Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
T |
G |
15: 64,626,735 (GRCm39) |
|
probably null |
Het |
Adgrv1 |
A |
G |
13: 81,705,200 (GRCm39) |
F1537L |
probably damaging |
Het |
Aggf1 |
T |
C |
13: 95,501,231 (GRCm39) |
S384G |
probably benign |
Het |
Anxa8 |
A |
T |
14: 33,816,722 (GRCm39) |
D204V |
possibly damaging |
Het |
Asap3 |
A |
T |
4: 135,954,883 (GRCm39) |
E71V |
possibly damaging |
Het |
BC024139 |
T |
C |
15: 76,003,946 (GRCm39) |
*773W |
probably null |
Het |
Bckdhb |
T |
C |
9: 83,835,814 (GRCm39) |
V106A |
possibly damaging |
Het |
Cep250 |
A |
G |
2: 155,823,379 (GRCm39) |
D1010G |
probably benign |
Het |
Chrd |
T |
A |
16: 20,553,486 (GRCm39) |
L243Q |
probably damaging |
Het |
Cib2 |
G |
T |
9: 54,457,175 (GRCm39) |
L30I |
possibly damaging |
Het |
Cpsf7 |
T |
A |
19: 10,510,248 (GRCm39) |
L113* |
probably null |
Het |
Cubn |
T |
A |
2: 13,449,840 (GRCm39) |
I895L |
probably benign |
Het |
Cyp24a1 |
C |
A |
2: 170,329,899 (GRCm39) |
R351I |
probably benign |
Het |
Cyp2a12 |
A |
T |
7: 26,733,581 (GRCm39) |
D320V |
possibly damaging |
Het |
Dact1 |
C |
G |
12: 71,364,713 (GRCm39) |
P498R |
probably benign |
Het |
Diaph1 |
T |
A |
18: 38,009,436 (GRCm39) |
|
probably null |
Het |
Dnah7a |
A |
T |
1: 53,495,863 (GRCm39) |
I3198N |
probably benign |
Het |
Dop1b |
A |
T |
16: 93,552,373 (GRCm39) |
I271F |
possibly damaging |
Het |
Elp1 |
A |
G |
4: 56,787,939 (GRCm39) |
Y331H |
probably damaging |
Het |
Erich3 |
C |
A |
3: 154,433,074 (GRCm39) |
F349L |
probably damaging |
Het |
Fam187b |
G |
C |
7: 30,688,715 (GRCm39) |
V358L |
probably benign |
Het |
Fat4 |
T |
A |
3: 39,038,088 (GRCm39) |
H3913Q |
probably benign |
Het |
Fbxw7 |
G |
C |
3: 84,865,934 (GRCm39) |
E118D |
probably benign |
Het |
Fgf1 |
A |
G |
18: 38,980,161 (GRCm39) |
I71T |
probably damaging |
Het |
Galnt2 |
C |
G |
8: 125,050,750 (GRCm39) |
P130A |
probably benign |
Het |
H1f10 |
G |
A |
6: 87,958,284 (GRCm39) |
R19C |
probably damaging |
Het |
Hmga2 |
A |
C |
10: 120,311,929 (GRCm39) |
S14A |
possibly damaging |
Het |
Hoxb4 |
C |
T |
11: 96,209,480 (GRCm39) |
|
probably benign |
Het |
Hr |
A |
T |
14: 70,802,814 (GRCm39) |
I756F |
probably damaging |
Het |
Hspa1b |
A |
T |
17: 35,177,161 (GRCm39) |
S275T |
probably benign |
Het |
Kcnh1 |
T |
C |
1: 192,187,597 (GRCm39) |
*99R |
probably null |
Het |
Kit |
C |
A |
5: 75,813,309 (GRCm39) |
L864I |
probably benign |
Het |
Klk14 |
A |
T |
7: 43,343,880 (GRCm39) |
K196* |
probably null |
Het |
Lmod1 |
A |
G |
1: 135,252,905 (GRCm39) |
N53S |
probably damaging |
Het |
Myh13 |
T |
C |
11: 67,246,984 (GRCm39) |
M1235T |
probably benign |
Het |
Neurl3 |
T |
A |
1: 36,307,785 (GRCm39) |
K175* |
probably null |
Het |
Nlgn2 |
T |
A |
11: 69,716,750 (GRCm39) |
K597M |
probably damaging |
Het |
Npdc1 |
T |
C |
2: 25,299,121 (GRCm39) |
M306T |
probably damaging |
Het |
Obscn |
C |
T |
11: 58,958,769 (GRCm39) |
|
probably null |
Het |
Or1p1b |
T |
C |
11: 74,130,522 (GRCm39) |
L44P |
probably damaging |
Het |
Or52m2 |
G |
A |
7: 102,263,693 (GRCm39) |
L168F |
probably damaging |
Het |
Or8b49 |
T |
C |
9: 38,506,201 (GRCm39) |
I228T |
possibly damaging |
Het |
Pbrm1 |
A |
T |
14: 30,806,747 (GRCm39) |
Y1042F |
probably damaging |
Het |
Pclo |
T |
A |
5: 14,727,921 (GRCm39) |
|
probably benign |
Het |
Peg10 |
CATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAGGATC |
CATC |
6: 4,756,431 (GRCm39) |
|
probably benign |
Het |
Phf12 |
C |
T |
11: 77,913,337 (GRCm39) |
Q430* |
probably null |
Het |
Plaat5 |
A |
T |
19: 7,616,861 (GRCm39) |
|
probably benign |
Het |
Pld3 |
C |
T |
7: 27,235,322 (GRCm39) |
R302H |
probably damaging |
Het |
Plekha5 |
T |
C |
6: 140,471,584 (GRCm39) |
S112P |
probably benign |
Het |
Pmfbp1 |
T |
A |
8: 110,256,939 (GRCm39) |
S548T |
possibly damaging |
Het |
Ppa1 |
A |
T |
10: 61,503,382 (GRCm39) |
I220F |
probably damaging |
Het |
Ppp2r3d |
A |
G |
9: 124,439,078 (GRCm38) |
|
probably benign |
Het |
Psmg2 |
A |
T |
18: 67,781,927 (GRCm39) |
E164D |
possibly damaging |
Het |
Rarb |
T |
C |
14: 16,443,824 (GRCm38) |
R155G |
probably damaging |
Het |
Rnf215 |
T |
C |
11: 4,086,609 (GRCm39) |
L162S |
probably damaging |
Het |
Rsf1 |
GGCG |
GGCGACGGCCGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Rtkn2 |
G |
A |
10: 67,862,462 (GRCm39) |
V330M |
probably damaging |
Het |
Slc16a4 |
A |
T |
3: 107,218,814 (GRCm39) |
I472F |
probably benign |
Het |
Snx14 |
T |
C |
9: 88,276,435 (GRCm39) |
N617D |
possibly damaging |
Het |
Spire2 |
T |
C |
8: 124,083,466 (GRCm39) |
V150A |
probably damaging |
Het |
Sptbn1 |
C |
A |
11: 30,064,787 (GRCm39) |
R1904M |
probably damaging |
Het |
Swap70 |
A |
G |
7: 109,880,510 (GRCm39) |
E575G |
possibly damaging |
Het |
Tbxas1 |
A |
T |
6: 38,896,087 (GRCm39) |
M1L |
possibly damaging |
Het |
Tenm3 |
A |
T |
8: 48,709,872 (GRCm39) |
V1688D |
probably damaging |
Het |
Tgfbr3 |
A |
T |
5: 107,297,780 (GRCm39) |
S207T |
probably damaging |
Het |
Timm44 |
A |
G |
8: 4,317,282 (GRCm39) |
F248L |
probably damaging |
Het |
Tmem161a |
T |
C |
8: 70,633,849 (GRCm39) |
L170P |
probably damaging |
Het |
Tmem63a |
A |
T |
1: 180,788,035 (GRCm39) |
Y263F |
possibly damaging |
Het |
Tnfsf9 |
C |
A |
17: 57,412,513 (GRCm39) |
L28I |
probably benign |
Het |
Tph2 |
T |
A |
10: 115,010,011 (GRCm39) |
N183I |
probably benign |
Het |
Ttyh1 |
T |
C |
7: 4,125,528 (GRCm39) |
I60T |
probably damaging |
Het |
Ubn1 |
T |
G |
16: 4,882,411 (GRCm39) |
S48A |
probably damaging |
Het |
Ubr5 |
T |
C |
15: 37,989,842 (GRCm39) |
N2019S |
probably benign |
Het |
Wbp2 |
T |
C |
11: 115,977,736 (GRCm39) |
N6D |
probably benign |
Het |
Wdr59 |
T |
A |
8: 112,185,672 (GRCm39) |
E810V |
possibly damaging |
Het |
Wiz |
T |
C |
17: 32,579,395 (GRCm39) |
D220G |
probably damaging |
Het |
Yipf7 |
A |
G |
5: 69,674,413 (GRCm39) |
L244P |
probably damaging |
Het |
Zdhhc17 |
T |
C |
10: 110,790,972 (GRCm39) |
T366A |
possibly damaging |
Het |
Zfp169 |
A |
T |
13: 48,644,472 (GRCm39) |
|
probably benign |
Het |
Zfp707 |
C |
T |
15: 75,841,572 (GRCm39) |
|
probably benign |
Het |
Zfp788 |
A |
G |
7: 41,298,984 (GRCm39) |
H540R |
probably damaging |
Het |
|
Other mutations in Fryl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00819:Fryl
|
APN |
5 |
73,305,451 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01518:Fryl
|
APN |
5 |
73,244,305 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL01545:Fryl
|
APN |
5 |
73,211,940 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01646:Fryl
|
APN |
5 |
73,179,844 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01938:Fryl
|
APN |
5 |
73,279,707 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01962:Fryl
