Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr1b |
T |
C |
15: 101,092,722 (GRCm39) |
W122R |
possibly damaging |
Het |
Adgrv1 |
C |
T |
13: 81,592,657 (GRCm39) |
R4294H |
probably benign |
Het |
Afdn |
A |
G |
17: 14,024,315 (GRCm39) |
T74A |
probably damaging |
Het |
Aff3 |
T |
A |
1: 38,247,098 (GRCm39) |
D829V |
probably benign |
Het |
Akr1c12 |
T |
C |
13: 4,325,772 (GRCm39) |
Q107R |
probably benign |
Het |
Apc |
T |
A |
18: 34,402,252 (GRCm39) |
F131I |
probably benign |
Het |
Atosb |
A |
T |
4: 43,033,687 (GRCm39) |
F489I |
probably damaging |
Het |
Atp13a1 |
T |
A |
8: 70,259,424 (GRCm39) |
L1036H |
probably damaging |
Het |
BC035044 |
A |
C |
6: 128,867,855 (GRCm39) |
|
probably benign |
Het |
C1rl |
A |
G |
6: 124,485,535 (GRCm39) |
D302G |
probably benign |
Het |
C2cd6 |
A |
C |
1: 59,117,093 (GRCm39) |
D133E |
probably benign |
Het |
Cacna1c |
T |
A |
6: 118,629,671 (GRCm39) |
Y1061F |
probably damaging |
Het |
Cav1 |
A |
G |
6: 17,308,034 (GRCm39) |
D62G |
probably damaging |
Het |
Ccdc77 |
T |
C |
6: 120,327,242 (GRCm39) |
M68V |
probably damaging |
Het |
Cd55 |
A |
T |
1: 130,375,348 (GRCm39) |
|
probably benign |
Het |
Cdc27 |
C |
A |
11: 104,413,602 (GRCm39) |
A380S |
probably damaging |
Het |
Cenpb |
A |
T |
2: 131,021,477 (GRCm39) |
I107K |
probably damaging |
Het |
Cep135 |
T |
G |
5: 76,769,187 (GRCm39) |
H612Q |
possibly damaging |
Het |
Chd1l |
A |
T |
3: 97,470,849 (GRCm39) |
N815K |
probably damaging |
Het |
Cldn20 |
C |
T |
17: 3,582,992 (GRCm39) |
T55M |
possibly damaging |
Het |
Depdc1a |
A |
T |
3: 159,221,679 (GRCm39) |
I208L |
probably benign |
Het |
Dgkb |
C |
T |
12: 38,134,223 (GRCm39) |
A43V |
possibly damaging |
Het |
Dgkb |
C |
T |
12: 38,654,104 (GRCm39) |
T741I |
probably damaging |
Het |
Dhx16 |
A |
G |
17: 36,197,076 (GRCm39) |
N653S |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,438,329 (GRCm39) |
S3987T |
probably benign |
Het |
Dnai4 |
T |
C |
4: 102,906,758 (GRCm39) |
D685G |
probably damaging |
Het |
Dst |
T |
A |
1: 34,334,277 (GRCm39) |
I4835N |
probably damaging |
Het |
Esrrb |
A |
G |
12: 86,561,114 (GRCm39) |
I288V |
probably damaging |
Het |
Fnta |
C |
T |
8: 26,497,341 (GRCm39) |
W169* |
probably null |
Het |
Golga4 |
T |
C |
9: 118,365,860 (GRCm39) |
L304P |
probably damaging |
Het |
Hace1 |
A |
G |
10: 45,466,362 (GRCm39) |
|
probably null |
Het |
Ino80b |
G |
T |
6: 83,101,112 (GRCm39) |
|
probably null |
Het |
Kcmf1 |
G |
A |
6: 72,820,082 (GRCm39) |
R306C |
probably damaging |
Het |
Lrrc46 |
G |
A |
11: 96,927,305 (GRCm39) |
T92I |
possibly damaging |
Het |
Man2b1 |
T |
C |
8: 85,824,076 (GRCm39) |
V991A |
possibly damaging |
Het |
Mga |
A |
G |
2: 119,776,776 (GRCm39) |
N1770S |
probably damaging |
Het |
Mgat4e |
T |
C |
1: 134,468,944 (GRCm39) |
T367A |
probably benign |
Het |
Mtr |
A |
G |
13: 12,202,992 (GRCm39) |
S1204P |
probably damaging |
Het |
Myo15a |
G |
A |
11: 60,417,487 (GRCm39) |
|
probably null |
Het |
Nktr |
T |
C |
9: 121,560,585 (GRCm39) |
S74P |
probably damaging |
Het |
Noct |
T |
C |
3: 51,157,508 (GRCm39) |
V282A |
possibly damaging |
Het |
Nol11 |
A |
T |
11: 107,071,912 (GRCm39) |
I227K |
possibly damaging |
Het |
Nsd3 |
T |
A |
8: 26,130,646 (GRCm39) |
S4T |
probably damaging |
Het |
Or5m10b |
T |
A |
2: 85,699,714 (GRCm39) |
Y259* |
probably null |
Het |
Or5p64 |
A |
G |
7: 107,855,109 (GRCm39) |
S79P |
probably damaging |
