Other mutations in this stock |
Total: 121 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
A |
G |
8: 87,253,910 (GRCm39) |
I958T |
probably benign |
Het |
Abcg5 |
AATCATTTG |
AG |
17: 84,981,030 (GRCm39) |
|
probably null |
Het |
Acap2 |
A |
G |
16: 30,952,345 (GRCm39) |
|
probably null |
Het |
Adgrb1 |
T |
C |
15: 74,411,726 (GRCm39) |
|
probably benign |
Het |
Akap6 |
T |
A |
12: 52,985,258 (GRCm39) |
V897E |
probably damaging |
Het |
Als2 |
A |
T |
1: 59,254,328 (GRCm39) |
L343Q |
probably benign |
Het |
Arhgap5 |
A |
G |
12: 52,589,376 (GRCm39) |
I1275M |
probably damaging |
Het |
Arnt |
C |
T |
3: 95,355,704 (GRCm39) |
S16L |
possibly damaging |
Het |
Bglap3 |
C |
T |
3: 88,284,300 (GRCm39) |
|
probably benign |
Het |
Blnk |
T |
C |
19: 40,928,609 (GRCm39) |
|
probably benign |
Het |
C1qtnf4 |
T |
C |
2: 90,720,003 (GRCm39) |
M92T |
probably damaging |
Het |
Ccdc177 |
G |
A |
12: 80,805,486 (GRCm39) |
R263C |
unknown |
Het |
Ccdc83 |
T |
A |
7: 89,893,362 (GRCm39) |
S132C |
probably damaging |
Het |
Cdc7 |
A |
G |
5: 107,120,940 (GRCm39) |
|
probably benign |
Het |
Cgnl1 |
T |
A |
9: 71,632,817 (GRCm39) |
N178I |
probably benign |
Het |
Col27a1 |
C |
T |
4: 63,191,354 (GRCm39) |
|
probably benign |
Het |
Col5a1 |
A |
T |
2: 27,876,766 (GRCm39) |
M822L |
unknown |
Het |
Coro7 |
T |
C |
16: 4,451,620 (GRCm39) |
I451V |
probably benign |
Het |
Csmd3 |
T |
C |
15: 48,536,927 (GRCm39) |
T92A |
probably damaging |
Het |
Ddc |
A |
G |
11: 11,765,292 (GRCm39) |
V460A |
possibly damaging |
Het |
Ddx4 |
C |
T |
13: 112,736,547 (GRCm39) |
V608I |
probably damaging |
Het |
Ddx60 |
A |
T |
8: 62,425,240 (GRCm39) |
H676L |
possibly damaging |
Het |
Dmtf1 |
T |
C |
5: 9,198,989 (GRCm39) |
E48G |
probably benign |
Het |
Dpf3 |
T |
A |
12: 83,371,809 (GRCm39) |
|
probably null |
Het |
Dydc2 |
A |
G |
14: 40,783,860 (GRCm39) |
C88R |
probably benign |
Het |
Elovl4 |
A |
G |
9: 83,662,772 (GRCm39) |
Y163H |
probably damaging |
Het |
Enpp2 |
T |
C |
15: 54,746,378 (GRCm39) |
D296G |
probably damaging |
Het |
Fam83h |
G |
T |
15: 75,878,419 (GRCm39) |
|
probably benign |
Het |
Fbf1 |
T |
A |
11: 116,042,317 (GRCm39) |
Q511L |
possibly damaging |
Het |
Fhdc1 |
A |
T |
3: 84,362,158 (GRCm39) |
L323Q |
probably damaging |
Het |
Fmnl2 |
T |
A |
2: 52,995,588 (GRCm39) |
V437D |
possibly damaging |
Het |
Foxo3 |
A |
G |
10: 42,073,258 (GRCm39) |
S420P |
probably benign |
Het |
Foxp4 |
C |
T |
17: 48,186,796 (GRCm39) |
R378Q |
unknown |
Het |
Garem2 |
G |
T |
5: 30,322,172 (GRCm39) |
G844* |
probably null |
Het |
Glmp |
T |
C |
3: 88,235,177 (GRCm39) |
L269S |
probably damaging |
Het |
Gm9915 |
T |
C |
1: 42,269,881 (GRCm39) |
|
noncoding transcript |
Het |
Gnb4 |
A |
T |
3: 32,652,290 (GRCm39) |
D27E |
probably damaging |
Het |
Gnb5 |
A |
G |
9: 75,251,932 (GRCm39) |
|
probably null |
Het |
Gpr161 |
T |
G |
1: 165,133,927 (GRCm39) |
V63G |
probably damaging |
Het |
Gsk3a |
T |
A |
7: 24,929,146 (GRCm39) |
|
probably benign |
Het |
Hapln2 |
T |
C |
3: 87,931,427 (GRCm39) |
|
probably null |
Het |
Incenp |
G |
T |
