Other mutations in this stock |
Total: 139 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931403M11Rik |
C |
A |
14: 24,671,419 (GRCm39) |
|
noncoding transcript |
Het |
Abca7 |
A |
G |
10: 79,838,562 (GRCm39) |
K612R |
probably damaging |
Het |
Adamtsl3 |
T |
C |
7: 82,223,822 (GRCm39) |
V275A |
possibly damaging |
Het |
Afg3l1 |
G |
A |
8: 124,215,065 (GRCm39) |
|
probably null |
Het |
Ajm1 |
G |
A |
2: 25,469,759 (GRCm39) |
R51C |
possibly damaging |
Het |
Alcam |
T |
A |
16: 52,089,176 (GRCm39) |
H508L |
probably benign |
Het |
Ankrd45 |
G |
A |
1: 160,982,942 (GRCm39) |
R151H |
probably damaging |
Het |
Aqr |
G |
A |
2: 113,980,990 (GRCm39) |
L264F |
probably damaging |
Het |
Arfgef2 |
G |
A |
2: 166,677,533 (GRCm39) |
A53T |
probably damaging |
Het |
Arhgap30 |
A |
G |
1: 171,236,880 (GRCm39) |
T1085A |
probably benign |
Het |
Atp10a |
T |
C |
7: 58,435,055 (GRCm39) |
V314A |
probably damaging |
Het |
Btbd17 |
T |
A |
11: 114,684,917 (GRCm39) |
T41S |
possibly damaging |
Het |
Cacna1c |
T |
C |
6: 118,728,400 (GRCm39) |
N378S |
probably damaging |
Het |
Camsap1 |
G |
T |
2: 25,825,562 (GRCm39) |
Q1375K |
probably benign |
Het |
Catsper2 |
G |
T |
2: 121,227,604 (GRCm39) |
|
probably null |
Het |
Cblif |
A |
G |
19: 11,729,583 (GRCm39) |
T181A |
probably benign |
Het |
Ccar1 |
A |
G |
10: 62,588,997 (GRCm39) |
S829P |
unknown |
Het |
Ccdc180 |
T |
C |
4: 45,909,308 (GRCm39) |
L492P |
probably damaging |
Het |
Ccser2 |
A |
T |
14: 36,662,343 (GRCm39) |
N280K |
probably damaging |
Het |
Cd37 |
T |
C |
7: 44,883,359 (GRCm39) |
D271G |
probably damaging |
Het |
Cdcp1 |
G |
A |
9: 123,011,194 (GRCm39) |
|
probably benign |
Het |
Cemip2 |
T |
C |
19: 21,833,528 (GRCm39) |
V1322A |
probably benign |
Het |
Cep85 |
T |
A |
4: 133,892,062 (GRCm39) |
|
probably benign |
Het |
Cfi |
C |
T |
3: 129,666,726 (GRCm39) |
P483L |
probably damaging |
Het |
Csmd1 |
A |
G |
8: 15,945,674 (GRCm39) |
|
probably benign |
Het |
Cytl1 |
G |
T |
5: 37,892,918 (GRCm39) |
L9F |
unknown |
Het |
Defb26 |
T |
C |
2: 152,350,085 (GRCm39) |
E65G |
possibly damaging |
Het |
Degs1 |
G |
A |
1: 182,104,370 (GRCm39) |
T305I |
probably damaging |
Het |
Dnttip2 |
T |
G |
3: 122,070,241 (GRCm39) |
C485W |
probably damaging |
Het |
Ecel1 |
G |
A |
1: 87,076,449 (GRCm39) |
|
probably benign |
Het |
Edrf1 |
G |
T |
7: 133,260,339 (GRCm39) |
M83I |
probably damaging |
Het |
Elmo2 |
A |
T |
2: 165,137,209 (GRCm39) |
C562S |
probably benign |
Het |
Etl4 |
T |
A |
2: 20,344,922 (GRCm39) |
|
probably null |
Het |
F2r |
A |
C |
13: 95,740,905 (GRCm39) |
V210G |
probably damaging |
Het |
Fam171a1 |
T |
A |
2: 3,224,546 (GRCm39) |
V179E |
probably damaging |
Het |
Fmod |
G |
T |
1: 133,967,977 (GRCm39) |
V6F |
possibly damaging |
Het |
Foxr2 |
A |
G |
X: 151,913,312 (GRCm39) |
Q61R |