Het |
Pds5a |
T |
A |
5: 65,809,782 (GRCm39) |
L393F |
probably damaging |
Het |
Rc3h2 |
T |
C |
2: 37,272,028 (GRCm39) |
T768A |
probably damaging |
Het |
Rin3 |
A |
T |
12: 102,335,584 (GRCm39) |
E418D |
probably benign |
Het |
Rnf214 |
G |
T |
9: 45,778,886 (GRCm39) |
T586N |
probably damaging |
Het |
Samd4b |
A |
G |
7: 28,101,285 (GRCm39) |
S667P |
probably damaging |
Het |
Sec14l2 |
T |
C |
11: 4,061,161 (GRCm39) |
Y100C |
probably damaging |
Het |
Slc46a2 |
T |
C |
4: 59,914,077 (GRCm39) |
E282G |
probably benign |
Het |
Themis |
A |
C |
10: 28,657,762 (GRCm39) |
N110T |
possibly damaging |
Het |
Tln1 |
C |
A |
4: 43,543,165 (GRCm39) |
S1333I |
probably benign |
Het |
Tmem53 |
T |
C |
4: 117,125,625 (GRCm39) |
V224A |
possibly damaging |
Het |
Tmtc4 |
T |
A |
14: 123,163,391 (GRCm39) |
K664N |
possibly damaging |
Het |
Tnni3k |
T |
C |
3: 154,674,922 (GRCm39) |
D201G |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,912,898 (GRCm39) |
E1681G |
probably damaging |
Het |
Trhde |
A |
T |
10: 114,340,103 (GRCm39) |
D567E |
probably damaging |
Het |
Tsc2 |
T |
C |
17: 24,828,101 (GRCm39) |
M788V |
probably benign |
Het |
Ube3a |
A |
G |
7: 58,926,650 (GRCm39) |
Y476C |
probably damaging |
Het |
Ubiad1 |
T |
C |
4: 148,520,682 (GRCm39) |
N314S |
possibly damaging |
Het |
Unc79 |
T |
A |
12: 103,139,771 (GRCm39) |
N2375K |
probably damaging |
Het |
Vmn2r107 |
A |
T |
17: 20,595,939 (GRCm39) |
I831F |
probably damaging |
Het |
Vwa3b |
T |
A |
1: 37,124,367 (GRCm39) |
C322S |
probably benign |
Het |
Wnk1 |
A |
T |
6: 119,939,916 (GRCm39) |
H238Q |
probably benign |
Het |
Wnk2 |
A |
G |
13: 49,300,081 (GRCm39) |
Y210H |
probably damaging |
Het |
Wwc2 |
T |
C |
8: 48,304,943 (GRCm39) |
D894G |
unknown |
Het |
Yes1 |
T |
A |
5: 32,810,381 (GRCm39) |
F180Y |
probably damaging |
Het |
Yju2b |
T |
C |
8: 84,985,318 (GRCm39) |
E317G |
probably benign |
Het |
Zbtb46 |
T |
C |
2: 181,033,062 (GRCm39) |
Y533C |
probably damaging |
Het |
Zfp57 |
T |
C |
17: 37,316,942 (GRCm39) |
S7P |
possibly damaging |
Het |
Zzef1 |
T |
C |
11: 72,802,090 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Prex2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00497:Prex2
|
APN |
1 |
11,256,876 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL00948:Prex2
|
APN |
1 |
11,240,838 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01087:Prex2
|
APN |
1 |
11,138,328 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01490:Prex2
|
APN |
1 |
11,254,769 (GRCm39) |
splice site |
probably null |
|
IGL01533:Prex2
|
APN |
1 |
11,256,965 (GRCm39) |
nonsense |
probably null |
|
IGL01661:Prex2
|
APN |
1 |
11,278,838 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01668:Prex2
|
APN |
1 |
11,223,869 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01674:Prex2
|
APN |
1 |
11,240,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01716:Prex2
|
APN |
1 |
11,336,278 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01867:Prex2
|
APN |
1 |
11,168,727 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01954:Prex2
|
APN |
1 |
11,210,235 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL01990:Prex2
|
APN |
1 |
11,193,457 (GRCm39) |
splice site |
probably benign |
|
IGL02022:Prex2
|
APN |
1 |
11,367,963 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02130:Prex2
|
APN |
1 |
11,230,386 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02130:Prex2
