Incidental Mutation 'IGL01530:Acin1'
ID |
89714 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Acin1
|
Ensembl Gene |
ENSMUSG00000022185 |
Gene Name |
apoptotic chromatin condensation inducer 1 |
Synonyms |
2610036I19Rik, 2610510L13Rik, Acinus |
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.940)
|
Stock # |
IGL01530
|
Quality Score |
|
Status
|
|
Chromosome |
14 |
Chromosomal Location |
54879618-54924388 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 54881443 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Tryptophan
at position 1117
(R1117W)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022793]
[ENSMUST00000022794]
[ENSMUST00000067784]
[ENSMUST00000111484]
[ENSMUST00000123875]
[ENSMUST00000169818]
[ENSMUST00000150371]
[ENSMUST00000141453]
[ENSMUST00000167015]
[ENSMUST00000148754]
[ENSMUST00000126166]
|
AlphaFold |
Q9JIX8 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000022793
AA Change: R1184W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000022793 Gene: ENSMUSG00000022185 AA Change: R1184W
Domain | Start | End | E-Value | Type |
SAP
|
72 |
106 |
1.29e-8 |
SMART |
coiled coil region
|
138 |
175 |
N/A |
INTRINSIC |
low complexity region
|
205 |
220 |
N/A |
INTRINSIC |
coiled coil region
|
259 |
300 |
N/A |
INTRINSIC |
low complexity region
|
378 |
396 |
N/A |
INTRINSIC |
low complexity region
|
414 |
423 |
N/A |
INTRINSIC |
low complexity region
|
573 |
603 |
N/A |
INTRINSIC |
low complexity region
|
631 |
662 |
N/A |
INTRINSIC |
low complexity region
|
734 |
743 |
N/A |
INTRINSIC |
low complexity region
|
760 |
773 |
N/A |
INTRINSIC |
low complexity region
|
778 |
792 |
N/A |
INTRINSIC |
low complexity region
|
803 |
813 |
N/A |
INTRINSIC |
internal_repeat_1
|
817 |
892 |
1.63e-6 |
PROSPERO |
low complexity region
|
927 |
952 |
N/A |
INTRINSIC |
RRM
|
1012 |
1081 |
8.3e-2 |
SMART |
Pfam:RSB_motif
|
1139 |
1246 |
5.7e-30 |
PFAM |
low complexity region
|
1275 |
1329 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000022794
AA Change: R426W
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000022794 Gene: ENSMUSG00000022185 AA Change: R426W
Domain | Start | End | E-Value | Type |
low complexity region
|
21 |
35 |
N/A |
INTRINSIC |
low complexity region
|
46 |
56 |
N/A |
INTRINSIC |
low complexity region
|
169 |
194 |
N/A |
INTRINSIC |
RRM
|
254 |
323 |
8.3e-2 |
SMART |
low complexity region
|
355 |
405 |
N/A |
INTRINSIC |
low complexity region
|
412 |
450 |
N/A |
INTRINSIC |
PDB:4A8X|B
|
451 |
475 |
4e-6 |
PDB |
low complexity region
|
477 |
512 |
N/A |
INTRINSIC |
low complexity region
|
517 |
571 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000067784
|
SMART Domains |
Protein: ENSMUSP00000066005 Gene: ENSMUSG00000059674
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
CA
|
67 |
148 |
7.85e-18 |
SMART |
CA
|
172 |
257 |
3.23e-28 |
SMART |
CA
|
281 |
369 |
4.24e-14 |
SMART |
CA
|
396 |
477 |
1.48e-22 |
SMART |
Blast:CA
|
500 |
581 |
3e-31 |
BLAST |
transmembrane domain
|
602 |
624 |
N/A |
INTRINSIC |
Pfam:Cadherin_C
|
627 |
775 |
2e-48 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000111484
AA Change: R1144W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000107109 Gene: ENSMUSG00000022185 AA Change: R1144W
Domain | Start | End | E-Value | Type |
SAP
|
72 |
106 |
1.29e-8 |
SMART |
coiled coil region
|
138 |
172 |
N/A |
INTRINSIC |
coiled coil region
|
219 |
260 |
N/A |
INTRINSIC |
low complexity region
|
338 |
356 |
N/A |
INTRINSIC |
low complexity region
|
374 |
383 |
N/A |
INTRINSIC |
low complexity region
|
533 |
563 |
N/A |
INTRINSIC |
low complexity region
|