probably damaging |
Het |
Gabra4 |
G |
A |
5: 71,729,546 (GRCm39) |
H76Y |
probably benign |
Het |
Gck |
A |
T |
11: 5,859,150 (GRCm39) |
M139K |
possibly damaging |
Het |
Gm10192 |
C |
G |
4: 97,071,345 (GRCm39) |
S20T |
probably null |
Het |
Gm44501 |
T |
C |
17: 40,887,515 (GRCm39) |
L11P |
unknown |
Het |
Gm572 |
T |
C |
4: 148,751,302 (GRCm39) |
|
probably null |
Het |
Gnas |
A |
G |
2: 174,139,882 (GRCm39) |
K17R |
possibly damaging |
Het |
Grm2 |
T |
A |
9: 106,527,865 (GRCm39) |
S340C |
probably damaging |
Het |
Gsc |
T |
A |
12: 104,438,274 (GRCm39) |
H198L |
probably damaging |
Het |
H2-Q3 |
A |
T |
17: 35,578,424 (GRCm39) |
|
noncoding transcript |
Het |
H4c1 |
T |
C |
13: 23,944,935 (GRCm39) |
D69G |
probably damaging |
Het |
Hivep3 |
A |
G |
4: 119,980,131 (GRCm39) |
E1723G |
probably damaging |
Het |
Hk3 |
A |
T |
13: 55,154,405 (GRCm39) |
L757Q |
probably damaging |
Het |
Homer2 |
A |
T |
7: 81,299,311 (GRCm39) |
D51E |
probably benign |
Het |
Ier3ip1 |
T |
A |
18: 77,027,227 (GRCm39) |
|
probably benign |
Het |
Itch |
T |
A |
2: 155,059,897 (GRCm39) |
|
probably null |
Het |
Kalrn |
T |
A |
16: 33,991,700 (GRCm39) |
Q974L |
probably damaging |
Het |
Kirrel3 |
G |
T |
9: 34,924,601 (GRCm39) |
G296W |
probably damaging |
Het |
Klhl17 |
A |
G |
4: 156,315,082 (GRCm39) |
V525A |
probably benign |
Het |
Klhl9 |
T |
C |
4: 88,640,182 (GRCm39) |
K20E |
probably benign |
Het |
Kmt2a |
G |
T |
9: 44,732,977 (GRCm39) |
|
probably benign |
Het |
Krt17 |
C |
A |
11: 100,147,305 (GRCm39) |
V409L |
probably benign |
Het |
Lmx1b |
T |
C |
2: 33,454,802 (GRCm39) |
N322S |
probably benign |
Het |
Lrrc63 |
G |
C |
14: 75,363,406 (GRCm39) |
P242A |
probably benign |
Het |
Ltk |
T |
C |
2: 119,583,708 (GRCm39) |
N256D |
probably damaging |
Het |
Map3k19 |
T |
A |
1: 127,745,470 (GRCm39) |
E1328V |
probably damaging |
Het |
Map4k2 |
C |
T |
19: 6,394,033 (GRCm39) |
A280V |
probably benign |
Het |
Micall1 |
C |
T |
15: 79,016,048 (GRCm39) |
R802* |
probably null |
Het |
Mmp14 |
A |
G |
14: 54,673,662 (GRCm39) |
R109G |
probably damaging |
Het |
Mmp27 |
A |
T |
9: 7,581,369 (GRCm39) |
H544L |
probably benign |
Het |
Mpeg1 |
A |
G |
19: 12,440,434 (GRCm39) |
T631A |
probably damaging |
Het |
Mpnd |
A |
G |
17: 56,318,641 (GRCm39) |
M217V |
probably benign |
Het |
Mrc2 |
T |
C |
11: 105,232,034 (GRCm39) |
V862A |
probably damaging |
Het |
Mug2 |
T |
A |
6: 122,058,154 (GRCm39) |
S1239T |
probably damaging |
Het |
Myb |
T |
A |
10: 21,002,137 (GRCm39) |
M616L |
probably benign |
Het |
Myo18b |
A |
T |
5: 113,022,346 (GRCm39) |
|
probably benign |
Het |
Myo1c |
C |
A |
11: 75,560,053 (GRCm39) |
T703N |
probably damaging |
Het |
Myt1l |
T |
G |
12: 29,936,138 (GRCm39) |
C909G |
unknown |
Het |
Nbea |
T |
C |
3: 55,912,776 (GRCm39) |