19: 9,862,851 (GRCm39) |
T401N |
unknown |
Het |
Kalrn |
A |
G |
16: 33,797,894 (GRCm39) |
|
probably null |
Het |
Kcnq3 |
A |
G |
15: 65,900,472 (GRCm39) |
|
probably null |
Het |
Kif21b |
T |
C |
1: 136,098,894 (GRCm39) |
V1394A |
probably damaging |
Het |
Klhl23 |
T |
C |
2: 69,664,030 (GRCm39) |
C460R |
probably damaging |
Het |
L3mbtl1 |
G |
A |
2: 162,801,492 (GRCm39) |
A291T |
probably damaging |
Het |
Lcp1 |
T |
C |
14: 75,437,946 (GRCm39) |
S119P |
probably damaging |
Het |
Ldhc |
A |
G |
7: 46,519,175 (GRCm39) |
I133V |
probably benign |
Het |
Lmntd2 |
G |
A |
7: 140,791,972 (GRCm39) |
|
probably benign |
Het |
Lpl |
A |
T |
8: 69,349,454 (GRCm39) |
K327* |
probably null |
Het |
Lrp1b |
T |
C |
2: 40,765,081 (GRCm39) |
D2801G |
probably damaging |
Het |
Mppe1 |
C |
A |
18: 67,362,843 (GRCm39) |
A131S |
probably benign |
Het |
Msh3 |
T |
A |
13: 92,386,328 (GRCm39) |
|
probably benign |
Het |
Msh5 |
A |
G |
17: 35,252,576 (GRCm39) |
I377T |
probably damaging |
Het |
Myo1e |
T |
C |
9: 70,276,055 (GRCm39) |
F757L |
probably benign |
Het |
Myof |
A |
T |
19: 37,934,082 (GRCm39) |
D955E |
probably damaging |
Het |
Nckap1 |
C |
T |
2: 80,348,286 (GRCm39) |
S889N |
probably benign |
Het |
Ncor2 |
T |
C |
5: 125,115,982 (GRCm39) |
D858G |
probably damaging |
Het |
Neb |
A |
T |
2: 52,153,917 (GRCm39) |
V2398D |
possibly damaging |
Het |
Nefl |
C |
G |
14: 68,324,121 (GRCm39) |
T453R |
probably benign |
Het |
Nf1 |
A |
G |
11: 79,444,787 (GRCm39) |
N371D |
probably benign |
Het |
Nhsl3 |
A |
G |
4: 129,119,810 (GRCm39) |
|
probably benign |
Het |
Nlrp4f |
T |
C |
13: 65,341,905 (GRCm39) |
Y580C |
probably damaging |
Het |
Nme8 |
A |
C |
13: 19,836,492 (GRCm39) |
L228R |
probably damaging |
Het |
Numa1 |
C |
T |
7: 101,658,529 (GRCm39) |
A1605V |
probably damaging |
Het |
Ofd1 |
T |
C |
X: 165,210,210 (GRCm39) |
Y205C |
probably benign |
Het |
Or2ag12 |
T |
A |
7: 106,276,877 (GRCm39) |
N272I |
probably damaging |
Het |
Or2d3b |
G |
A |
7: 106,513,453 (GRCm39) |
G16D |
probably damaging |
Het |
Or4k77 |
C |
T |
2: 111,199,421 (GRCm39) |
S148L |
probably benign |
Het |
Or8g55 |
T |
A |
9: 39,785,234 (GRCm39) |
I221N |
probably damaging |
Het |
Or8k3 |
T |
A |
2: 86,058,596 (GRCm39) |
T240S |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,763,487 (GRCm39) |
T3987A |
unknown |
Het |
Pdgfrb |
G |
A |
18: 61,199,566 (GRCm39) |
|
probably benign |
Het |
Pdxk |
G |
A |
10: 78,276,988 (GRCm39) |
T270I |
probably damaging |
Het |
Pex5 |
T |
C |
6: 124,391,364 (GRCm39) |
E10G |
probably damaging |
Het |
Pik3c2g |
T |
A |
6: 139,846,112 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
T |
A |
1: 20,451,747 (GRCm39) |
I2183F |
probably damaging |
Het |
Plppr2 |
T |
C |
9: 21,852,422 (GRCm39) |
V102A |
probably damaging |
Het |
Plxnd1 |
T |
C |
6: 115,939,478 (GRCm39) |
T1449A |
probably damaging |
Het |
Pnkd |
T |
A |
1: 74,325,069 (GRCm39) |
|
probably null |
Het |
Pom121l2 |
A |
G |
13: 22,167,642 (GRCm39) |
I638V |
probably damaging |
Het |
Prag1 |
A |
G |
8: 36,596,314 (GRCm39) |
|
probably null |
