Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adprhl1 |
T |
C |
8: 13,274,511 (GRCm39) |
D749G |
probably benign |
Het |
Ank1 |
T |
A |
8: 23,598,241 (GRCm39) |
I782N |
probably damaging |
Het |
Arap2 |
T |
A |
5: 62,888,037 (GRCm39) |
Q436H |
probably damaging |
Het |
Baz2b |
A |
C |
2: 59,755,149 (GRCm39) |
F269L |
probably damaging |
Het |
Bivm |
C |
T |
1: 44,158,439 (GRCm39) |
|
probably benign |
Het |
Brsk1 |
A |
T |
7: 4,711,089 (GRCm39) |
D603V |
probably damaging |
Het |
C2cd3 |
C |
T |
7: 100,104,004 (GRCm39) |
P2006S |
probably benign |
Het |
Cacna1a |
T |
C |
8: 85,313,764 (GRCm39) |
F1513L |
probably benign |
Het |
Cdin1 |
T |
A |
2: 115,505,265 (GRCm39) |
S179T |
probably benign |
Het |
Cep128 |
C |
T |
12: 91,263,006 (GRCm39) |
E298K |
probably damaging |
Het |
Cfap74 |
A |
G |
4: 155,531,152 (GRCm39) |
T802A |
unknown |
Het |
Cnbd2 |
G |
A |
2: 156,154,460 (GRCm39) |
R3Q |
unknown |
Het |
Cul9 |
TTCCTCCTCCTCCTCCTCCTCCTC |
TTCCTCCTCCTCCTCCTCCTC |
17: 46,811,775 (GRCm39) |
|
probably benign |
Het |
Defa28 |
C |
T |
8: 22,073,840 (GRCm39) |
T81I |
|
Het |
Dync1h1 |
A |
G |
12: 110,608,477 (GRCm39) |
D2735G |
probably damaging |
Het |
Eif5b |
A |
T |
1: 38,090,300 (GRCm39) |
I1160F |
possibly damaging |
Het |
Fzd9 |
T |
C |
5: 135,279,178 (GRCm39) |
M236V |
possibly damaging |
Het |
H2ac7 |
A |
G |
13: 23,758,664 (GRCm39) |
Q7R |
unknown |
Het |
Haus6 |
A |
G |
4: 86,501,364 (GRCm39) |
S836P |
possibly damaging |
Het |
Hdac5 |
T |
A |
11: 102,097,512 (GRCm39) |
K167I |
possibly damaging |
Het |
Heatr5b |
C |
G |
17: 79,069,424 (GRCm39) |
|
probably benign |
Het |
Impdh1 |
G |
A |
6: 29,216,248 (GRCm39) |
|
probably benign |
Het |
Iqgap3 |
T |
C |
3: 87,997,193 (GRCm39) |
I192T |
probably damaging |
Het |
Lama1 |
C |
T |
17: 68,112,367 (GRCm39) |
A2269V |
|
Het |
Lamb3 |
A |
G |
1: 193,014,644 (GRCm39) |
N601S |
probably damaging |
Het |
Ltbp2 |
G |
T |
12: 84,875,316 (GRCm39) |
N569K |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,304,323 (GRCm39) |
S60G |
probably benign |
Het |
Marchf6 |
A |
T |
15: 31,498,850 (GRCm39) |
V149E |
probably damaging |
Het |
Mcu |
A |
G |
10: 59,287,078 (GRCm39) |
S160P |
probably benign |
Het |
Miga1 |
A |
G |
3: 151,982,294 (GRCm39) |
L594P |
probably damaging |
Het |
Mindy4 |
T |
C |
6: 55,255,223 (GRCm39) |
L567P |
probably benign |
Het |
Ndst2 |
A |
G |
14: 20,774,830 (GRCm39) |
I791T |
probably benign |
Het |
Nebl |
A |
T |
2: 17,735,671 (GRCm39) |
M1K |
probably null |
Het |
Or2bd2 |
T |
C |
7: 6,443,285 (GRCm39) |
C129R |
probably damaging |
Het |
Or5c1 |
A |
G |
2: 37,222,388 (GRCm39) |
I210V |
probably damaging |
Het |
Ormdl1 |
A |
T |
1: 53,344,708 (GRCm39) |
D90V |
probably damaging |
Het |
Pank1 |
A |
T |
19: 34,804,903 (GRCm39) |
|
probably benign |
Het |
Pcdhac2 |
T |
A |
18: 37,277,071 (GRCm39) |
L17Q |
probably benign |
Het |
Pde3a |
A |
T |
6: 141,405,522 (GRCm39) |
D458V |
probably damaging |
Het |
Pgm1 |
T |
G |
4: 99,824,297 (GRCm39) |
N323K |
probably damaging |
Het |
Pigt |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
CCAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGATCTGTAACCACAGGCCAGTGAGTAGGTTTGTCTCTGTCTAGTGTGGAT |
2: 164,341,589 (GRCm39) |
|
probably null |
Het |
Pigw |
A |
T |
11: 84,767,961 (GRCm39) |
I456K |
possibly damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Plxnc1 |
T |
A |
10: 94,685,709 (GRCm39) |
I761L |
probably benign |
Het |
Pramel22 |
A |
T |
4: 143,382,060 (GRCm39) |
M212K |
probably damaging |
Het |
Prkaca |
A |
G |
8: 84,717,151 (GRCm39) |
N172D |
probably damaging |
Het |
Rab3b |
A |
C |
4: 108,797,925 (GRCm39) |
D192A |
probably benign |
Het |
Rims2 |
T |
C |
15: 39,398,350 (GRCm39) |
L1105P |
probably benign |
Het |
Rinl |
T |
A |
7: 28,491,747 (GRCm39) |
I100N |
probably damaging |
Het |
Rnf13 |
T |
G |
3: 57,714,520 (GRCm39) |
I193S |
probably damaging |
Het |
Sik2 |
A |
T |
9: 50,810,026 (GRCm39) |
S512R |
probably damaging |
Het |
Snx17 |
A |
G |
5: 31,353,887 (GRCm39) |
Y225C |
probably damaging |
Het |
Spata13 |
A |
T |
14: 60,987,524 (GRCm39) |
D894V |
probably damaging |
Het |
Spx |
A |
G |
6: 142,360,543 (GRCm39) |
D65G |
probably damaging |
Het |
Syne1 |
G |
T |
10: 5,299,020 (GRCm39) |
S1022* |
probably null |
Het |
Tchh |
C |
T |
3: 93,354,957 (GRCm39) |
Q1466* |
probably null |
Het |
Tmem120b |
T |
C |
5: 123,254,302 (GRCm39) |
L292P |
probably damaging |
Het |
Vmn2r10 |
T |
C |
5: 109,143,677 (GRCm39) |
T758A |
probably benign |
Het |
Vmn2r45 |
C |
T |
7: 8,488,619 (GRCm39) |
C137Y |
probably damaging |
Het |
Zfp994 |
A |
G |
17: 22,424,306 (GRCm39) |
S4P |
probably damaging |
Het |
|
Other mutations in Rnf213 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Rnf213
|
APN |
11 |
119,340,169 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00961:Rnf213
|
APN |
11 |
119,331,669 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL01324:Rnf213
|
APN |
11 |
119,338,063 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01351:Rnf213
|
APN |
11 |
119,373,944 (GRCm39) |
missense |
probably benign |
0.25 |
IGL01403:Rnf213
|
APN |
11 |
119,334,126 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01704:Rnf213
|
APN |
11 |
119,340,702 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01765:Rnf213
|
APN |
11 |
119,327,178 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01803:Rnf213
|
APN |
11 |
119,332,133 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01804:Rnf213
|
APN |
11 |
119,333,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01900:Rnf213
|
APN |
11 |
119,333,841 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01944:Rnf213
|
APN |
11 |
119,307,283 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01982:Rnf213
|
APN |
11 |
119,334,094 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02008:Rnf213
|
APN |
11 |
119,309,135 (GRCm39) |
splice site |
probably benign |
|
IGL02084:Rnf213
|
APN |
11 |
119,336,499 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02253:Rnf213
|
APN |
11 |
119,331,476 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02254:Rnf213
|
APN |
11 |
119,371,733 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02296:Rnf213
|
APN |
11 |