S1004G |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,186,319 (GRCm39) |
N918D |
probably benign |
Het |
Nrtn |
T |
C |
17: 57,058,636 (GRCm39) |
T122A |
probably damaging |
Het |
Nsd3 |
A |
T |
8: 26,188,939 (GRCm39) |
S1042C |
probably damaging |
Het |
Ntmt2 |
A |
T |
1: 163,530,633 (GRCm39) |
C269S |
probably benign |
Het |
Nvl |
A |
G |
1: 180,945,191 (GRCm39) |
L461S |
probably damaging |
Het |
Onecut2 |
A |
T |
18: 64,473,998 (GRCm39) |
H183L |
possibly damaging |
Het |
Or13p5 |
A |
C |
4: 118,591,885 (GRCm39) |
H53P |
probably benign |
Het |
Or2h2 |
G |
A |
17: 37,396,343 (GRCm39) |
T238I |
probably damaging |
Het |
Or4d10 |
C |
G |
19: 12,051,679 (GRCm39) |
G106R |
probably damaging |
Het |
Or52e4 |
A |
G |
7: 104,705,689 (GRCm39) |
T79A |
possibly damaging |
Het |
Or5c1 |
T |
G |
2: 37,222,601 (GRCm39) |
F281V |
probably damaging |
Het |
Or6c1b |
A |
C |
10: 129,273,248 (GRCm39) |
D189A |
possibly damaging |
Het |
Or6z5 |
A |
T |
7: 6,477,612 (GRCm39) |
I168F |
probably damaging |
Het |
Pcdhb21 |
G |
T |
18: 37,648,130 (GRCm39) |
V420F |
possibly damaging |
Het |
Pcdhb9 |
G |
A |
18: 37,536,286 (GRCm39) |
G760D |
probably benign |
Het |
Pglyrp2 |
G |
A |
17: 32,637,771 (GRCm39) |
P86S |
probably benign |
Het |
Phyhip |
T |
A |
14: 70,704,765 (GRCm39) |
V328E |
probably damaging |
Het |
Pitpnb |
A |
T |
5: 111,530,862 (GRCm39) |
K218N |
possibly damaging |
Het |
Pitrm1 |
A |
G |
13: 6,628,596 (GRCm39) |
D963G |
probably damaging |
Het |
Pmfbp1 |
A |
G |
8: 110,258,792 (GRCm39) |
Y699C |
probably damaging |
Het |
Pmpcb |
T |
A |
5: 21,945,660 (GRCm39) |
|
probably benign |
Het |
Polg |
A |
T |
7: 79,114,353 (GRCm39) |
W203R |
probably damaging |
Het |
Pramel22 |
A |
G |
4: 143,380,971 (GRCm39) |
S351P |
probably benign |
Het |
Prss41 |
A |
T |
17: 24,055,977 (GRCm39) |
M252K |
probably benign |
Het |
Prss46 |
A |
T |
9: 110,673,618 (GRCm39) |
M1L |
possibly damaging |
Het |
Rimklb |
T |
C |
6: 122,441,051 (GRCm39) |
|
probably null |
Het |
Rngtt |
T |
C |
4: 33,500,335 (GRCm39) |
I556T |
unknown |
Het |
Rock1 |
A |
C |
18: 10,122,698 (GRCm39) |
D374E |
probably benign |
Het |
Rspry1 |
C |
A |
8: 95,385,417 (GRCm39) |
H450N |
probably benign |
Het |
Rusc2 |
T |
C |
4: 43,423,942 (GRCm39) |
V1032A |
probably damaging |
Het |
Sacs |
A |
G |
14: 61,449,647 (GRCm39) |
R3898G |
probably damaging |
Het |
Scnn1b |
A |
T |
7: 121,502,110 (GRCm39) |
H256L |
probably benign |
Het |
Sh3gl2 |
T |
A |
4: 85,297,494 (GRCm39) |
H157Q |
probably benign |
Het |
Sipa1l1 |
C |
A |
12: 82,389,107 (GRCm39) |
S444R |
probably damaging |
Het |
Sntg1 |
T |
A |
1: 8,433,818 (GRCm39) |
I478F |
probably damaging |
Het |
Spata31e2 |
A |
G |
1: 26,722,628 (GRCm39) |
Y851H |
probably benign |
Het |
Sptb |
G |
T |
12: 76,655,811 (GRCm39) |
L1424M |
probably benign |
Het |
Sry |
T |
A |