591 |
622 |
N/A |
INTRINSIC |
low complexity region
|
694 |
703 |
N/A |
INTRINSIC |
low complexity region
|
720 |
733 |
N/A |
INTRINSIC |
low complexity region
|
738 |
752 |
N/A |
INTRINSIC |
low complexity region
|
763 |
773 |
N/A |
INTRINSIC |
internal_repeat_1
|
777 |
852 |
1.21e-6 |
PROSPERO |
low complexity region
|
887 |
912 |
N/A |
INTRINSIC |
RRM
|
972 |
1041 |
8.3e-2 |
SMART |
low complexity region
|
1073 |
1123 |
N/A |
INTRINSIC |
low complexity region
|
1130 |
1168 |
N/A |
INTRINSIC |
coiled coil region
|
1188 |
1253 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000123875
|
SMART Domains |
Protein: ENSMUSP00000117210 Gene: ENSMUSG00000022185
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
35 |
N/A |
INTRINSIC |
low complexity region
|
87 |
101 |
N/A |
INTRINSIC |
low complexity region
|
112 |
122 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000124271
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000125767
|
Predicted Effect |
unknown
Transcript: ENSMUST00000169818
AA Change: R43Q
|
SMART Domains |
Protein: ENSMUSP00000131860 Gene: ENSMUSG00000091306 AA Change: R43Q
Domain | Start | End | E-Value | Type |
low complexity region
|
1 |
61 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000150371
AA Change: R480W
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000118069 Gene: ENSMUSG00000022185 AA Change: R480W
Domain | Start | End | E-Value | Type |
low complexity region
|
19 |
35 |
N/A |
INTRINSIC |
low complexity region
|
74 |
88 |
N/A |
INTRINSIC |
low complexity region
|
99 |
109 |
N/A |
INTRINSIC |
low complexity region
|
223 |
248 |
N/A |
INTRINSIC |
RRM
|
308 |
377 |
8.3e-2 |
SMART |
low complexity region
|
409 |
459 |
N/A |
INTRINSIC |
low complexity region
|
466 |
504 |
N/A |
INTRINSIC |
PDB:4A8X|B
|
505 |
529 |
3e-6 |
PDB |
low complexity region
|
531 |
566 |
N/A |
INTRINSIC |
low complexity region
|
571 |
625 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000141453
AA Change: R398W
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000116664 Gene: ENSMUSG00000022185 AA Change: R398W
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
19 |
N/A |
INTRINSIC |
low complexity region
|
30 |
40 |
N/A |
INTRINSIC |
low complexity region
|
141 |
166 |
N/A |
INTRINSIC |
RRM
|
226 |
295 |
8.3e-2 |
SMART |
low complexity region
|
327 |
377 |
N/A |
INTRINSIC |
low complexity region
|
384 |
422 |
N/A |
INTRINSIC |
PDB:4A8X|B
|
423 |
447 |
4e-6 |
PDB |
low complexity region
|
449 |
484 |
N/A |
INTRINSIC |
low complexity region
|
489 |
543 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000152773
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000147714
AA Change: R1117W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000119080 Gene: ENSMUSG00000022185 AA Change: R1117W
Domain | Start | End | E-Value | Type |
SAP
|
18 |
52 |
1.29e-8 |
SMART |
coiled coil region
|
83 |
120 |
N/A |
INTRINSIC |
low complexity region
|
151 |
166 |
N/A |
INTRINSIC |
coiled coil region
|
204 |
245 |
N/A |
INTRINSIC |
low complexity region
|
324 |
342 |
N/A |
INTRINSIC |
low complexity region
|
360 |
369 |
N/A |
INTRINSIC |
low complexity region
|
519 |
549 |
N/A |
INTRINSIC |
low complexity region
|
577 |
608 |
N/A |
INTRINSIC |
low complexity region
|
680 |
689 |
N/A |
INTRINSIC |
low complexity region
|
706 |
719 |
N/A |
INTRINSIC |
low complexity region
|
724 |
738 |
N/A |
INTRINSIC |
low complexity region
|
749 |
759 |
N/A |
INTRINSIC |
low complexity region
|
861 |
886 |
N/A |
INTRINSIC |
RRM
|
946 |
1015 |
8.3e-2 |
SMART |
Pfam:RSB_motif
|
1065 |
1180 |
1.1e-29 |
PFAM |
low complexity region
|