119,354,162 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02531:Rnf213
|
APN |
11 |
119,327,628 (GRCm39) |
missense |
probably benign |
|
IGL02588:Rnf213
|
APN |
11 |
119,307,362 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02615:Rnf213
|
APN |
11 |
119,331,615 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02805:Rnf213
|
APN |
11 |
119,325,892 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02887:Rnf213
|
APN |
11 |
119,318,336 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03001:Rnf213
|
APN |
11 |
119,370,767 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03035:Rnf213
|
APN |
11 |
119,336,452 (GRCm39) |
splice site |
probably benign |
|
IGL03057:Rnf213
|
APN |
11 |
119,331,913 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03148:Rnf213
|
APN |
11 |
119,355,833 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03308:Rnf213
|
APN |
11 |
119,364,998 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03339:Rnf213
|
APN |
11 |
119,333,830 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03369:Rnf213
|
APN |
11 |
119,312,294 (GRCm39) |
missense |
probably benign |
0.34 |
attrition
|
UTSW |
11 |
119,321,147 (GRCm39) |
missense |
possibly damaging |
0.77 |
defame
|
UTSW |
11 |
119,321,107 (GRCm39) |
nonsense |
probably null |
|
Derogate
|
UTSW |
11 |
119,361,036 (GRCm39) |
missense |
probably damaging |
1.00 |
dinky
|
UTSW |
11 |
119,307,284 (GRCm39) |
missense |
probably damaging |
0.99 |
G1funyon_rnf213_024
|
UTSW |
11 |
119,325,568 (GRCm39) |
missense |
|
|
Impugn
|
UTSW |
11 |
119,327,649 (GRCm39) |
nonsense |
probably null |
|
R4332_Rnf213_642
|
UTSW |
11 |
119,327,502 (GRCm39) |
missense |
probably damaging |
1.00 |
B6584:Rnf213
|
UTSW |
11 |
119,316,895 (GRCm39) |
missense |
probably damaging |
0.97 |
G1Funyon:Rnf213
|
UTSW |
11 |
119,325,568 (GRCm39) |
missense |
|
|
PIT4585001:Rnf213
|
UTSW |
11 |
119,349,218 (GRCm39) |
missense |
|
|
R0008:Rnf213
|
UTSW |
11 |
119,355,878 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0015:Rnf213
|
UTSW |
11 |
119,332,432 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0041:Rnf213
|
UTSW |
11 |
119,293,401 (GRCm39) |
missense |
probably benign |
0.41 |
R0114:Rnf213
|
UTSW |
11 |
119,305,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Rnf213
|
UTSW |
11 |
119,321,187 (GRCm39) |
missense |
probably benign |
0.10 |
R0131:Rnf213
|
UTSW |
11 |
119,321,187 (GRCm39) |
missense |
probably benign |
0.10 |
R0132:Rnf213
|
UTSW |
11 |
119,321,187 (GRCm39) |
missense |
probably benign |
0.10 |
R0138:Rnf213
|
UTSW |
11 |
119,307,322 (GRCm39) |
missense |
probably benign |
0.05 |
R0144:Rnf213
|
UTSW |
11 |
119,370,426 (GRCm39) |
nonsense |
probably null |
|
R0184:Rnf213
|
UTSW |
11 |
119,305,347 (GRCm39) |
missense |
probably damaging |
0.99 |
R0321:Rnf213
|
UTSW |
11 |
119,328,931 (GRCm39) |
nonsense |
probably null |
|
R0365:Rnf213
|
UTSW |
11 |
119,316,937 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0415:Rnf213
|
UTSW |
11 |
119,305,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R0421:Rnf213
|
UTSW |
11 |