Y: 2,663,105 (GRCm39) |
H185L |
unknown |
Het |
Stox2 |
T |
G |
8: 47,656,198 (GRCm39) |
T93P |
probably damaging |
Het |
Tatdn2 |
T |
A |
6: 113,681,566 (GRCm39) |
F472Y |
possibly damaging |
Het |
Tefm |
A |
T |
11: 80,031,185 (GRCm39) |
V17D |
possibly damaging |
Het |
Tekt2 |
G |
T |
4: 126,218,460 (GRCm39) |
T70N |
probably benign |
Het |
Ticam1 |
T |
C |
17: 56,578,642 (GRCm39) |
D151G |
probably damaging |
Het |
Tmem63c |
A |
G |
12: 87,136,139 (GRCm39) |
E785G |
probably damaging |
Het |
Tnmd |
A |
T |
X: 132,765,551 (GRCm39) |
N219I |
probably benign |
Het |
Ttc14 |
T |
A |
3: 33,861,024 (GRCm39) |
L407* |
probably null |
Het |
Ttll7 |
T |
C |
3: 146,599,932 (GRCm39) |
M1T |
probably null |
Het |
Ttn |
T |
A |
2: 76,746,835 (GRCm39) |
|
probably null |
Het |
Uchl1 |
T |
C |
5: 66,833,780 (GRCm39) |
M12T |
probably benign |
Het |
Uggt2 |
A |
T |
14: 119,315,062 (GRCm39) |
|
probably null |
Het |
Uggt2 |
T |
C |
14: 119,286,665 (GRCm39) |
T224A |
probably damaging |
Het |
Umodl1 |
A |
G |
17: 31,218,175 (GRCm39) |
E1254G |
probably damaging |
Het |
Unc5d |
A |
G |
8: 29,156,927 (GRCm39) |
F773L |
probably benign |
Het |
Unc80 |
C |
A |
1: 66,683,606 (GRCm39) |
P2216Q |
probably damaging |
Het |
Usp40 |
T |
A |
1: 87,913,923 (GRCm39) |
|
probably null |
Het |
Vmn1r117 |
A |
T |
7: 20,617,421 (GRCm39) |
M209K |
probably damaging |
Het |
Vmn2r44 |
A |
T |
7: 8,380,985 (GRCm39) |
W303R |
probably benign |
Het |
Wnk2 |
G |
A |
13: 49,224,478 (GRCm39) |
R268C |
probably damaging |
Het |
Wnt2 |
T |
C |
6: 18,023,125 (GRCm39) |
K175E |
possibly damaging |
Het |
Xkr6 |
T |
C |
14: 64,056,953 (GRCm39) |
V288A |
unknown |
Het |
Zfp125 |
A |
G |
12: 20,950,459 (GRCm39) |
|
noncoding transcript |
Het |
Zfp512b |
A |
C |
2: 181,228,856 (GRCm39) |
V703G |
probably damaging |
Het |
Zglp1 |
A |
T |
9: 20,973,957 (GRCm39) |
I243N |
probably benign |
Het |
Zgpat |
T |
C |
2: 181,020,651 (GRCm39) |
S275P |
probably benign |
Het |
|
Other mutations in Bdp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Bdp1
|
APN |
13 |
100,235,018 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00096:Bdp1
|
APN |
13 |
100,197,373 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL00160:Bdp1
|
APN |
13 |
100,197,706 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00924:Bdp1
|
APN |
13 |
100,234,087 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01337:Bdp1
|
APN |
13 |
100,192,700 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01344:Bdp1
|
APN |
13 |
100,214,588 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01347:Bdp1
|
APN |
13 |
100,206,711 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL01620:Bdp1
|
APN |
13 |
100,220,713 (GRCm39) |
splice site |
probably benign |
|
IGL01871:Bdp1
|
APN |
13 |