|
APN |
5 |
73,190,134 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02064:Fryl
|
APN |
5 |
73,282,112 (GRCm39) |
unclassified |
probably benign |
|
IGL02148:Fryl
|
APN |
5 |
73,233,302 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02418:Fryl
|
APN |
5 |
73,267,519 (GRCm39) |
splice site |
probably benign |
|
IGL02431:Fryl
|
APN |
5 |
73,255,651 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02513:Fryl
|
APN |
5 |
73,222,636 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02557:Fryl
|
APN |
5 |
73,255,736 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02625:Fryl
|
APN |
5 |
73,227,220 (GRCm39) |
intron |
probably benign |
|
IGL02642:Fryl
|
APN |
5 |
73,252,809 (GRCm39) |
missense |
probably benign |
|
IGL02657:Fryl
|
APN |
5 |
73,212,203 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02706:Fryl
|
APN |
5 |
73,250,506 (GRCm39) |
missense |
probably benign |
0.45 |
IGL03022:Fryl
|
APN |
5 |
73,216,726 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL03144:Fryl
|
APN |
5 |
73,258,798 (GRCm39) |
missense |
probably null |
0.22 |
IGL03155:Fryl
|
APN |
5 |
73,234,038 (GRCm39) |
missense |
probably benign |
|
IGL03183:Fryl
|
APN |
5 |
73,234,038 (GRCm39) |
missense |
probably benign |
|
IGL03275:Fryl
|
APN |
5 |
73,305,376 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03310:Fryl
|
APN |
5 |
73,293,659 (GRCm39) |
splice site |
probably benign |
|
IGL03341:Fryl
|
APN |
5 |
73,234,038 (GRCm39) |
missense |
probably benign |
|
IGL03343:Fryl
|
APN |
5 |
73,234,038 (GRCm39) |
missense |
probably benign |
|
IGL03350:Fryl
|
APN |
5 |
73,290,649 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03357:Fryl
|
APN |
5 |
73,211,402 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03374:Fryl
|
APN |
5 |
73,267,624 (GRCm39) |
splice site |
probably benign |
|
IGL03375:Fryl
|
APN |
5 |
73,245,792 (GRCm39) |
missense |
possibly damaging |
0.91 |
bedeviled
|
UTSW |
5 |
73,216,843 (GRCm39) |
missense |
probably damaging |
1.00 |
Besotted
|
UTSW |
5 |
73,230,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R0062:Fryl
|
UTSW |
5 |
73,179,621 (GRCm39) |
missense |
probably benign |
0.02 |
R0062:Fryl
|
UTSW |
5 |
73,179,621 (GRCm39) |
missense |
probably benign |
0.02 |
R0308:Fryl
|
UTSW |
5 |
73,198,947 (GRCm39) |
splice site |
probably benign |
|
R0312:Fryl
|
UTSW |
5 |
73,230,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R0415:Fryl
|
UTSW |
5 |
73,255,757 (GRCm39) |
missense |
probably damaging |
0.99 |
R0440:Fryl
|
UTSW |
5 |
73,244,315 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0446:Fryl
|
UTSW |
5 |
73,254,760 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0566:Fryl
|
UTSW |
5 |
73,221,840 (GRCm39) |
splice site |
probably benign |
|
R0567:Fryl
|
UTSW |
5 |
73,222,734 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0606:Fryl
|
UTSW |
5 |
73,282,077 (GRCm39) |
missense |
probably benign |
0.15 |
R0619:Fryl
|
UTSW |
5 |
73,226,074 (GRCm39) |
missense |
probably benign |
0.22 |
R0654:Fryl
|
UTSW |
5 |
73,240,715 (GRCm39) |
missense |
probably benign |
0.17 |
R0658:Fryl
|
UTSW |
5 |
73,222,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R0707:Fryl
|
UTSW |
5 |
73,240,715 (GRCm39) |
missense |
probably benign |
0.17 |
R0744:Fryl
|
UTSW |
5 |
73,246,424 (GRCm39) |
unclassified |
probably benign |