Het |
Ranbp10 |
A |
G |
8: 106,513,340 (GRCm39) |
F191L |
probably damaging |
Het |
Rapgef1 |
T |
C |
2: 29,623,723 (GRCm39) |
L824P |
probably damaging |
Het |
Rec8 |
T |
C |
14: 55,861,599 (GRCm39) |
L418P |
probably damaging |
Het |
Rimbp2 |
T |
A |
5: 128,874,305 (GRCm39) |
N429Y |
probably damaging |
Het |
Rpe65 |
C |
A |
3: 159,321,307 (GRCm39) |
T373K |
probably benign |
Het |
Rpl35rt |
T |
G |
1: 156,194,017 (GRCm39) |
*124G |
probably null |
Het |
Rrn3 |
T |
C |
16: 13,606,938 (GRCm39) |
S151P |
probably damaging |
Het |
Scn7a |
A |
G |
2: 66,514,633 (GRCm39) |
V1047A |
possibly damaging |
Het |
Scn9a |
G |
T |
2: 66,345,724 (GRCm39) |
P1123Q |
probably damaging |
Het |
Secisbp2l |
T |
C |
2: 125,589,430 (GRCm39) |
D706G |
probably damaging |
Het |
Serpina5 |
A |
T |
12: 104,070,116 (GRCm39) |
T338S |
probably benign |
Het |
Sez6 |
G |
A |
11: 77,844,894 (GRCm39) |
|
probably null |
Het |
Shisa4 |
C |
T |
1: 135,300,012 (GRCm39) |
G157D |
probably damaging |
Het |
Slc1a7 |
G |
T |
4: 107,825,782 (GRCm39) |
D14Y |
probably benign |
Het |
Slc25a11 |
A |
C |
11: 70,536,999 (GRCm39) |
L51V |
probably benign |
Het |
Slit3 |
A |
G |
11: 35,521,668 (GRCm39) |
|
probably null |
Het |
Spata13 |
G |
T |
14: 60,928,912 (GRCm39) |
G157W |
probably damaging |
Het |
Spta1 |
T |
C |
1: 174,067,933 (GRCm39) |
V2120A |
possibly damaging |
Het |
Srpra |
T |
C |
9: 35,124,834 (GRCm39) |
|
probably null |
Het |
Syt6 |
A |
G |
3: 103,494,736 (GRCm39) |
I234V |
probably benign |
Het |
Thada |
G |
T |
17: 84,617,470 (GRCm39) |
P1349T |
probably damaging |
Het |
Tmem161a |
C |
T |
8: 70,629,559 (GRCm39) |
R58W |
probably damaging |
Het |
Top3b |
A |
G |
16: 16,701,383 (GRCm39) |
I232V |
probably damaging |
Het |
Tspan1 |
T |
A |
4: 116,020,826 (GRCm39) |
Q197L |
possibly damaging |
Het |
Ttc28 |
A |
C |
5: 111,383,501 (GRCm39) |
Y1334S |
probably benign |
Het |
Ubxn6 |
G |
T |
17: 56,380,077 (GRCm39) |
N28K |
possibly damaging |
Het |
Uggt1 |
T |
C |
1: 36,190,862 (GRCm39) |
D1366G |
probably damaging |
Het |
Ugp2 |
A |
G |
11: 21,278,942 (GRCm39) |
S415P |
probably damaging |
Het |
Vcan |
A |
T |
13: 89,837,157 (GRCm39) |
S2796T |
probably damaging |
Het |
Vipr2 |
T |
C |
12: 116,099,826 (GRCm39) |
V231A |
probably benign |
Het |
Vmn1r176 |
T |
C |
7: 23,534,373 (GRCm39) |
N260S |
probably benign |
Het |
Vmn1r59 |
A |
T |
7: 5,457,038 (GRCm39) |
Y241N |
probably damaging |
Het |
Vmn2r67 |
A |
T |
7: 84,801,013 (GRCm39) |
Y308N |
probably benign |
Het |
Vmn2r75 |
A |
T |
7: 85,797,470 (GRCm39) |
M781K |
probably damaging |
Het |
Vwa3a |
A |
T |
7: 120,379,394 (GRCm39) |
I500F |
probably damaging |
Het |
Zfp609 |
A |
G |
9: 65,702,559 (GRCm39) |
V31A |
probably damaging |
Het |
Zfp689 |
G |
T |
7: 127,043,959 (GRCm39) |
Q224K |
probably damaging |
Het |
Zfp81 |
A |
T |
17: 33,554,475 (GRCm39) |
L113H |
probably benign |
Het |
|
Other mutations in Abca17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Abca17
|
APN |
17 |
24,514,165 (GRCm39) |
missense |
probably benign |
0.14 |
IGL00585:Abca17
|
APN |
17 |
