Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579F01Rik |
T |
C |
3: 137,882,346 (GRCm39) |
K118R |
possibly damaging |
Het |
Adtrp |
T |
C |
13: 41,920,941 (GRCm39) |
T88A |
probably damaging |
Het |
Afap1l1 |
A |
G |
18: 61,889,976 (GRCm39) |
S87P |
probably benign |
Het |
Ankrd27 |
A |
G |
7: 35,303,125 (GRCm39) |
K196R |
probably benign |
Het |
Apoe |
G |
A |
7: 19,431,005 (GRCm39) |
T79M |
probably damaging |
Het |
Arrdc3 |
T |
A |
13: 81,032,011 (GRCm39) |
Y81* |
probably null |
Het |
Arrdc3 |
T |
A |
13: 81,039,194 (GRCm39) |
I75N |
probably damaging |
Het |
Asah2 |
T |
A |
19: 31,981,131 (GRCm39) |
K629* |
probably null |
Het |
Ass1 |
A |
T |
2: 31,404,831 (GRCm39) |
N371Y |
probably damaging |
Het |
C130074G19Rik |
A |
G |
1: 184,615,119 (GRCm39) |
S24P |
probably benign |
Het |
C87436 |
A |
G |
6: 86,423,265 (GRCm39) |
|
probably benign |
Het |
Calcrl |
T |
C |
2: 84,203,618 (GRCm39) |
D54G |
probably benign |
Het |
Clcn2 |
T |
C |
16: 20,529,140 (GRCm39) |
N367S |
probably null |
Het |
Cnot1 |
G |
T |
8: 96,487,969 (GRCm39) |
D562E |
probably damaging |
Het |
Commd6 |
G |
A |
14: 101,877,709 (GRCm39) |
|
probably benign |
Het |
Cox6a2 |
G |
A |
7: 127,805,212 (GRCm39) |
|
probably benign |
Het |
Cp |
T |
A |
3: 20,022,287 (GRCm39) |
Y230N |
probably damaging |
Het |
Dclre1c |
T |
C |
2: 3,439,032 (GRCm39) |
V64A |
probably damaging |
Het |
Eng |
T |
C |
2: 32,567,692 (GRCm39) |
V110A |
probably damaging |
Het |
Esyt3 |
T |
C |
9: 99,220,860 (GRCm39) |
I114M |
possibly damaging |
Het |
Fam83h |
A |
T |
15: 75,875,811 (GRCm39) |
Y509N |
probably damaging |
Het |
Fat2 |
A |
T |
11: 55,202,075 (GRCm39) |
L333H |
probably damaging |
Het |
Fbxo21 |
A |
G |
5: 118,146,078 (GRCm39) |
N567S |
possibly damaging |
Het |
Fcsk |
T |
C |
8: 111,610,865 (GRCm39) |
|
probably benign |
Het |
Fn1 |
A |
T |
1: 71,634,879 (GRCm39) |
L1964Q |
probably damaging |
Het |
Gorasp1 |
G |
T |
9: 119,757,312 (GRCm39) |
S353R |
possibly damaging |
Het |
Grk2 |
C |
T |
19: 4,337,262 (GRCm39) |
E646K |
probably damaging |
Het |
Hoxc11 |
T |
C |
15: 102,863,397 (GRCm39) |
V146A |
probably damaging |
Het |
Igf2bp2 |
T |
C |
16: 21,894,841 (GRCm39) |
T301A |
probably benign |
Het |
Il11 |
T |
C |
7: 4,776,658 (GRCm39) |
S111G |
probably benign |
Het |
Ist1 |
A |
T |
8: 110,403,418 (GRCm39) |
I273K |
probably benign |
Het |
Kdm2b |
G |
A |
5: 123,019,806 (GRCm39) |
S738L |
probably benign |
Het |
Lrp2 |
T |
A |
2: 69,346,895 (GRCm39) |
N784Y |
probably benign |