1209 |
1263 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000138321
AA Change: R75W
|
SMART Domains |
Protein: ENSMUSP00000119326 Gene: ENSMUSG00000022185 AA Change: R75W
Domain | Start | End | E-Value | Type |
Pfam:RSB_motif
|
20 |
128 |
4.7e-23 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000167015
AA Change: R427W
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000125776 Gene: ENSMUSG00000022185 AA Change: R427W
Domain | Start | End | E-Value | Type |
low complexity region
|
21 |
35 |
N/A |
INTRINSIC |
low complexity region
|
46 |
56 |
N/A |
INTRINSIC |
low complexity region
|
170 |
195 |
N/A |
INTRINSIC |
RRM
|
255 |
324 |
8.3e-2 |
SMART |
low complexity region
|
356 |
406 |
N/A |
INTRINSIC |
low complexity region
|
413 |
451 |
N/A |
INTRINSIC |
PDB:4A8X|B
|
452 |
476 |
4e-6 |
PDB |
low complexity region
|
478 |
513 |
N/A |
INTRINSIC |
low complexity region
|
518 |
572 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000148754
AA Change: R427W
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000122003 Gene: ENSMUSG00000022185 AA Change: R427W
Domain | Start | End | E-Value | Type |
low complexity region
|
21 |
35 |
N/A |
INTRINSIC |
low complexity region
|
46 |
56 |
N/A |
INTRINSIC |
low complexity region
|
170 |
195 |
N/A |
INTRINSIC |
RRM
|
255 |
324 |
8.3e-2 |
SMART |
low complexity region
|
356 |
406 |
N/A |
INTRINSIC |
low complexity region
|
413 |
451 |
N/A |
INTRINSIC |
PDB:4A8X|B
|
452 |
476 |
4e-6 |
PDB |
low complexity region
|
478 |
513 |
N/A |
INTRINSIC |
low complexity region
|
518 |
572 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000126166
AA Change: R411W
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000114546 Gene: ENSMUSG00000022185 AA Change: R411W
Domain | Start | End | E-Value | Type |
low complexity region
|
5 |
19 |
N/A |
INTRINSIC |
low complexity region
|
30 |
40 |
N/A |
INTRINSIC |
low complexity region
|
154 |
179 |
N/A |
INTRINSIC |
RRM
|
239 |
308 |
8.3e-2 |
SMART |
low complexity region
|
340 |
390 |
N/A |
INTRINSIC |
low complexity region
|
397 |
435 |
N/A |
INTRINSIC |
PDB:4A8X|B
|
436 |
460 |
4e-6 |
PDB |
low complexity region
|
462 |
497 |
N/A |
INTRINSIC |
low complexity region
|
502 |
556 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000196776
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000133706
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000170299
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000151487
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000167495
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Apoptosis is defined by several morphologic nuclear changes, including chromatin condensation and nuclear fragmentation. This gene encodes a nuclear protein that induces apoptotic chromatin condensation after activation by caspase-3, without inducing DNA fragmentation. This protein has also been shown to be a component of a splicing-dependent multiprotein exon junction complex (EJC) that is deposited at splice junctions on mRNAs, as a consequence of pre-mRNA splicing. It may thus be involved in mRNA metabolism associated with splicing. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acox2 |
T |
G |
14: 8,246,363 (GRCm38) |
Y476S |
probably damaging |
Het |
Arl6ip5 |
G |
A |
6: 97,187,785 (GRCm39) |
D2N |
possibly damaging |
Het |
Ces2h |
A |
G |
8: 105,741,116 (GRCm39) |
H36R |
probably benign |
Het |
Cfap44 |
C |
A |
16: 44,269,530 (GRCm39) |
A1178E |
probably damaging |
Het |
Clmn |
T |
A |
12: 104,758,115 (GRCm39) |
I134F |
probably damaging |
Het |
Col6a5 |
A |
G |
9: 105,792,385 (GRCm39) |
|
probably benign |