24,519,294 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00941:Abca17
|
APN |
17 |
24,536,104 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01987:Abca17
|
APN |
17 |
24,565,202 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01988:Abca17
|
APN |
17 |
24,553,229 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02223:Abca17
|
APN |
17 |
24,506,909 (GRCm39) |
nonsense |
probably null |
|
IGL02368:Abca17
|
APN |
17 |
24,506,767 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02405:Abca17
|
APN |
17 |
24,498,036 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02431:Abca17
|
APN |
17 |
24,517,958 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02607:Abca17
|
APN |
17 |
24,546,679 (GRCm39) |
nonsense |
probably null |
|
IGL02706:Abca17
|
APN |
17 |
24,517,966 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02729:Abca17
|
APN |
17 |
24,499,455 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02818:Abca17
|
APN |
17 |
24,519,326 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02891:Abca17
|
APN |
17 |
24,500,340 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03236:Abca17
|
APN |
17 |
24,545,450 (GRCm39) |
splice site |
probably benign |
|
IGL03299:Abca17
|
APN |
17 |
24,484,565 (GRCm39) |
missense |
probably damaging |
1.00 |
basin
|
UTSW |
17 |
24,537,159 (GRCm39) |
missense |
probably benign |
0.01 |
Bowl
|
UTSW |
17 |
24,536,212 (GRCm39) |
missense |
probably benign |
0.09 |
R0018:Abca17
|
UTSW |
17 |
24,532,162 (GRCm39) |
splice site |
probably null |
|
R0467:Abca17
|
UTSW |
17 |
24,532,151 (GRCm39) |
splice site |
probably benign |
|
R0671:Abca17
|
UTSW |
17 |
24,500,223 (GRCm39) |
missense |
probably benign |
0.00 |
R1175:Abca17
|
UTSW |
17 |
24,508,325 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1397:Abca17
|
UTSW |
17 |
24,504,733 (GRCm39) |
missense |
probably benign |
0.18 |
R1398:Abca17
|
UTSW |
17 |
24,547,511 (GRCm39) |
missense |
probably damaging |
0.96 |
R1678:Abca17
|
UTSW |
17 |
24,554,594 (GRCm39) |
missense |
probably benign |
0.05 |
R1696:Abca17
|
UTSW |
17 |
24,486,632 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1781:Abca17
|
UTSW |
17 |
24,486,531 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1845:Abca17
|
UTSW |
17 |
24,486,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R1997:Abca17
|
UTSW |
17 |
24,504,700 (GRCm39) |
missense |
probably benign |
0.02 |
R2141:Abca17
|
UTSW |
17 |
24,553,240 (GRCm39) |
missense |
probably benign |
0.00 |
R2199:Abca17
|
UTSW |
17 |
24,554,598 (GRCm39) |
missense |
probably benign |
0.19 |
R2394:Abca17
|
UTSW |
17 |
24,500,190 (GRCm39) |
splice site |
probably null |
|
R2442:Abca17
|
UTSW |
17 |
24,547,606 (GRCm39) |
missense |
probably benign |
0.02 |
R2509:Abca17
|
UTSW |
17 |
24,508,587 (GRCm39) |
splice site |
probably benign |
|
R2848:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
R2849:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
R2859:Abca17
|
UTSW |
17 |
24,500,288 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2879:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