Het |
Lrp6 |
T |
C |
6: 134,462,716 (GRCm39) |
E648G |
probably damaging |
Het |
Mapk15 |
G |
A |
15: 75,870,103 (GRCm39) |
E408K |
probably benign |
Het |
Mdn1 |
T |
A |
4: 32,718,317 (GRCm39) |
F2191I |
possibly damaging |
Het |
Metrn |
C |
A |
17: 26,015,479 (GRCm39) |
V79F |
possibly damaging |
Het |
Mtbp |
T |
A |
15: 55,449,889 (GRCm39) |
|
probably benign |
Het |
Myh11 |
C |
A |
16: 14,041,883 (GRCm39) |
Q720H |
probably damaging |
Het |
Myo3a |
T |
A |
2: 22,469,753 (GRCm39) |
I508N |
probably damaging |
Het |
Nat9 |
A |
T |
11: 115,075,941 (GRCm39) |
Y27N |
probably damaging |
Het |
Ncapg2 |
T |
C |
12: 116,393,455 (GRCm39) |
F553S |
probably damaging |
Het |
Nipsnap3b |
T |
A |
4: 53,015,112 (GRCm39) |
L53Q |
probably damaging |
Het |
Nlrp3 |
A |
T |
11: 59,449,274 (GRCm39) |
H852L |
probably benign |
Het |
Or2d3b |
A |
G |
7: 106,514,226 (GRCm39) |
I274V |
probably benign |
Het |
Or2t6 |
T |
A |
14: 14,176,092 (GRCm38) |
|
probably benign |
Het |
Or4a78 |
T |
A |
2: 89,497,428 (GRCm39) |
K267N |
probably damaging |
Het |
Or52e3 |
A |
T |
7: 102,869,558 (GRCm39) |
D211V |
probably damaging |
Het |
Or52e3 |
G |
A |
7: 102,869,584 (GRCm39) |
A220T |
probably benign |
Het |
Or5b122 |
A |
G |
19: 13,563,240 (GRCm39) |
I191V |
probably benign |
Het |
Pax9 |
A |
G |
12: 56,756,528 (GRCm39) |
T289A |
probably benign |
Het |
Pcyt2 |
A |
T |
11: 120,506,695 (GRCm39) |
I53N |
possibly damaging |
Het |
Pdlim4 |
C |
T |
11: 53,945,875 (GRCm39) |
V327M |
probably damaging |
Het |
Pdzph1 |
T |
A |
17: 59,229,756 (GRCm39) |
|
probably benign |
Het |
Plekhm2 |
C |
T |
4: 141,369,704 (GRCm39) |
|
probably benign |
Het |
Ppt1 |
T |
C |
4: 122,742,216 (GRCm39) |
|
probably benign |
Het |
Prdm1 |
C |
T |
10: 44,317,675 (GRCm39) |
E398K |
probably damaging |
Het |
Prep |
T |
C |
10: 44,991,174 (GRCm39) |
V280A |
probably benign |
Het |
Prkdc |
T |
A |
16: 15,526,565 (GRCm39) |
|
probably benign |
Het |
Proser3 |
G |
A |
7: 30,239,563 (GRCm39) |
R514C |
probably damaging |
Het |
Ptk7 |
G |
A |
17: 46,883,688 (GRCm39) |
|
probably benign |
Het |
Rbm45 |
T |
C |
2: 76,208,742 (GRCm39) |
Y293H |
probably damaging |
Het |
Sdk2 |
A |
G |
11: 113,747,581 (GRCm39) |
L643P |
probably damaging |
Het |
Sec24d |
C |
A |
3: 123,144,525 (GRCm39) |
|
probably benign |
Het |
Sh2d3c |
C |
G |
2: 32,643,033 (GRCm39) |
H587D |
probably damaging |
Het |
Slc1a1 |
G |
A |
19: 28,878,884 (GRCm39) |
G208S |
probably benign |
Het |
Slc35b4 |
A |
T |
6: 34,135,452 (GRCm39) |