|
APN |
1 |
11,183,023 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02221:Prex2
|
APN |
1 |
11,131,569 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02369:Prex2
|
APN |
1 |
11,171,393 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02440:Prex2
|
APN |
1 |
11,223,881 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02477:Prex2
|
APN |
1 |
11,274,378 (GRCm39) |
missense |
probably benign |
|
IGL02492:Prex2
|
APN |
1 |
11,194,069 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03051:Prex2
|
APN |
1 |
11,212,889 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03154:Prex2
|
APN |
1 |
11,223,857 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL03158:Prex2
|
APN |
1 |
11,336,291 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03308:Prex2
|
APN |
1 |
11,255,399 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03338:Prex2
|
APN |
1 |
11,210,489 (GRCm39) |
missense |
probably benign |
0.01 |
R0042:Prex2
|
UTSW |
1 |
11,150,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Prex2
|
UTSW |
1 |
11,230,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R0052:Prex2
|
UTSW |
1 |
11,230,380 (GRCm39) |
missense |
probably damaging |
1.00 |
R0138:Prex2
|
UTSW |
1 |
11,355,267 (GRCm39) |
splice site |
probably benign |
|
R0206:Prex2
|
UTSW |
1 |
11,355,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0206:Prex2
|
UTSW |
1 |
11,355,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0208:Prex2
|
UTSW |
1 |
11,355,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0325:Prex2
|
UTSW |
1 |
11,270,281 (GRCm39) |
splice site |
probably null |
|
R0326:Prex2
|
UTSW |
1 |
11,355,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R0390:Prex2
|
UTSW |
1 |
11,159,930 (GRCm39) |
splice site |
probably null |
|
R0492:Prex2
|
UTSW |
1 |
11,256,857 (GRCm39) |
splice site |
probably benign |
|
R0512:Prex2
|
UTSW |
1 |
11,270,157 (GRCm39) |
missense |
probably benign |
|
R0515:Prex2
|
UTSW |
1 |
11,270,098 (GRCm39) |
missense |
probably damaging |
0.99 |
R0894:Prex2
|
UTSW |
1 |
11,252,122 (GRCm39) |
missense |
probably benign |
|
R1259:Prex2
|
UTSW |
1 |
11,359,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R1332:Prex2
|
UTSW |
1 |
11,274,315 (GRCm39) |
missense |
probably damaging |
1.00 |
R1356:Prex2
|
UTSW |
1 |
11,150,316 (GRCm39) |
nonsense |
probably null |
|
R1451:Prex2
|
UTSW |
1 |
11,226,483 (GRCm39) |
missense |
probably benign |
0.01 |
R1488:Prex2
|
UTSW |
1 |
11,263,752 (GRCm39) |
missense |
probably benign |
0.05 |
R1512:Prex2
|
UTSW |
1 |
11,131,554 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1641:Prex2
|
UTSW |
1 |
11,301,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R1667:Prex2
|
UTSW |
1 |
11,256,981 (GRCm39) |
missense |
probably benign |
|
R1678:Prex2
|
UTSW |
1 |
11,355,313 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1736:Prex2
|
UTSW |
1 |
11,160,108 (GRCm39) |
splice site |
probably benign |
|
R1781:Prex2
|
UTSW |
1 |
11,270,179 (GRCm39) |
missense |
probably benign |
0.17 |
R1804:Prex2
|
UTSW |
1 |
11,202,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R1836:Prex2
|
UTSW |
1 |
11,207,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Prex2
|
UTSW |
1 |
11,232,590 (GRCm39) |
nonsense |
probably null |
|
R1900:Prex2
|
UTSW |
1 |
11,232,590 (GRCm39) |
nonsense |
probably null |
|
R2020:Prex2
|
UTSW |
1 |