|
R0745:Fryl
|
UTSW |
5 |
73,228,469 (GRCm39) |
missense |
probably damaging |
0.96 |
R0833:Fryl
|
UTSW |
5 |
73,246,424 (GRCm39) |
unclassified |
probably benign |
|
R0885:Fryl
|
UTSW |
5 |
73,246,539 (GRCm39) |
missense |
probably damaging |
0.97 |
R0894:Fryl
|
UTSW |
5 |
73,198,675 (GRCm39) |
splice site |
probably benign |
|
R1076:Fryl
|
UTSW |
5 |
73,282,016 (GRCm39) |
unclassified |
probably benign |
|
R1241:Fryl
|
UTSW |
5 |
73,267,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R1241:Fryl
|
UTSW |
5 |
73,222,268 (GRCm39) |
splice site |
probably benign |
|
R1394:Fryl
|
UTSW |
5 |
73,230,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R1395:Fryl
|
UTSW |
5 |
73,230,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R1608:Fryl
|
UTSW |
5 |
73,232,094 (GRCm39) |
nonsense |
probably null |
|
R1664:Fryl
|
UTSW |
5 |
73,216,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R1745:Fryl
|
UTSW |
5 |
73,190,204 (GRCm39) |
splice site |
probably benign |
|
R1937:Fryl
|
UTSW |
5 |
73,290,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Fryl
|
UTSW |
5 |
73,255,609 (GRCm39) |
missense |
probably benign |
0.18 |
R1993:Fryl
|
UTSW |
5 |
73,265,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R1994:Fryl
|
UTSW |
5 |
73,265,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R2029:Fryl
|
UTSW |
5 |
73,179,465 (GRCm39) |
nonsense |
probably null |
|
R2036:Fryl
|
UTSW |
5 |
73,265,305 (GRCm39) |
critical splice donor site |
probably null |
|
R2036:Fryl
|
UTSW |
5 |
73,179,887 (GRCm39) |
missense |
probably benign |
|
R2088:Fryl
|
UTSW |
5 |
73,222,804 (GRCm39) |
missense |
probably benign |
0.02 |
R2105:Fryl
|
UTSW |
5 |
73,279,642 (GRCm39) |
missense |
probably benign |
|
R2106:Fryl
|
UTSW |
5 |
73,255,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R2186:Fryl
|
UTSW |
5 |
73,222,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R2239:Fryl
|
UTSW |
5 |
73,265,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R2256:Fryl
|
UTSW |
5 |
73,230,187 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2257:Fryl
|
UTSW |
5 |
73,230,187 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2280:Fryl
|
UTSW |
5 |
73,198,707 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2281:Fryl
|
UTSW |
5 |
73,198,707 (GRCm39) |
missense |
possibly damaging |
0.47 |
R2911:Fryl
|
UTSW |
5 |
73,207,799 (GRCm39) |
missense |
probably damaging |
0.99 |
R3019:Fryl
|
UTSW |
5 |
73,240,193 (GRCm39) |
missense |
probably benign |
0.01 |
R3416:Fryl
|
UTSW |
5 |
73,265,417 (GRCm39) |
missense |
possibly damaging |
0.84 |
R3783:Fryl
|
UTSW |
5 |
73,258,819 (GRCm39) |
missense |
probably benign |
|
R3787:Fryl
|
UTSW |
5 |
73,258,819 (GRCm39) |
missense |
probably benign |
|
R3837:Fryl
|
UTSW |
5 |
73,228,608 (GRCm39) |
missense |
probably benign |
0.03 |
R3969:Fryl
|
UTSW |
5 |
73,269,766 (GRCm39) |
missense |
probably damaging |
0.97 |
R4387:Fryl
|
UTSW |
5 |
73,243,903 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4502:Fryl
|
UTSW |
5 |
73,245,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R4658:Fryl
|
UTSW |
5 |
73,238,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R4664:Fryl
|
UTSW |
5 |
73,248,022 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4690:Fryl
|
UTSW |
5 |
73,257,636 (GRCm39) |
missense |
probably benign |
|
R4700:Fryl
|
