Other mutations in this stock |
Total: 107 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatf |
T |
C |
11: 84,402,339 (GRCm39) |
I116V |
probably benign |
Het |
Abhd18 |
T |
C |
3: 40,871,123 (GRCm39) |
F94S |
probably damaging |
Het |
Adam28 |
T |
A |
14: 68,868,241 (GRCm39) |
|
probably benign |
Het |
Afg2a |
G |
C |
3: 37,486,312 (GRCm39) |
D345H |
possibly damaging |
Het |
Amn1 |
A |
T |
6: 149,086,634 (GRCm39) |
|
probably benign |
Het |
Arhgap32 |
T |
C |
9: 32,170,199 (GRCm39) |
V993A |
probably damaging |
Het |
Arhgap33 |
A |
T |
7: 30,223,921 (GRCm39) |
S703T |
probably damaging |
Het |
Arhgef1 |
T |
C |
7: 24,618,785 (GRCm39) |
|
probably benign |
Het |
Atg2a |
A |
G |
19: 6,303,407 (GRCm39) |
Y1083C |
probably damaging |
Het |
Atp2a3 |
T |
C |
11: 72,872,731 (GRCm39) |
F760L |
probably damaging |
Het |
B9d1 |
A |
G |
11: 61,403,271 (GRCm39) |
|
probably benign |
Het |
Batf |
C |
T |
12: 85,733,636 (GRCm39) |
|
probably benign |
Het |
BC051019 |
T |
A |
7: 109,317,182 (GRCm39) |
Y170F |
probably benign |
Het |
Bphl |
T |
C |
13: 34,221,754 (GRCm39) |
*37Q |
probably null |
Het |
Cab39l |
T |
C |
14: 59,737,008 (GRCm39) |
S43P |
probably damaging |
Het |
Cad |
A |
G |
5: 31,234,856 (GRCm39) |
|
probably benign |
Het |
Cct4 |
T |
G |
11: 22,946,014 (GRCm39) |
S119A |
probably benign |
Het |
Cd163 |
G |
A |
6: 124,288,408 (GRCm39) |
V280M |
probably damaging |
Het |
Cd86 |
A |
G |
16: 36,438,999 (GRCm39) |
|
probably benign |
Het |
Cdh23 |
G |
A |
10: 60,152,375 (GRCm39) |
|
probably benign |
Het |
Cdhr5 |
A |
G |
7: 140,852,431 (GRCm39) |
F145S |
probably damaging |
Het |
Cdt1 |
T |
C |
8: 123,298,799 (GRCm39) |
S479P |
possibly damaging |
Het |
Ces2g |
T |
C |
8: 105,693,199 (GRCm39) |
V372A |
probably benign |
Het |
Chrna3 |
T |
C |
9: 54,929,562 (GRCm39) |
D92G |
probably damaging |
Het |
Cndp1 |
A |
G |
18: 84,637,658 (GRCm39) |
S359P |
probably benign |
Het |
Cops4 |
A |
G |
5: 100,676,528 (GRCm39) |
Q93R |
probably damaging |
Het |
Dgka |
G |
C |
10: 128,556,952 (GRCm39) |
|
probably benign |
Het |
Dmp1 |
A |
T |
5: 104,360,074 (GRCm39) |
D250V |
probably damaging |
Het |
Dnajb2 |
C |
T |
1: 75,216,278 (GRCm39) |
|
probably benign |
Het |
Dock9 |
T |
C |
14: 121,899,996 (GRCm39) |
T113A |
possibly damaging |
Het |
Egln3 |
T |
A |
12: 54,250,107 (GRCm39) |
I81F |
probably benign |
Het |
Elapor2 |
G |
A |
5: 9,470,723 (GRCm39) |
|
probably null |
Het |
Elovl5 |
T |
C |
9: 77,868,199 (GRCm39) |
V37A |
probably benign |
Het |
Esco1 |
A |
T |
18: 10,594,940 (GRCm39) |
N115K |
probably benign |
Het |
Fat1 |
A |
T |
8: 45,403,579 (GRCm39) |
N110I |
probably damaging |
Het |
Fezf1 |
T |
A |
6: 23,246,054 (GRCm39) |
K370N |
probably damaging |
Het |
Galnt18 |