11,232,536 (GRCm39) |
missense |
probably damaging |
0.98 |
R2114:Prex2
|
UTSW |
1 |
11,256,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Prex2
|
UTSW |
1 |
11,256,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R2436:Prex2
|
UTSW |
1 |
11,336,376 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2902:Prex2
|
UTSW |
1 |
11,278,838 (GRCm39) |
missense |
possibly damaging |
0.77 |
R2915:Prex2
|
UTSW |
1 |
11,240,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R2924:Prex2
|
UTSW |
1 |
11,168,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R2981:Prex2
|
UTSW |
1 |
11,252,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Prex2
|
UTSW |
1 |
11,220,078 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3832:Prex2
|
UTSW |
1 |
11,226,588 (GRCm39) |
splice site |
probably benign |
|
R3870:Prex2
|
UTSW |
1 |
11,230,416 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3963:Prex2
|
UTSW |
1 |
11,180,581 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4012:Prex2
|
UTSW |
1 |
11,254,740 (GRCm39) |
missense |
probably benign |
|
R4030:Prex2
|
UTSW |
1 |
11,278,792 (GRCm39) |
missense |
probably benign |
0.06 |
R4214:Prex2
|
UTSW |
1 |
11,171,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R4214:Prex2
|
UTSW |
1 |
11,355,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R4242:Prex2
|
UTSW |
1 |
11,226,528 (GRCm39) |
missense |
probably benign |
0.06 |
R4490:Prex2
|
UTSW |
1 |
11,232,487 (GRCm39) |
missense |
probably benign |
0.05 |
R4491:Prex2
|
UTSW |
1 |
11,232,487 (GRCm39) |
missense |
probably benign |
0.05 |
R4492:Prex2
|
UTSW |
1 |
11,232,487 (GRCm39) |
missense |
probably benign |
0.05 |
R4561:Prex2
|
UTSW |
1 |
11,254,769 (GRCm39) |
splice site |
probably null |
|
R4624:Prex2
|
UTSW |
1 |
11,359,489 (GRCm39) |
nonsense |
probably null |
|
R4647:Prex2
|
UTSW |
1 |
11,232,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R4657:Prex2
|
UTSW |
1 |
11,136,049 (GRCm39) |
missense |
probably benign |
0.00 |
R4706:Prex2
|
UTSW |
1 |
11,270,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:Prex2
|
UTSW |
1 |
11,138,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R4900:Prex2
|
UTSW |
1 |
11,220,129 (GRCm39) |
splice site |
probably benign |
|
R4922:Prex2
|
UTSW |
1 |
11,240,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R4961:Prex2
|
UTSW |
1 |
11,168,705 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5284:Prex2
|
UTSW |
1 |
11,336,314 (GRCm39) |
nonsense |
probably null |
|
R5305:Prex2
|
UTSW |
1 |
11,177,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R5307:Prex2
|
UTSW |
1 |
11,270,256 (GRCm39) |
missense |
probably damaging |
0.99 |
R5331:Prex2
|
UTSW |
1 |
11,210,235 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5385:Prex2
|
UTSW |
1 |
11,210,204 (GRCm39) |
missense |
probably damaging |
0.99 |
R5574:Prex2
|
UTSW |
1 |
11,210,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R5979:Prex2
|
UTSW |
1 |
11,202,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R6076:Prex2
|
UTSW |
1 |
11,256,174 (GRCm39) |
missense |
probably benign |
0.09 |
R6160:Prex2
|
UTSW |
1 |
11,064,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R6177:Prex2
|
UTSW |
1 |
11,207,001 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6221:Prex2
|
UTSW |
1 |
11,336,236 (GRCm39) |
missense |
probably benign |
0.01 |
R6293:Prex2
|
UTSW |
1 |
11,232,522 (GRCm39) |
missense |