119,338,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R0494:Rnf213
|
UTSW |
11 |
119,316,838 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0494:Rnf213
|
UTSW |
11 |
119,333,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R0549:Rnf213
|
UTSW |
11 |
119,355,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R0577:Rnf213
|
UTSW |
11 |
119,334,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R0605:Rnf213
|
UTSW |
11 |
119,322,543 (GRCm39) |
missense |
probably benign |
0.03 |
R0638:Rnf213
|
UTSW |
11 |
119,361,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Rnf213
|
UTSW |
11 |
119,332,660 (GRCm39) |
missense |
probably benign |
0.28 |
R0715:Rnf213
|
UTSW |
11 |
119,331,976 (GRCm39) |
missense |
probably damaging |
0.97 |
R0732:Rnf213
|
UTSW |
11 |
119,331,894 (GRCm39) |
missense |
probably damaging |
0.99 |
R0748:Rnf213
|
UTSW |
11 |
119,364,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R0765:Rnf213
|
UTSW |
11 |
119,313,921 (GRCm39) |
critical splice donor site |
probably null |
|
R0890:Rnf213
|
UTSW |
11 |
119,321,312 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0927:Rnf213
|
UTSW |
11 |
119,305,396 (GRCm39) |
missense |
probably benign |
0.00 |
R0940:Rnf213
|
UTSW |
11 |
119,307,389 (GRCm39) |
missense |
probably benign |
0.10 |
R0959:Rnf213
|
UTSW |
11 |
119,343,407 (GRCm39) |
missense |
probably damaging |
0.99 |
R1077:Rnf213
|
UTSW |
11 |
119,376,824 (GRCm39) |
splice site |
probably benign |
|
R1104:Rnf213
|
UTSW |
11 |
119,368,055 (GRCm39) |
missense |
probably benign |
0.29 |
R1141:Rnf213
|
UTSW |
11 |
119,326,809 (GRCm39) |
missense |
probably benign |
0.02 |
R1219:Rnf213
|
UTSW |
11 |
119,327,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1435:Rnf213
|
UTSW |
11 |
119,326,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R1444:Rnf213
|
UTSW |
11 |
119,333,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R1474:Rnf213
|
UTSW |
11 |
119,328,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R1488:Rnf213
|
UTSW |
11 |
119,371,715 (GRCm39) |
missense |
probably benign |
0.05 |
R1523:Rnf213
|
UTSW |
11 |
119,332,714 (GRCm39) |
missense |
probably damaging |
1.00 |
R1548:Rnf213
|
UTSW |
11 |
119,333,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R1554:Rnf213
|
UTSW |
11 |
119,332,665 (GRCm39) |
missense |
probably benign |
0.06 |
R1563:Rnf213
|
UTSW |
11 |
119,305,352 (GRCm39) |
missense |
probably benign |
0.13 |
R1572:Rnf213
|
UTSW |
11 |
119,327,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R1585:Rnf213
|
UTSW |
11 |
119,354,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R1635:Rnf213
|
UTSW |
11 |
119,333,405 (GRCm39) |
missense |
probably damaging |
0.97 |
R1663:Rnf213
|
UTSW |
11 |
119,328,498 (GRCm39) |
missense |
probably benign |
0.01 |
R1789:Rnf213
|
UTSW |
11 |
119,331,047 (GRCm39) |
missense |
probably damaging |
0.97 |
R1844:Rnf213
|
UTSW |
11 |
119,332,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R1871:Rnf213
|
UTSW |
11 |
119,340,955 (GRCm39) |
missense |
probably benign |
0.08 |
R1893:Rnf213
|
UTSW |
11 |
119,307,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R1937:Rnf213