100,202,561 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02008:Bdp1
|
APN |
13 |
100,160,335 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02112:Bdp1
|
APN |
13 |
100,174,308 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02214:Bdp1
|
APN |
13 |
100,178,043 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02236:Bdp1
|
APN |
13 |
100,197,399 (GRCm39) |
missense |
probably benign |
|
IGL02307:Bdp1
|
APN |
13 |
100,229,946 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02364:Bdp1
|
APN |
13 |
100,191,816 (GRCm39) |
splice site |
probably benign |
|
IGL02415:Bdp1
|
APN |
13 |
100,225,916 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02601:Bdp1
|
APN |
13 |
100,235,022 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02605:Bdp1
|
APN |
13 |
100,214,623 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02664:Bdp1
|
APN |
13 |
100,188,047 (GRCm39) |
missense |
probably benign |
0.29 |
IGL02738:Bdp1
|
APN |
13 |
100,187,861 (GRCm39) |
missense |
probably benign |
0.26 |
IGL02754:Bdp1
|
APN |
13 |
100,197,481 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02967:Bdp1
|
APN |
13 |
100,178,778 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02974:Bdp1
|
APN |
13 |
100,191,800 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03156:Bdp1
|
APN |
13 |
100,197,544 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03166:Bdp1
|
APN |
13 |
100,172,308 (GRCm39) |
missense |
probably benign |
0.28 |
IGL03232:Bdp1
|
APN |
13 |
100,187,989 (GRCm39) |
missense |
probably damaging |
1.00 |
D3080:Bdp1
|
UTSW |
13 |
100,160,129 (GRCm39) |
missense |
probably benign |
0.02 |
R0115:Bdp1
|
UTSW |
13 |
100,177,962 (GRCm39) |
missense |
probably benign |
0.28 |
R0481:Bdp1
|
UTSW |
13 |
100,177,962 (GRCm39) |
missense |
probably benign |
0.28 |
R0619:Bdp1
|
UTSW |
13 |
100,174,366 (GRCm39) |
missense |
probably benign |
0.00 |
R0730:Bdp1
|
UTSW |
13 |
100,195,459 (GRCm39) |
splice site |
probably benign |
|
R0744:Bdp1
|
UTSW |
13 |
100,172,333 (GRCm39) |
missense |
probably benign |
0.01 |
R0833:Bdp1
|
UTSW |
13 |
100,172,333 (GRCm39) |
missense |
probably benign |
0.01 |
R1307:Bdp1
|
UTSW |
13 |
100,186,271 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1325:Bdp1
|
UTSW |
13 |
100,235,516 (GRCm39) |
missense |
probably damaging |
0.97 |
R1346:Bdp1
|
UTSW |
13 |
100,215,263 (GRCm39) |
nonsense |
probably null |
|
R1644:Bdp1
|
UTSW |
13 |
100,197,448 (GRCm39) |
missense |
probably benign |
0.03 |
R1670:Bdp1
|
UTSW |
13 |
100,163,941 (GRCm39) |
critical splice donor site |
probably null |
|
R1836:Bdp1
|
UTSW |
13 |
100,171,653 (GRCm39) |
missense |
probably benign |
|
R1869:Bdp1
|
UTSW |
13 |
100,178,709 (GRCm39) |
missense |
probably damaging |
0.99 |
R1920:Bdp1
|
UTSW |
13 |
100,235,097 (GRCm39) |
missense |
probably benign |
0.30 |
R1944:Bdp1
|