T |
A |
7: 111,153,771 (GRCm39) |
K284N |
probably damaging |
Het |
Glt8d1 |
C |
A |
14: 30,733,580 (GRCm39) |
T355K |
possibly damaging |
Het |
Gm17455 |
G |
A |
10: 60,239,014 (GRCm39) |
R93H |
possibly damaging |
Het |
Gng8 |
T |
A |
7: 16,629,213 (GRCm39) |
D46E |
probably benign |
Het |
Gpx4 |
T |
C |
10: 79,892,011 (GRCm39) |
|
probably benign |
Het |
Grk2 |
A |
T |
19: 4,341,347 (GRCm39) |
N189K |
probably damaging |
Het |
Grm5 |
T |
C |
7: 87,779,989 (GRCm39) |
V1143A |
probably benign |
Het |
Hibch |
A |
G |
1: 52,942,055 (GRCm39) |
E237G |
possibly damaging |
Het |
Hipk2 |
C |
T |
6: 38,706,924 (GRCm39) |
A682T |
probably benign |
Het |
Hmcn1 |
G |
T |
1: 150,608,543 (GRCm39) |
|
probably benign |
Het |
Htt |
A |
G |
5: 34,979,188 (GRCm39) |
D857G |
possibly damaging |
Het |
Idh2 |
C |
T |
7: 79,748,005 (GRCm39) |
A232T |
probably damaging |
Het |
Igsf8 |
A |
G |
1: 172,146,265 (GRCm39) |
E421G |
probably benign |
Het |
Kif26a |
T |
A |
12: 112,145,905 (GRCm39) |
|
probably null |
Het |
Klhl26 |
T |
C |
8: 70,904,251 (GRCm39) |
Y519C |
probably damaging |
Het |
Lamc1 |
A |
C |
1: 153,122,682 (GRCm39) |
|
probably null |
Het |
Mical3 |
A |
T |
6: 120,936,162 (GRCm39) |
S1455T |
possibly damaging |
Het |
Mitf |
G |
A |
6: 97,971,390 (GRCm39) |
G186S |
probably benign |
Het |
Ms4a15 |
G |
A |
19: 10,958,722 (GRCm39) |
|
probably benign |
Het |
Myo5b |
A |
G |
18: 74,787,038 (GRCm39) |
E481G |
probably damaging |
Het |
Nanos3 |
C |
T |
8: 84,902,763 (GRCm39) |
R133Q |
probably damaging |
Het |
Nbeal2 |
C |
A |
9: 110,456,255 (GRCm39) |
V1686L |
probably damaging |
Het |
Nedd4l |
T |
G |
18: 65,306,092 (GRCm39) |
S335A |
possibly damaging |
Het |
Nos1 |
A |
T |
5: 118,043,539 (GRCm39) |
N605Y |
probably damaging |
Het |
Nyx |
C |
A |
X: 13,353,508 (GRCm39) |
T454K |
probably benign |
Het |
Or52n2 |
A |
G |
7: 104,542,478 (GRCm39) |
L119P |
probably damaging |
Het |
Or8g55 |
T |
A |
9: 39,784,698 (GRCm39) |
N42K |
probably damaging |
Het |
Pcdhb12 |
T |
A |
18: 37,571,148 (GRCm39) |
F765I |
probably benign |
Het |
Pex3 |
C |
T |
10: 13,403,532 (GRCm39) |
G330R |
probably damaging |
Het |
Pfkfb1 |
T |
C |
X: 149,417,609 (GRCm39) |
Y339H |
probably damaging |
Het |
Pias1 |
G |
A |
9: 62,794,593 (GRCm39) |
Q26* |
probably null |
Het |
Pik3cg |
C |
A |
12: 32,254,545 (GRCm39) |
V481L |
possibly damaging |
Het |
Plcg2 |
C |
T |
8: 118,282,843 (GRCm39) |
T108M |
probably damaging |
Het |
Pon2 |
G |
A |
6: 5,267,059 (GRCm39) |
|
probably benign |
Het |
Ppef2 |
A |
T |
5: 92,400,952 (GRCm39) |
|
probably benign |
Het |
Pramel21 |
G |
T |
4: 143,342,726 (GRCm39) |
V278F |
probably benign |
Het |
Ptpn22 |
A |
G |
3: 103,767,771 (GRCm39) |
K18E |
probably damaging |
Het |
Pum2 |