|
UTSW |
11 |
119,322,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R1967:Rnf213
|
UTSW |
11 |
119,371,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R1987:Rnf213
|
UTSW |
11 |
119,331,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R2000:Rnf213
|
UTSW |
11 |
119,326,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R2020:Rnf213
|
UTSW |
11 |
119,352,744 (GRCm39) |
missense |
probably damaging |
0.99 |
R2100:Rnf213
|
UTSW |
11 |
119,358,128 (GRCm39) |
nonsense |
probably null |
|
R2109:Rnf213
|
UTSW |
11 |
119,333,489 (GRCm39) |
nonsense |
probably null |
|
R2115:Rnf213
|
UTSW |
11 |
119,318,839 (GRCm39) |
missense |
probably benign |
0.00 |
R2126:Rnf213
|
UTSW |
11 |
119,341,027 (GRCm39) |
missense |
probably damaging |
0.99 |
R2144:Rnf213
|
UTSW |
11 |
119,334,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R2145:Rnf213
|
UTSW |
11 |
119,306,019 (GRCm39) |
missense |
probably benign |
0.03 |
R2168:Rnf213
|
UTSW |
11 |
119,305,896 (GRCm39) |
missense |
probably damaging |
0.97 |
R2189:Rnf213
|
UTSW |
11 |
119,321,187 (GRCm39) |
missense |
probably benign |
0.10 |
R2199:Rnf213
|
UTSW |
11 |
119,350,835 (GRCm39) |
missense |
probably benign |
0.01 |
R2220:Rnf213
|
UTSW |
11 |
119,327,254 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2336:Rnf213
|
UTSW |
11 |
119,305,430 (GRCm39) |
missense |
probably benign |
0.02 |
R2400:Rnf213
|
UTSW |
11 |
119,334,021 (GRCm39) |
missense |
probably damaging |
1.00 |
R2679:Rnf213
|
UTSW |
11 |
119,350,764 (GRCm39) |
splice site |
probably null |
|
R2698:Rnf213
|
UTSW |
11 |
119,300,970 (GRCm39) |
missense |
probably benign |
0.26 |
R3151:Rnf213
|
UTSW |
11 |
119,359,718 (GRCm39) |
missense |
probably benign |
0.03 |
R3607:Rnf213
|
UTSW |
11 |
119,332,802 (GRCm39) |
nonsense |
probably null |
|
R3808:Rnf213
|
UTSW |
11 |
119,370,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R3854:Rnf213
|
UTSW |
11 |
119,371,765 (GRCm39) |
splice site |
probably benign |
|
R3856:Rnf213
|
UTSW |
11 |
119,371,765 (GRCm39) |
splice site |
probably benign |
|
R3973:Rnf213
|
UTSW |
11 |
119,359,879 (GRCm39) |
missense |
|
|
R4014:Rnf213
|
UTSW |
11 |
119,336,555 (GRCm39) |
nonsense |
probably null |
|
R4049:Rnf213
|
UTSW |
11 |
119,373,274 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4130:Rnf213
|
UTSW |
11 |
119,373,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R4153:Rnf213
|
UTSW |
11 |
119,300,308 (GRCm39) |
missense |
probably benign |
0.27 |
R4167:Rnf213
|
UTSW |
11 |
119,332,069 (GRCm39) |
missense |
probably damaging |
0.99 |
R4224:Rnf213
|
UTSW |
11 |
119,327,649 (GRCm39) |
nonsense |
probably null |
|
R4332:Rnf213
|
UTSW |
11 |
119,327,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R4415:Rnf213
|
UTSW |
11 |
119,374,790 (GRCm39) |
missense |
probably damaging |
0.99 |
R4547:Rnf213
|
UTSW |
11 |
119,370,496 (GRCm39) |
critical splice donor site |
probably null |
|
R4609:Rnf213
|
UTSW |
11 |
119,328,521 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4684:Rnf213
|
UTSW |
11 |
119,331,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R4704:Rnf213