UTSW |
5 |
73,222,881 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4709:Fryl
|
UTSW |
5 |
73,238,315 (GRCm39) |
missense |
probably benign |
0.03 |
R4807:Fryl
|
UTSW |
5 |
73,198,705 (GRCm39) |
missense |
probably benign |
0.00 |
R4912:Fryl
|
UTSW |
5 |
73,226,125 (GRCm39) |
frame shift |
probably null |
|
R4948:Fryl
|
UTSW |
5 |
73,246,473 (GRCm39) |
missense |
probably benign |
0.08 |
R4959:Fryl
|
UTSW |
5 |
73,192,401 (GRCm39) |
missense |
probably benign |
0.00 |
R5062:Fryl
|
UTSW |
5 |
73,233,236 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5067:Fryl
|
UTSW |
5 |
73,215,098 (GRCm39) |
missense |
probably benign |
0.13 |
R5071:Fryl
|
UTSW |
5 |
73,232,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R5072:Fryl
|
UTSW |
5 |
73,232,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R5073:Fryl
|
UTSW |
5 |
73,232,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R5074:Fryl
|
UTSW |
5 |
73,232,110 (GRCm39) |
missense |
probably damaging |
0.99 |
R5139:Fryl
|
UTSW |
5 |
73,248,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R5172:Fryl
|
UTSW |
5 |
73,259,016 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5187:Fryl
|
UTSW |
5 |
73,243,943 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5272:Fryl
|
UTSW |
5 |
73,222,479 (GRCm39) |
nonsense |
probably null |
|
R5275:Fryl
|
UTSW |
5 |
73,270,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R5295:Fryl
|
UTSW |
5 |
73,270,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R5344:Fryl
|
UTSW |
5 |
73,262,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R5355:Fryl
|
UTSW |
5 |
73,231,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R5716:Fryl
|
UTSW |
5 |
73,257,808 (GRCm39) |
missense |
probably benign |
|
R5778:Fryl
|
UTSW |
5 |
73,230,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R5810:Fryl
|
UTSW |
5 |
73,248,098 (GRCm39) |
missense |
probably benign |
0.06 |
R5934:Fryl
|
UTSW |
5 |
73,248,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R5948:Fryl
|
UTSW |
5 |
73,254,715 (GRCm39) |
critical splice donor site |
probably null |
|
R6005:Fryl
|
UTSW |
5 |
73,240,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R6026:Fryl
|
UTSW |
5 |
73,257,340 (GRCm39) |
missense |
probably benign |
0.04 |
R6045:Fryl
|
UTSW |
5 |
73,275,894 (GRCm39) |
missense |
probably damaging |
0.99 |
R6185:Fryl
|
UTSW |
5 |
73,270,131 (GRCm39) |
missense |
probably benign |
0.43 |
R6247:Fryl
|
UTSW |
5 |
73,222,824 (GRCm39) |
missense |
probably damaging |
0.98 |
R6294:Fryl
|
UTSW |
5 |
73,349,102 (GRCm39) |
intron |
probably benign |
|
R6310:Fryl
|
UTSW |
5 |
73,349,104 (GRCm39) |
intron |
probably benign |
|
R6429:Fryl
|
UTSW |
5 |
73,248,094 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6568:Fryl
|
UTSW |
5 |
73,216,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R6636:Fryl
|
UTSW |
5 |
73,290,655 (GRCm39) |
missense |
probably benign |
0.01 |
R6664:Fryl
|
UTSW |
5 |
73,289,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R6732:Fryl
|
UTSW |
5 |
73,212,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R6750:Fryl
|
UTSW |
5 |
73,179,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R6805:Fryl
|
UTSW |
5 |
73,222,437 (GRCm39) |
missense |
probably benign |
0.03 |
R6855:Fryl
|
UTSW |
5 |
73,216,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R6858:Fryl