probably benign |
|
R6335:Prex2
|
UTSW |
1 |
11,180,544 (GRCm39) |
missense |
probably benign |
0.13 |
R6401:Prex2
|
UTSW |
1 |
11,256,951 (GRCm39) |
missense |
probably benign |
0.00 |
R6427:Prex2
|
UTSW |
1 |
11,252,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R6564:Prex2
|
UTSW |
1 |
11,171,285 (GRCm39) |
splice site |
probably null |
|
R6734:Prex2
|
UTSW |
1 |
11,150,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R6753:Prex2
|
UTSW |
1 |
11,254,680 (GRCm39) |
missense |
probably damaging |
0.98 |
R6880:Prex2
|
UTSW |
1 |
11,202,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R6973:Prex2
|
UTSW |
1 |
11,182,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R6980:Prex2
|
UTSW |
1 |
11,232,487 (GRCm39) |
missense |
probably benign |
0.05 |
R6987:Prex2
|
UTSW |
1 |
11,240,976 (GRCm39) |
missense |
probably damaging |
0.99 |
R7085:Prex2
|
UTSW |
1 |
11,168,812 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7101:Prex2
|
UTSW |
1 |
11,223,833 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7106:Prex2
|
UTSW |
1 |
11,207,017 (GRCm39) |
missense |
probably benign |
0.33 |
R7319:Prex2
|
UTSW |
1 |
11,232,532 (GRCm39) |
missense |
probably benign |
0.10 |
R7342:Prex2
|
UTSW |
1 |
11,232,549 (GRCm39) |
missense |
probably benign |
0.00 |
R7469:Prex2
|
UTSW |
1 |
11,355,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R7528:Prex2
|
UTSW |
1 |
11,274,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R7592:Prex2
|
UTSW |
1 |
11,193,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R7650:Prex2
|
UTSW |
1 |
11,220,078 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7695:Prex2
|
UTSW |
1 |
11,232,497 (GRCm39) |
missense |
probably benign |
0.00 |
R7720:Prex2
|
UTSW |
1 |
11,252,161 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7733:Prex2
|
UTSW |
1 |
11,252,183 (GRCm39) |
missense |
probably benign |
0.31 |
R7859:Prex2
|
UTSW |
1 |
11,150,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R8247:Prex2
|
UTSW |
1 |
11,270,194 (GRCm39) |
missense |
probably benign |
|
R8300:Prex2
|
UTSW |
1 |
11,301,942 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8345:Prex2
|
UTSW |
1 |
11,270,118 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8352:Prex2
|
UTSW |
1 |
11,355,364 (GRCm39) |
missense |
probably benign |
|
R8352:Prex2
|
UTSW |
1 |
11,355,363 (GRCm39) |
missense |
probably benign |
|
R8410:Prex2
|
UTSW |
1 |
11,223,881 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8452:Prex2
|
UTSW |
1 |
11,355,364 (GRCm39) |
missense |
probably benign |
|
R8452:Prex2
|
UTSW |
1 |
11,355,363 (GRCm39) |
missense |
probably benign |
|
R8885:Prex2
|
UTSW |
1 |
11,240,799 (GRCm39) |
splice site |
probably benign |
|
R8926:Prex2
|
UTSW |
1 |
11,159,930 (GRCm39) |
splice site |
probably null |
|
R8968:Prex2
|
UTSW |
1 |
11,180,562 (GRCm39) |
nonsense |
probably null |
|
R9049:Prex2
|
UTSW |
1 |
11,256,130 (GRCm39) |
missense |
probably damaging |
0.98 |
R9398:Prex2
|
UTSW |
1 |
11,207,028 (GRCm39) |
missense |
probably benign |
0.00 |
R9452:Prex2
|
UTSW |
1 |
11,256,151 (GRCm39) |
missense |
probably benign |
0.01 |
R9549:Prex2
|
UTSW |
1 |
11,256,915 (GRCm39) |
missense |
probably damaging |
1.00 |
RF005:Prex2
|
UTSW |
1 |
11,255,390 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1177:Prex2
|
UTSW |
1 |
11,359,476 (GRCm39) |
critical splice acceptor site |
probably null |
|
|