|
UTSW |
11 |
119,331,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Rnf213
|
UTSW |
11 |
119,310,893 (GRCm39) |
missense |
probably benign |
0.38 |
R4751:Rnf213
|
UTSW |
11 |
119,336,571 (GRCm39) |
missense |
probably benign |
0.12 |
R4828:Rnf213
|
UTSW |
11 |
119,307,455 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4837:Rnf213
|
UTSW |
11 |
119,333,589 (GRCm39) |
missense |
probably benign |
0.00 |
R4894:Rnf213
|
UTSW |
11 |
119,372,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Rnf213
|
UTSW |
11 |
119,318,983 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5026:Rnf213
|
UTSW |
11 |
119,327,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R5034:Rnf213
|
UTSW |
11 |
119,301,633 (GRCm39) |
missense |
probably damaging |
0.99 |
R5284:Rnf213
|
UTSW |
11 |
119,349,692 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5295:Rnf213
|
UTSW |
11 |
119,331,642 (GRCm39) |
missense |
probably benign |
0.00 |
R5406:Rnf213
|
UTSW |
11 |
119,331,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R5441:Rnf213
|
UTSW |
11 |
119,299,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R5449:Rnf213
|
UTSW |
11 |
119,305,902 (GRCm39) |
missense |
probably benign |
0.44 |
R5520:Rnf213
|
UTSW |
11 |
119,324,325 (GRCm39) |
missense |
probably damaging |
1.00 |
R5636:Rnf213
|
UTSW |
11 |
119,327,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R5636:Rnf213
|
UTSW |
11 |
119,327,455 (GRCm39) |
missense |
probably benign |
0.04 |
R5669:Rnf213
|
UTSW |
11 |
119,349,611 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5670:Rnf213
|
UTSW |
11 |
119,325,512 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5697:Rnf213
|
UTSW |
11 |
119,374,720 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5726:Rnf213
|
UTSW |
11 |
119,307,284 (GRCm39) |
missense |
probably damaging |
0.99 |
R5808:Rnf213
|
UTSW |
11 |
119,327,121 (GRCm39) |
missense |
probably benign |
|
R5861:Rnf213
|
UTSW |
11 |
119,364,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R5903:Rnf213
|
UTSW |
11 |
119,312,195 (GRCm39) |
missense |
probably damaging |
0.98 |
R5949:Rnf213
|
UTSW |
11 |
119,333,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R6022:Rnf213
|
UTSW |
11 |
119,376,836 (GRCm39) |
missense |
probably benign |
0.00 |
R6043:Rnf213
|
UTSW |
11 |
119,332,927 (GRCm39) |
missense |
probably damaging |
0.97 |
R6089:Rnf213
|
UTSW |
11 |
119,307,385 (GRCm39) |
missense |
probably benign |
0.14 |
R6123:Rnf213
|
UTSW |
11 |
119,302,339 (GRCm39) |
missense |
probably damaging |
0.96 |
R6134:Rnf213
|
UTSW |
11 |
119,302,296 (GRCm39) |
missense |
probably damaging |
0.99 |
R6135:Rnf213
|
UTSW |
11 |
119,332,854 (GRCm39) |
missense |
probably benign |
0.02 |
R6146:Rnf213
|
UTSW |
11 |
119,326,825 (GRCm39) |
missense |
probably benign |
0.41 |
R6163:Rnf213
|
UTSW |
11 |
119,349,254 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6272:Rnf213
|
UTSW |
11 |
119,305,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R6333:Rnf213
|
UTSW |
11 |
119,354,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R6370:Rnf213