R2935:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
R3153:Abca17
|
UTSW |
17 |
24,547,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R3154:Abca17
|
UTSW |
17 |
24,547,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R3434:Abca17
|
UTSW |
17 |
24,508,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R3695:Abca17
|
UTSW |
17 |
24,508,481 (GRCm39) |
missense |
probably damaging |
0.96 |
R3905:Abca17
|
UTSW |
17 |
24,515,257 (GRCm39) |
missense |
probably benign |
0.13 |
R4282:Abca17
|
UTSW |
17 |
24,518,034 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4334:Abca17
|
UTSW |
17 |
24,537,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R4350:Abca17
|
UTSW |
17 |
24,498,020 (GRCm39) |
critical splice donor site |
probably null |
|
R4548:Abca17
|
UTSW |
17 |
24,553,245 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4626:Abca17
|
UTSW |
17 |
24,540,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R4722:Abca17
|
UTSW |
17 |
24,484,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R4745:Abca17
|
UTSW |
17 |
24,526,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R4818:Abca17
|
UTSW |
17 |
24,536,135 (GRCm39) |
missense |
probably damaging |
0.98 |
R5279:Abca17
|
UTSW |
17 |
24,508,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R5310:Abca17
|
UTSW |
17 |
24,500,204 (GRCm39) |
missense |
probably benign |
0.00 |
R5320:Abca17
|
UTSW |
17 |
24,526,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R5435:Abca17
|
UTSW |
17 |
24,486,588 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5622:Abca17
|
UTSW |
17 |
24,546,642 (GRCm39) |
missense |
probably benign |
0.14 |
R5776:Abca17
|
UTSW |
17 |
24,514,132 (GRCm39) |
missense |
probably benign |
0.09 |
R5928:Abca17
|
UTSW |
17 |
24,537,159 (GRCm39) |
missense |
probably benign |
0.01 |
R6013:Abca17
|
UTSW |
17 |
24,506,820 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6035:Abca17
|
UTSW |
17 |
24,500,219 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6035:Abca17
|
UTSW |
17 |
24,500,219 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6052:Abca17
|
UTSW |
17 |
24,537,165 (GRCm39) |
missense |
probably benign |
0.00 |
R6063:Abca17
|
UTSW |
17 |
24,483,318 (GRCm39) |
missense |
unknown |
|
R6404:Abca17
|
UTSW |
17 |
24,484,892 (GRCm39) |
missense |
probably benign |
0.13 |
R6746:Abca17
|
UTSW |
17 |
24,565,195 (GRCm39) |
nonsense |
probably null |
|
R6819:Abca17
|
UTSW |
17 |
24,506,767 (GRCm39) |
missense |
probably benign |
0.01 |
R6828:Abca17
|
UTSW |
17 |
24,545,389 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7043:Abca17
|
UTSW |
17 |
24,484,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R7065:Abca17
|
UTSW |
17 |
24,546,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R7123:Abca17
|
UTSW |
17 |
24,484,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R7157:Abca17
|
UTSW |
17 |
24,554,564 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7188:Abca17
|
UTSW |
17 |
24,554,600 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7294:Abca17
|