Het |
Csmd1 |
C |
T |
8: 15,953,195 (GRCm39) |
E3429K |
probably damaging |
Het |
Csmd2 |
A |
G |
4: 128,308,094 (GRCm39) |
D1284G |
possibly damaging |
Het |
Csmd3 |
C |
T |
15: 47,701,833 (GRCm39) |
G1750E |
possibly damaging |
Het |
Csmd3 |
T |
G |
15: 47,533,013 (GRCm39) |
D2516A |
probably damaging |
Het |
Depdc1a |
C |
T |
3: 159,229,560 (GRCm39) |
H631Y |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,174,213 (GRCm39) |
S2167T |
probably benign |
Het |
Flii |
G |
A |
11: 60,611,008 (GRCm39) |
R474* |
probably null |
Het |
Hmcn2 |
A |
C |
2: 31,244,276 (GRCm39) |
D687A |
possibly damaging |
Het |
Hrh4 |
A |
G |
18: 13,149,004 (GRCm39) |
|
probably benign |
Het |
Hsd3b5 |
G |
A |
3: 98,526,439 (GRCm39) |
R336C |
probably damaging |
Het |
Igkv5-39 |
T |
A |
6: 69,877,459 (GRCm39) |
E79V |
probably damaging |
Het |
Iqgap3 |
G |
A |
3: 88,019,610 (GRCm39) |
|
probably null |
Het |
Irak3 |
G |
A |
10: 119,978,699 (GRCm39) |
S492F |
probably benign |
Het |
Kif14 |
T |
A |
1: 136,406,157 (GRCm39) |
|
probably benign |
Het |
Kmt2c |
T |
C |
5: 25,518,498 (GRCm39) |
I2394V |
probably benign |
Het |
Lama1 |
C |
T |
17: 68,103,785 (GRCm39) |
A2002V |
probably benign |
Het |
Map3k19 |
T |
C |
1: 127,749,841 (GRCm39) |
E1170G |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,711,938 (GRCm39) |
|
probably benign |
Het |
Mpo |
G |
T |
11: 87,692,017 (GRCm39) |
M483I |
probably benign |
Het |
Neu3 |
T |
C |
7: 99,462,953 (GRCm39) |
S257G |
probably benign |
Het |
Nhsl3 |
G |
A |
4: 129,116,589 (GRCm39) |
|
probably null |
Het |
Niban3 |
A |
T |
8: 72,056,561 (GRCm39) |
|
probably benign |
Het |
Nup214 |
A |
G |
2: 31,923,733 (GRCm39) |
T1421A |
probably benign |
Het |
Pbx1 |
T |
C |
1: 168,018,873 (GRCm39) |
N324S |
probably benign |
Het |
Pcbp2 |
T |
C |
15: 102,392,601 (GRCm39) |
S5P |
probably benign |
Het |
Pds5b |
A |
G |
5: 150,715,640 (GRCm39) |
I511V |
probably benign |
Het |
Pdzph1 |
C |
T |
17: 59,229,710 (GRCm39) |
D983N |
probably damaging |
Het |
Phldb2 |
A |
C |
16: 45,623,092 (GRCm39) |
D651E |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,629,643 (GRCm39) |
|
probably null |
Het |
Plxnb1 |
A |
G |
9: 108,939,473 (GRCm39) |
D1406G |
probably benign |
Het |
Rhebl1 |
T |
C |
15: 98,777,367 (GRCm39) |
D65G |
probably damaging |
Het |
Smpdl3a |
A |
G |
10: 57,683,989 (GRCm39) |
H249R |
probably damaging |
Het |
Sorbs1 |
T |
C |
19: 40,365,091 (GRCm39) |
T231A |
probably benign |
Het |
Tmem232 |
G |
A |
17: 65,563,543 (GRCm39) |
Q617* |
probably null |
Het |
Trim62 |
A |
G |
4: 128,778,252 (GRCm39) |
D97G |
probably benign |
Het |
Tsc2 |
T |
C |
17: 24,841,636 (GRCm39) |
T328A |
possibly damaging |
Het |
Ugt2b5 |
C |
T |
5: 87,285,104 (GRCm39) |
V278I |
probably benign |
Het |
Usp4 |
T |
C |
9: 108,240,099 (GRCm39) |
|
probably null |
Het |
Vdac3-ps1 |
C |
T |
13: 18,206,091 (GRCm39) |
|
noncoding transcript |
Het |
Wwc2 |
T |
A |
8: 48,316,974 (GRCm39) |
R706S |
unknown |
Het |
Xpot |
A |
C |
10: 121,447,433 (GRCm39) |
I114S |
probably damaging |
Het |
Zfp777 |
T |
A |
6: 48,020,918 (GRCm39) |
S279C |
probably damaging |
Het |
|
Other mutations in Acin1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00988:Acin1
|
APN |
14 |
54,884,257 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02396:Acin1
|
APN |
14 |
54,882,256 (GRCm39) |
intron |
probably benign |
|
IGL02967:Acin1
|
APN |
14 |
54,880,210 (GRCm39) |
missense |
possibly damaging |
0.80 |
Protuberant
|
UTSW |
14 |
54,882,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R0411:Acin1
|
UTSW |
14 |
54,884,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R0723:Acin1