|
UTSW |
11 |
119,367,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R6456:Rnf213
|
UTSW |
11 |
119,350,792 (GRCm39) |
missense |
probably benign |
0.03 |
R6468:Rnf213
|
UTSW |
11 |
119,343,513 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6579:Rnf213
|
UTSW |
11 |
119,327,106 (GRCm39) |
missense |
probably damaging |
0.96 |
R6648:Rnf213
|
UTSW |
11 |
119,370,746 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6727:Rnf213
|
UTSW |
11 |
119,321,147 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6739:Rnf213
|
UTSW |
11 |
119,333,097 (GRCm39) |
missense |
probably damaging |
1.00 |
R6768:Rnf213
|
UTSW |
11 |
119,333,062 (GRCm39) |
missense |
probably damaging |
0.99 |
R6817:Rnf213
|
UTSW |
11 |
119,353,111 (GRCm39) |
critical splice donor site |
probably null |
|
R6820:Rnf213
|
UTSW |
11 |
119,339,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R6841:Rnf213
|
UTSW |
11 |
119,340,692 (GRCm39) |
missense |
probably benign |
0.26 |
R6934:Rnf213
|
UTSW |
11 |
119,310,893 (GRCm39) |
missense |
probably benign |
0.38 |
R7026:Rnf213
|
UTSW |
11 |
119,370,481 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7094:Rnf213
|
UTSW |
11 |
119,328,430 (GRCm39) |
splice site |
probably null |
|
R7170:Rnf213
|
UTSW |
11 |
119,343,401 (GRCm39) |
missense |
|
|
R7185:Rnf213
|
UTSW |
11 |
119,315,024 (GRCm39) |
missense |
|
|
R7239:Rnf213
|
UTSW |
11 |
119,349,614 (GRCm39) |
missense |
|
|
R7258:Rnf213
|
UTSW |
11 |
119,343,401 (GRCm39) |
missense |
|
|
R7259:Rnf213
|
UTSW |
11 |
119,343,401 (GRCm39) |
missense |
|
|
R7260:Rnf213
|
UTSW |
11 |
119,343,401 (GRCm39) |
missense |
|
|
R7273:Rnf213
|
UTSW |
11 |
119,322,582 (GRCm39) |
splice site |
probably null |
|
R7282:Rnf213
|
UTSW |
11 |
119,328,818 (GRCm39) |
missense |
|
|
R7311:Rnf213
|
UTSW |
11 |
119,307,373 (GRCm39) |
missense |
|
|
R7352:Rnf213
|
UTSW |
11 |
119,334,405 (GRCm39) |
missense |
|
|
R7369:Rnf213
|
UTSW |
11 |
119,321,294 (GRCm39) |
missense |
|
|
R7410:Rnf213
|
UTSW |
11 |
119,325,877 (GRCm39) |
missense |
|
|
R7448:Rnf213
|
UTSW |
11 |
119,372,117 (GRCm39) |
missense |
|
|
R7561:Rnf213
|
UTSW |
11 |
119,332,545 (GRCm39) |
missense |
|
|
R7573:Rnf213
|
UTSW |
11 |
119,349,310 (GRCm39) |
missense |
|
|
R7615:Rnf213
|
UTSW |
11 |
119,358,123 (GRCm39) |
missense |
|
|
R7680:Rnf213
|
UTSW |
11 |
119,370,382 (GRCm39) |
missense |
|
|
R7739:Rnf213
|
UTSW |
11 |
119,301,687 (GRCm39) |
missense |
|
|
R7789:Rnf213
|
UTSW |
11 |
119,361,045 (GRCm39) |
splice site |
probably null |
|
R7806:Rnf213
|
UTSW |
11 |
119,302,371 (GRCm39) |
missense |
|
|
R8031:Rnf213
|
UTSW |
11 |
119,321,107 (GRCm39) |
nonsense |
probably null |
|
R8042:Rnf213
|
UTSW |
11 |
119,332,480 (GRCm39) |
missense |
|
|
R8053:Rnf213
|
UTSW |
11 |
119,293,473 (GRCm39) |
missense |
|
|
R8284:Rnf213
|
UTSW |
11 |
119,318,909 (GRCm39) |
missense |
|
|
R8301:Rnf213
|
UTSW |
11 |
119,325,568 (GRCm39) |
missense |
|
|
R8325:Rnf213
|
UTSW |
11 |
119,321,271 (GRCm39) |
missense |
|
|
R8332:Rnf213
|
UTSW |
11 |
119,374,524 (GRCm39) |
missense |
|
|
R8443:Rnf213
|
UTSW |
11 |
119,340,149 (GRCm39) |