UTSW |
17 |
24,539,983 (GRCm39) |
missense |
not run |
|
R7352:Abca17
|
UTSW |
17 |
24,508,028 (GRCm39) |
nonsense |
probably null |
|
R7355:Abca17
|
UTSW |
17 |
24,486,621 (GRCm39) |
missense |
probably benign |
0.00 |
R7358:Abca17
|
UTSW |
17 |
24,510,529 (GRCm39) |
missense |
probably benign |
0.00 |
R7411:Abca17
|
UTSW |
17 |
24,547,543 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7915:Abca17
|
UTSW |
17 |
24,484,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R8039:Abca17
|
UTSW |
17 |
24,547,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R8095:Abca17
|
UTSW |
17 |
24,536,196 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8308:Abca17
|
UTSW |
17 |
24,486,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R8517:Abca17
|
UTSW |
17 |
24,536,207 (GRCm39) |
missense |
probably benign |
0.00 |
R8811:Abca17
|
UTSW |
17 |
24,536,212 (GRCm39) |
missense |
probably benign |
0.09 |
R8819:Abca17
|
UTSW |
17 |
24,547,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R8820:Abca17
|
UTSW |
17 |
24,547,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R8953:Abca17
|
UTSW |
17 |
24,518,015 (GRCm39) |
missense |
probably benign |
|
R9095:Abca17
|
UTSW |
17 |
24,500,370 (GRCm39) |
missense |
probably damaging |
0.97 |
R9313:Abca17
|
UTSW |
17 |
24,565,207 (GRCm39) |
missense |
probably benign |
0.00 |
R9314:Abca17
|
UTSW |
17 |
24,547,593 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9347:Abca17
|
UTSW |
17 |
24,483,479 (GRCm39) |
missense |
probably benign |
|
R9351:Abca17
|
UTSW |
17 |
24,510,751 (GRCm39) |
missense |
probably benign |
0.00 |
R9387:Abca17
|
UTSW |
17 |
24,553,255 (GRCm39) |
missense |
probably benign |
0.02 |
R9388:Abca17
|
UTSW |
17 |
24,483,273 (GRCm39) |
missense |
unknown |
|
R9440:Abca17
|
UTSW |
17 |
24,499,452 (GRCm39) |
missense |
probably benign |
0.02 |
R9498:Abca17
|
UTSW |
17 |
24,484,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R9654:Abca17
|
UTSW |
17 |
24,536,099 (GRCm39) |
missense |
probably benign |
0.09 |
R9709:Abca17
|
UTSW |
17 |
24,517,934 (GRCm39) |
missense |
probably benign |
|
R9770:Abca17
|
UTSW |
17 |
24,514,121 (GRCm39) |
missense |
probably benign |
0.00 |
R9773:Abca17
|
UTSW |
17 |
24,508,565 (GRCm39) |
missense |
probably damaging |
1.00 |
RF024:Abca17
|
UTSW |
17 |
24,506,706 (GRCm39) |
frame shift |
probably null |
|
RF029:Abca17
|
UTSW |
17 |
24,506,701 (GRCm39) |
critical splice donor site |
probably benign |
|
RF032:Abca17
|
UTSW |
17 |
24,506,701 (GRCm39) |
frame shift |
probably null |
|
RF036:Abca17
|
UTSW |
17 |
24,506,701 (GRCm39) |
critical splice donor site |
probably benign |
|
X0017:Abca17
|
UTSW |
17 |
24,536,137 (GRCm39) |
missense |
probably benign |
0.26 |
X0065:Abca17
|
UTSW |
17 |
24,553,258 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Abca17
|
UTSW |
17 |
24,498,081 (GRCm39) |
missense |
probably benign |
0.03 |
Z1088:Abca17
|
UTSW |
17 |
24,498,053 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1088:Abca17
|
UTSW |
17 |
24,565,193 (GRCm39) |
missense |
probably damaging |
0.98 |
|