UTSW |
13 |
100,210,889 (GRCm39) |
splice site |
probably null |
|
R2030:Bdp1
|
UTSW |
13 |
100,197,697 (GRCm39) |
missense |
probably benign |
0.00 |
R2069:Bdp1
|
UTSW |
13 |
100,187,496 (GRCm39) |
missense |
probably benign |
0.00 |
R2180:Bdp1
|
UTSW |
13 |
100,197,913 (GRCm39) |
small insertion |
probably benign |
|
R2263:Bdp1
|
UTSW |
13 |
100,202,545 (GRCm39) |
missense |
probably damaging |
0.96 |
R2277:Bdp1
|
UTSW |
13 |
100,197,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R2277:Bdp1
|
UTSW |
13 |
100,197,838 (GRCm39) |
missense |
probably benign |
0.05 |
R2278:Bdp1
|
UTSW |
13 |
100,197,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R2278:Bdp1
|
UTSW |
13 |
100,197,838 (GRCm39) |
missense |
probably benign |
0.05 |
R2336:Bdp1
|
UTSW |
13 |
100,189,510 (GRCm39) |
missense |
probably damaging |
0.99 |
R2380:Bdp1
|
UTSW |
13 |
100,196,878 (GRCm39) |
missense |
probably benign |
0.08 |
R3154:Bdp1
|
UTSW |
13 |
100,186,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R4212:Bdp1
|
UTSW |
13 |
100,196,093 (GRCm39) |
missense |
probably benign |
|
R4322:Bdp1
|
UTSW |
13 |
100,228,731 (GRCm39) |
missense |
probably damaging |
0.97 |
R4414:Bdp1
|
UTSW |
13 |
100,167,369 (GRCm39) |
missense |
probably damaging |
0.99 |
R4415:Bdp1
|
UTSW |
13 |
100,167,369 (GRCm39) |
missense |
probably damaging |
0.99 |
R4764:Bdp1
|
UTSW |
13 |
100,192,775 (GRCm39) |
missense |
probably damaging |
0.99 |
R4766:Bdp1
|
UTSW |
13 |
100,186,376 (GRCm39) |
missense |
probably damaging |
0.96 |
R4914:Bdp1
|
UTSW |
13 |
100,192,844 (GRCm39) |
missense |
probably benign |
0.28 |
R4917:Bdp1
|
UTSW |
13 |
100,191,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R4918:Bdp1
|
UTSW |
13 |
100,191,713 (GRCm39) |
missense |
probably damaging |
0.99 |
R5170:Bdp1
|
UTSW |
13 |
100,167,302 (GRCm39) |
nonsense |
probably null |
|
R5266:Bdp1
|
UTSW |
13 |
100,204,043 (GRCm39) |
missense |
probably benign |
0.33 |
R5312:Bdp1
|
UTSW |
13 |
100,234,109 (GRCm39) |
splice site |
probably null |
|
R5420:Bdp1
|
UTSW |
13 |
100,202,551 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5486:Bdp1
|
UTSW |
13 |
100,235,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R5909:Bdp1
|
UTSW |
13 |
100,228,794 (GRCm39) |
missense |
probably benign |
0.08 |
R5913:Bdp1
|
UTSW |
13 |
100,187,612 (GRCm39) |
missense |
probably benign |
0.41 |
R6018:Bdp1
|
UTSW |
13 |
100,174,732 (GRCm39) |
missense |
probably benign |
0.00 |
R6037:Bdp1
|
UTSW |
13 |
100,163,957 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6037:Bdp1
|
UTSW |
13 |
100,163,957 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6700:Bdp1
|
UTSW |
13 |
100,162,036 (GRCm39) |
missense |
probably benign |
0.00 |
R6969:Bdp1
|
UTSW |
13 |
100,211,039 (GRCm39) |
missense |
probably damaging |
0.97 |
R6972:Bdp1
