign |
|
R5766:Aspm
|
UTSW |
1 |
139479002 |
missense |
probably damaging |
0.99 |
R5964:Aspm
|
UTSW |
1 |
139455227 |
intron |
probably benign |
|
R5993:Aspm
|
UTSW |
1 |
139479531 |
missense |
probably benign |
0.28 |
R6027:Aspm
|
UTSW |
1 |
139463056 |
missense |
probably damaging |
1.00 |
R6029:Aspm
|
UTSW |
1 |
139480990 |
missense |
possibly damaging |
0.83 |
R6102:Aspm
|
UTSW |
1 |
139477459 |
nonsense |
probably null |
|
R6188:Aspm
|
UTSW |
1 |
139479239 |
missense |
possibly damaging |
0.79 |
R6257:Aspm
|
UTSW |
1 |
139482053 |
splice site |
probably null |
|
R6433:Aspm
|
UTSW |
1 |
139473683 |
missense |
probably damaging |
1.00 |
R6682:Aspm
|
UTSW |
1 |
139457722 |
missense |
possibly damaging |
0.67 |
R6763:Aspm
|
UTSW |
1 |
139470517 |
missense |
possibly damaging |
0.64 |
R6798:Aspm
|
UTSW |
1 |
139468685 |
missense |
possibly damaging |
0.66 |
R6815:Aspm
|
UTSW |
1 |
139480142 |
missense |
probably benign |
0.04 |
R6854:Aspm
|
UTSW |
1 |
139463182 |
missense |
possibly damaging |
0.90 |
R6928:Aspm
|
UTSW |
1 |
139480206 |
nonsense |
probably null |
|
R6943:Aspm
|
UTSW |
1 |
139480542 |
missense |
probably damaging |
1.00 |
R6979:Aspm
|
UTSW |
1 |
139480485 |
missense |
probably damaging |
1.00 |
R6998:Aspm
|
UTSW |
1 |
139469472 |
missense |
probably damaging |
1.00 |
R7126:Aspm
|
UTSW |
1 |
139480803 |
missense |
probably benign |
0.27 |
R7237:Aspm
|
UTSW |
1 |
139477929 |
missense |
possibly damaging |
0.81 |
R7240:Aspm
|
UTSW |
1 |
139478651 |
nonsense |
probably null |
|
R7272:Aspm
|
UTSW |
1 |
139458328 |
missense |
probably benign |
0.14 |
R7427:Aspm
|
UTSW |
1 |
139457616 |
missense |
probably benign |
0.01 |
R7519:Aspm
|
UTSW |
1 |
139490336 |
missense |
possibly damaging |
0.53 |
R7776:Aspm
|
UTSW |
1 |
139479846 |
missense |
possibly damaging |
0.85 |
R7875:Aspm
|
UTSW |
1 |
139455134 |
missense |
probably benign |
0.02 |
R7883:Aspm
|
UTSW |
1 |
139478667 |
missense |
possibly damaging |
0.47 |
R7964:Aspm
|
UTSW |
1 |
139480686 |
missense |
probably damaging |
1.00 |
R8012:Aspm
|
UTSW |
1 |
139457464 |
missense |
probably benign |
0.03 |
R8029:Aspm
|
UTSW |
1 |
139471632 |
missense |
probably benign |
0.00 |
R8233:Aspm
|
UTSW |
1 |
139457304 |
missense |
probably benign |
0.28 |
R8277:Aspm
|
UTSW |
1 |
139455010 |
missense |
probably damaging |
1.00 |
R8345:Aspm
|
UTSW |
1 |
139464273 |
nonsense |
probably null |
|
R8491:Aspm
|
UTSW |
1 |
139457695 |
missense |
probably damaging |
0.98 |
R8511:Aspm
|
UTSW |
1 |
139457308 |
missense |
probably damaging |
1.00 |
R8557:Aspm
|
UTSW |
1 |
139456756 |
missense |
probably benign |
0.01 |
R8927:Aspm
|
UTSW |
1 |
139490387 |
nonsense |
probably null |
|
R8928:Aspm
|
UTSW |
1 |
139490387 |
nonsense |
probably null |
|
R8950:Aspm
|
UTSW |
1 |
139478952 |
missense |
probably damaging |
1.00 |
R9033:Aspm
|
UTSW |
1 |
139478127 |
missense |
probably damaging |
1.00 |
R9083:Aspm
|
UTSW |
1 |
139493698 |
missense |
possibly damaging |
0.70 |
R9133:Aspm
|
UTSW |
1 |
139491528 |
missense |
probably damaging |
1.00 |
R9160:Aspm
|
UTSW |
1 |
139490124 |
missense |
probably damaging |
1.00 |
R9179:Aspm
|
UTSW |
1 |
139476715 |
missense |
probably damaging |
1.00 |
R9265:Aspm
|
UTSW |
1 |
139461444 |
missense |
probably benign |
0.24 |
R9400:Aspm
|
UTSW |
1 |
139479903 |
missense |
probably damaging |
1.00 |
R9419:Aspm
|
UTSW |
1 |
139457185 |
missense |
probably benign |
0.29 |
R9454:Aspm
|
UTSW |
1 |
139480994 |
missense |
probably benign |
0.00 |
X0063:Aspm
|
UTSW |
1 |
139458090 |
missense |
probably benign |
0.01 |
|
Posted On |
2012-12-06 |