|
UTSW |
14 |
54,902,908 (GRCm39) |
missense |
probably damaging |
0.98 |
R0755:Acin1
|
UTSW |
14 |
54,889,292 (GRCm39) |
start codon destroyed |
probably null |
0.93 |
R0784:Acin1
|
UTSW |
14 |
54,890,985 (GRCm39) |
unclassified |
probably benign |
|
R1600:Acin1
|
UTSW |
14 |
54,881,174 (GRCm39) |
intron |
probably benign |
|
R1682:Acin1
|
UTSW |
14 |
54,901,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Acin1
|
UTSW |
14 |
54,901,995 (GRCm39) |
missense |
probably benign |
0.01 |
R1756:Acin1
|
UTSW |
14 |
54,902,661 (GRCm39) |
missense |
probably benign |
0.30 |
R1867:Acin1
|
UTSW |
14 |
54,881,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R1997:Acin1
|
UTSW |
14 |
54,884,156 (GRCm39) |
splice site |
probably null |
|
R2067:Acin1
|
UTSW |
14 |
54,902,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R3947:Acin1
|
UTSW |
14 |
54,916,790 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4374:Acin1
|
UTSW |
14 |
54,891,351 (GRCm39) |
unclassified |
probably benign |
|
R4476:Acin1
|
UTSW |
14 |
54,882,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R4501:Acin1
|
UTSW |
14 |
54,924,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R4547:Acin1
|
UTSW |
14 |
54,883,124 (GRCm39) |
missense |
probably benign |
0.01 |
R4621:Acin1
|
UTSW |
14 |
54,890,900 (GRCm39) |
unclassified |
probably benign |
|
R4657:Acin1
|
UTSW |
14 |
54,880,504 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4680:Acin1
|
UTSW |
14 |
54,924,215 (GRCm39) |
missense |
probably benign |
0.00 |
R4696:Acin1
|
UTSW |
14 |
54,880,474 (GRCm39) |
intron |
probably benign |
|
R4806:Acin1
|
UTSW |
14 |
54,916,685 (GRCm39) |
splice site |
probably benign |
|
R4826:Acin1
|
UTSW |
14 |
54,902,074 (GRCm39) |
missense |
probably damaging |
0.97 |
R5096:Acin1
|
UTSW |
14 |
54,916,679 (GRCm39) |
intron |
probably benign |
|
R5153:Acin1
|
UTSW |
14 |
54,883,070 (GRCm39) |
missense |
probably benign |
0.25 |
R5223:Acin1
|
UTSW |
14 |
54,880,398 (GRCm39) |
frame shift |
probably null |
|
R5260:Acin1
|
UTSW |
14 |
54,880,279 (GRCm39) |
intron |
probably benign |
|
R5525:Acin1
|
UTSW |
14 |
54,901,848 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5575:Acin1
|
UTSW |
14 |
54,916,195 (GRCm39) |
splice site |
probably null |
|
R5902:Acin1
|
UTSW |
14 |
54,901,130 (GRCm39) |
missense |
probably benign |
0.01 |
R6211:Acin1
|
UTSW |
14 |
54,881,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:Acin1
|
UTSW |
14 |
54,882,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R6560:Acin1
|
UTSW |
14 |
54,916,290 (GRCm39) |
missense |
probably benign |
0.24 |
R6916:Acin1
|
UTSW |
14 |
54,902,873 (GRCm39) |
missense |
probably benign |
0.27 |
R7201:Acin1
|
UTSW |
14 |
54,902,356 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7833:Acin1
|
UTSW |
14 |
54,902,059 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8096:Acin1
|
UTSW |
14 |
54,882,726 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8167:Acin1
|
UTSW |
14 |
54,902,337 (GRCm39) |
missense |
probably benign |
0.01 |
R8421:Acin1
|
UTSW |
14 |
54,880,486 (GRCm39) |
missense |
unknown |
|
R8771:Acin1
|
UTSW |
14 |
54,880,496 (GRCm39) |
missense |
unknown |
|
R8862:Acin1
|
UTSW |
14 |
54,901,172 (GRCm39) |
missense |
probably benign |
0.00 |
R9645:Acin1
|
UTSW |
14 |
54,901,913 (GRCm39) |
missense |
probably benign |
0.16 |
R9755:Acin1
|
UTSW |
14 |
54,889,292 (GRCm39) |
missense |
probably damaging |
0.99 |
X0021:Acin1
|
UTSW |
14 |
54,904,558 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Acin1
|
UTSW |
14 |
54,880,207 (GRCm39) |
missense |
unknown |
|
|
Posted On |
2013-12-03 |