|
UTSW |
13 |
100,174,269 (GRCm39) |
missense |
probably null |
1.00 |
R6996:Bdp1
|
UTSW |
13 |
100,180,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R7043:Bdp1
|
UTSW |
13 |
100,215,215 (GRCm39) |
missense |
probably benign |
0.03 |
R7060:Bdp1
|
UTSW |
13 |
100,196,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R7105:Bdp1
|
UTSW |
13 |
100,206,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R7155:Bdp1
|
UTSW |
13 |
100,197,659 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7175:Bdp1
|
UTSW |
13 |
100,186,478 (GRCm39) |
missense |
probably damaging |
0.97 |
R7177:Bdp1
|
UTSW |
13 |
100,186,478 (GRCm39) |
missense |
probably damaging |
0.97 |
R7327:Bdp1
|
UTSW |
13 |
100,178,040 (GRCm39) |
missense |
probably damaging |
0.97 |
R7512:Bdp1
|
UTSW |
13 |
100,187,457 (GRCm39) |
missense |
probably benign |
0.03 |
R7562:Bdp1
|
UTSW |
13 |
100,162,049 (GRCm39) |
missense |
probably benign |
0.04 |
R7583:Bdp1
|
UTSW |
13 |
100,186,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R7788:Bdp1
|
UTSW |
13 |
100,191,759 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7842:Bdp1
|
UTSW |
13 |
100,235,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R7850:Bdp1
|
UTSW |
13 |
100,228,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R7904:Bdp1
|
UTSW |
13 |
100,177,944 (GRCm39) |
missense |
probably benign |
0.37 |
R7975:Bdp1
|
UTSW |
13 |
100,156,884 (GRCm39) |
missense |
probably benign |
0.01 |
R7999:Bdp1
|
UTSW |
13 |
100,195,404 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8126:Bdp1
|
UTSW |
13 |
100,192,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R8340:Bdp1
|
UTSW |
13 |
100,202,476 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8414:Bdp1
|
UTSW |
13 |
100,200,985 (GRCm39) |
missense |
probably benign |
0.03 |
R8468:Bdp1
|
UTSW |
13 |
100,197,076 (GRCm39) |
missense |
probably benign |
0.04 |
R8688:Bdp1
|
UTSW |
13 |
100,240,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Bdp1
|
UTSW |
13 |
100,186,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R8976:Bdp1
|
UTSW |
13 |
100,197,407 (GRCm39) |
nonsense |
probably null |
|
R8987:Bdp1
|
UTSW |
13 |
100,204,021 (GRCm39) |
missense |
probably benign |
0.01 |
R9157:Bdp1
|
UTSW |
13 |
100,186,436 (GRCm39) |
missense |
probably benign |
0.40 |
R9437:Bdp1
|
UTSW |
13 |
100,162,158 (GRCm39) |
missense |
probably benign |
0.31 |
R9612:Bdp1
|
UTSW |
13 |
100,214,370 (GRCm39) |
missense |
probably benign |
0.18 |
R9679:Bdp1
|
UTSW |
13 |
100,180,285 (GRCm39) |
missense |
probably damaging |
0.98 |
RF003:Bdp1
|
UTSW |
13 |
100,196,958 (GRCm39) |
missense |
probably benign |
0.31 |
RF003:Bdp1
|
UTSW |
13 |
100,196,957 (GRCm39) |
missense |
probably benign |
0.31 |
Z1177:Bdp1
|
UTSW |
13 |
100,197,904 (GRCm39) |
missense |
probably damaging |
1.00 |
|