missense |
|
|
R8518:Rnf213
|
UTSW |
11 |
119,353,043 (GRCm39) |
missense |
|
|
R8531:Rnf213
|
UTSW |
11 |
119,365,031 (GRCm39) |
missense |
probably benign |
0.02 |
R8670:Rnf213
|
UTSW |
11 |
119,349,563 (GRCm39) |
missense |
|
|
R8675:Rnf213
|
UTSW |
11 |
119,346,984 (GRCm39) |
missense |
|
|
R8690:Rnf213
|
UTSW |
11 |
119,332,038 (GRCm39) |
missense |
|
|
R8690:Rnf213
|
UTSW |
11 |
119,308,955 (GRCm39) |
missense |
|
|
R8714:Rnf213
|
UTSW |
11 |
119,359,720 (GRCm39) |
missense |
|
|
R8802:Rnf213
|
UTSW |
11 |
119,352,928 (GRCm39) |
missense |
|
|
R8861:Rnf213
|
UTSW |
11 |
119,333,062 (GRCm39) |
missense |
|
|
R8886:Rnf213
|
UTSW |
11 |
119,364,264 (GRCm39) |
missense |
|
|
R8937:Rnf213
|
UTSW |
11 |
119,321,100 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8941:Rnf213
|
UTSW |
11 |
119,305,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R8973:Rnf213
|
UTSW |
11 |
119,352,756 (GRCm39) |
missense |
|
|
R8983:Rnf213
|
UTSW |
11 |
119,321,175 (GRCm39) |
missense |
|
|
R9043:Rnf213
|
UTSW |
11 |
119,349,739 (GRCm39) |
missense |
|
|
R9081:Rnf213
|
UTSW |
11 |
119,357,062 (GRCm39) |
missense |
|
|
R9132:Rnf213
|
UTSW |
11 |
119,374,742 (GRCm39) |
missense |
|
|
R9135:Rnf213
|
UTSW |
11 |
119,299,573 (GRCm39) |
missense |
|
|
R9146:Rnf213
|
UTSW |
11 |
119,334,499 (GRCm39) |
missense |
|
|
R9156:Rnf213
|
UTSW |
11 |
119,331,574 (GRCm39) |
missense |
|
|
R9183:Rnf213
|
UTSW |
11 |
119,318,448 (GRCm39) |
missense |
|
|
R9234:Rnf213
|
UTSW |
11 |
119,340,943 (GRCm39) |
missense |
|
|
R9275:Rnf213
|
UTSW |
11 |
119,326,768 (GRCm39) |
missense |
|
|
R9278:Rnf213
|
UTSW |
11 |
119,326,768 (GRCm39) |
missense |
|
|
R9296:Rnf213
|
UTSW |
11 |
119,334,621 (GRCm39) |
splice site |
probably benign |
|
R9350:Rnf213
|
UTSW |
11 |
119,332,975 (GRCm39) |
missense |
|
|
R9366:Rnf213
|
UTSW |
11 |
119,327,057 (GRCm39) |
missense |
|
|
R9413:Rnf213
|
UTSW |
11 |
119,357,059 (GRCm39) |
missense |
|
|
R9444:Rnf213
|
UTSW |
11 |
119,325,623 (GRCm39) |
missense |
|
|
R9464:Rnf213
|
UTSW |
11 |
119,354,406 (GRCm39) |
missense |
|
|
R9605:Rnf213
|
UTSW |
11 |
119,359,879 (GRCm39) |
missense |
|
|
R9649:Rnf213
|
UTSW |
11 |
119,370,457 (GRCm39) |
missense |
|
|
R9651:Rnf213
|
UTSW |
11 |
119,331,238 (GRCm39) |
missense |
|
|
R9664:Rnf213
|
UTSW |
11 |
119,332,794 (GRCm39) |
missense |
|
|
R9696:Rnf213
|
UTSW |
11 |
119,359,806 (GRCm39) |
missense |
|
|
R9710:Rnf213
|
UTSW |
11 |
119,331,831 (GRCm39) |
missense |
|
|
R9797:Rnf213
|
UTSW |
11 |
119,333,365 (GRCm39) |
missense |
|
|
S24628:Rnf213
|
UTSW |
11 |
119,305,295 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Rnf213
|
UTSW |
11 |
119,332,650 (GRCm39) |
missense |
probably benign |
0.14 |
X0062:Rnf213
|
UTSW |
11 |
119,364,339 (GRCm39) |
missense |
probably benign |
0.05 |
X0064:Rnf213
|
UTSW |
11 |
119,331,289 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Rnf213
|
UTSW |
11 |
119,368,080 (GRCm39) |
missense |
possibly damaging |
0.69 |
Z1176:Rnf213
|
UTSW |
11 |
119,373,824 (GRCm39) |
missense |
|
|
Z1176:Rnf213
|
UTSW |
11 |
119,332,236 (GRCm39) |
missense |
|
|
|