Y287N |
probably damaging |
Het |
Slc46a2 |
T |
A |
4: 59,914,544 (GRCm39) |
L126F |
probably damaging |
Het |
Slc4a8 |
T |
C |
15: 100,698,374 (GRCm39) |
M621T |
possibly damaging |
Het |
Slc9b2 |
T |
A |
3: 135,042,269 (GRCm39) |
V516D |
possibly damaging |
Het |
Slco1a6 |
T |
A |
6: 142,102,948 (GRCm39) |
|
probably benign |
Het |
Sncg |
C |
T |
14: 34,096,495 (GRCm39) |
V15I |
probably benign |
Het |
Srgap2 |
T |
C |
1: 131,283,302 (GRCm39) |
T260A |
probably damaging |
Het |
Stk10 |
T |
A |
11: 32,537,305 (GRCm39) |
|
probably benign |
Het |
Taf5 |
A |
G |
19: 47,064,301 (GRCm39) |
S415G |
possibly damaging |
Het |
Tdp1 |
C |
T |
12: 99,921,217 (GRCm39) |
|
probably benign |
Het |
Tdp2 |
T |
G |
13: 25,025,333 (GRCm39) |
|
probably null |
Het |
Tgfbi |
T |
A |
13: 56,777,587 (GRCm39) |
I357N |
probably benign |
Het |
Tmem116 |
A |
G |
5: 121,633,159 (GRCm39) |
T178A |
probably damaging |
Het |
Tnrc6a |
G |
A |
7: 122,769,617 (GRCm39) |
R469H |
probably benign |
Het |
Top2a |
A |
T |
11: 98,893,729 (GRCm39) |
L1055* |
probably null |
Het |
Tox |
T |
A |
4: 6,842,411 (GRCm39) |
M40L |
probably benign |
Het |
Trib2 |
A |
T |
12: 15,859,930 (GRCm39) |
H110Q |
probably benign |
Het |
Trpa1 |
A |
G |
1: 14,973,439 (GRCm39) |
I293T |
possibly damaging |
Het |
Trpv2 |
A |
G |
11: 62,481,086 (GRCm39) |
Y395C |
probably damaging |
Het |
Ubn2 |
T |
A |
6: 38,411,535 (GRCm39) |
|
probably null |
Het |
Ubr4 |
C |
T |
4: 139,157,487 (GRCm39) |
T2348M |
probably damaging |
Het |
Ubxn4 |
G |
A |
1: 128,190,641 (GRCm39) |
E256K |
probably benign |
Het |
Vmn1r33 |
C |
A |
6: 66,589,510 (GRCm39) |
G15* |
probably null |
Het |
Vmn1r37 |
T |
A |
6: 66,708,769 (GRCm39) |
S95T |
probably benign |
Het |
Vmn2r57 |
A |
G |
7: 41,050,076 (GRCm39) |
C558R |
probably damaging |
Het |
Vnn1 |
T |
C |
10: 23,774,500 (GRCm39) |
|
probably null |
Het |
Vps13c |
T |
C |
9: 67,826,544 (GRCm39) |
V1395A |
probably benign |
Het |
Vwa7 |
A |
G |
17: 35,238,781 (GRCm39) |
I290V |
probably benign |
Het |
Wdr93 |
A |
G |
7: 79,408,221 (GRCm39) |
E234G |
probably damaging |
Het |
Zfp385b |
A |
T |
2: 77,246,291 (GRCm39) |
S245R |
probably benign |
Het |
Zfp942 |
A |
T |
17: 22,147,319 (GRCm39) |
C437S |
probably damaging |
Het |
Zfyve9 |
T |
A |
4: 108,575,902 (GRCm39) |
E393V |
possibly 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 |
|
|
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 |
|
|
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 |
|
|
|