C |
T |
12: 8,771,736 (GRCm39) |
Q360* |
probably null |
Het |
Rab10 |
A |
C |
12: 3,302,723 (GRCm39) |
|
probably null |
Het |
Ranbp2 |
T |
G |
10: 58,303,254 (GRCm39) |
S809A |
possibly damaging |
Het |
Rbms2 |
A |
G |
10: 127,969,539 (GRCm39) |
V348A |
probably benign |
Het |
Rpl14 |
C |
A |
9: 120,403,428 (GRCm39) |
|
probably benign |
Het |
Rplp0 |
A |
G |
5: 115,697,931 (GRCm39) |
Y13C |
possibly damaging |
Het |
Ryr1 |
A |
G |
7: 28,703,218 (GRCm39) |
|
probably benign |
Het |
Sac3d1 |
T |
C |
19: 6,168,324 (GRCm39) |
E98G |
probably damaging |
Het |
Scn10a |
T |
A |
9: 119,453,166 (GRCm39) |
D1242V |
probably damaging |
Het |
Scnn1b |
T |
C |
7: 121,498,681 (GRCm39) |
Y74H |
probably damaging |
Het |
Serpinb3a |
C |
T |
1: 106,975,212 (GRCm39) |
W198* |
probably null |
Het |
Sf3b4 |
C |
A |
3: 96,081,017 (GRCm39) |
D108E |
probably damaging |
Het |
Shprh |
T |
C |
10: 11,032,935 (GRCm39) |
V307A |
probably damaging |
Het |
Slc2a2 |
A |
G |
3: 28,781,426 (GRCm39) |
D458G |
probably benign |
Het |
Strc |
T |
C |
2: 121,210,014 (GRCm39) |
D103G |
probably damaging |
Het |
Synrg |
T |
C |
11: 83,910,369 (GRCm39) |
I923T |
probably benign |
Het |
Tango6 |
G |
T |
8: 107,462,314 (GRCm39) |
|
probably benign |
Het |
Tas2r106 |
A |
G |
6: 131,655,539 (GRCm39) |
L104P |
probably damaging |
Het |
Tat |
C |
T |
8: 110,718,316 (GRCm39) |
P67L |
probably damaging |
Het |
Tln2 |
A |
C |
9: 67,262,479 (GRCm39) |
S593A |
probably benign |
Het |
Tmem94 |
A |
G |
11: 115,685,607 (GRCm39) |
|
probably null |
Het |
Tppp3 |
G |
A |
8: 106,194,804 (GRCm39) |
A109V |
probably benign |
Het |
Trank1 |
T |
C |
9: 111,220,361 (GRCm39) |
F2366S |
probably benign |
Het |
Trpc5 |
T |
A |
X: 143,264,392 (GRCm39) |
Y155F |
probably damaging |
Het |
Trpv1 |
A |
G |
11: 73,151,268 (GRCm39) |
T451A |
probably benign |
Het |
Ttc9 |
C |
A |
12: 81,678,423 (GRCm39) |
A82E |
probably damaging |
Het |
Ttll11 |
T |
A |
2: 35,834,886 (GRCm39) |
N180I |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,566,743 (GRCm39) |
N28050S |
possibly damaging |
Het |
Vmn2r73 |
G |
T |
7: 85,522,140 (GRCm39) |
H66Q |
probably benign |
Het |
Vmn2r92 |
C |
T |
17: 18,388,219 (GRCm39) |
A408V |
probably damaging |
Het |
Wnt3 |
G |
A |
11: 103,703,141 (GRCm39) |
C208Y |
probably damaging |
Het |
Zfp521 |
C |
A |
18: 13,978,325 (GRCm39) |
C696F |
probably damaging |
Het |
Zfp521 |
T |
C |
18: 13,979,927 (GRCm39) |
D162G |
probably damaging |
Het |
Zfp869 |
A |
T |
8: 70,159,054 (GRCm39) |
H506Q |
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 |
119,333,946 (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 |
|
|
R8893:Rnf213
|
UTSW |
11 |
119,333,868 (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 |
|
|
|