|
UTSW |
5 |
73,222,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R6868:Fryl
|
UTSW |
5 |
73,226,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R6898:Fryl
|
UTSW |
5 |
73,179,485 (GRCm39) |
missense |
probably damaging |
0.96 |
R6908:Fryl
|
UTSW |
5 |
73,179,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R6958:Fryl
|
UTSW |
5 |
73,231,272 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6980:Fryl
|
UTSW |
5 |
73,207,773 (GRCm39) |
missense |
probably benign |
0.06 |
R7036:Fryl
|
UTSW |
5 |
73,212,951 (GRCm39) |
missense |
probably benign |
0.03 |
R7065:Fryl
|
UTSW |
5 |
73,248,099 (GRCm39) |
missense |
probably damaging |
0.96 |
R7097:Fryl
|
UTSW |
5 |
73,231,251 (GRCm39) |
missense |
probably benign |
0.31 |
R7171:Fryl
|
UTSW |
5 |
73,279,653 (GRCm39) |
missense |
probably damaging |
0.97 |
R7191:Fryl
|
UTSW |
5 |
73,230,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R7207:Fryl
|
UTSW |
5 |
73,222,438 (GRCm39) |
missense |
probably benign |
|
R7236:Fryl
|
UTSW |
5 |
73,265,821 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7334:Fryl
|
UTSW |
5 |
73,204,839 (GRCm39) |
splice site |
probably null |
|
R7425:Fryl
|
UTSW |
5 |
73,262,091 (GRCm39) |
missense |
probably damaging |
1.00 |
R7452:Fryl
|
UTSW |
5 |
73,181,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R7479:Fryl
|
UTSW |
5 |
73,254,904 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7535:Fryl
|
UTSW |
5 |
73,255,539 (GRCm39) |
missense |
probably benign |
0.15 |
R7538:Fryl
|
UTSW |
5 |
73,180,019 (GRCm39) |
missense |
probably benign |
0.09 |
R7544:Fryl
|
UTSW |
5 |
73,238,382 (GRCm39) |
missense |
probably benign |
|
R7548:Fryl
|
UTSW |
5 |
73,349,105 (GRCm39) |
missense |
unknown |
|
R7565:Fryl
|
UTSW |
5 |
73,191,063 (GRCm39) |
missense |
probably benign |
0.18 |
R7572:Fryl
|
UTSW |
5 |
73,245,739 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7582:Fryl
|
UTSW |
5 |
73,179,843 (GRCm39) |
critical splice donor site |
probably null |
|
R7630:Fryl
|
UTSW |
5 |
73,267,588 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7774:Fryl
|
UTSW |
5 |
73,240,727 (GRCm39) |
missense |
probably benign |
0.12 |
R7777:Fryl
|
UTSW |
5 |
73,228,641 (GRCm39) |
missense |
probably damaging |
0.98 |
R7917:Fryl
|
UTSW |
5 |
73,211,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R7920:Fryl
|
UTSW |
5 |
73,259,150 (GRCm39) |
splice site |
probably null |
|
R8110:Fryl
|
UTSW |
5 |
73,290,620 (GRCm39) |
missense |
probably benign |
0.10 |
R8120:Fryl
|
UTSW |
5 |
73,228,527 (GRCm39) |
missense |
probably benign |
0.01 |
R8143:Fryl
|
UTSW |
5 |
73,207,682 (GRCm39) |
missense |
probably benign |
0.00 |
R8207:Fryl
|
UTSW |
5 |
73,257,843 (GRCm39) |
splice site |
probably null |
|
R8263:Fryl
|
UTSW |
5 |
73,238,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R8350:Fryl
|
UTSW |
5 |
73,226,073 (GRCm39) |
missense |
probably benign |
|
R8359:Fryl
|
UTSW |
5 |
73,233,276 (GRCm39) |
missense |
probably benign |
0.39 |
R8387:Fryl
|
UTSW |
5 |
73,293,663 (GRCm39) |
critical splice donor site |
probably null |
|
R8403:Fryl
|
UTSW |
5 |
73,275,790 (GRCm39) |
makesense |
probably null |
|
R8450:Fryl
|
UTSW |
5 |
73,226,073 (GRCm39) |
missense |
probably benign |
|
R8514:Fryl
|
UTSW |
5 |
73,242,699 (GRCm39) |
missense |
probably benign |
|
R8536:Fryl
|
UTSW |
5 |
73,257,696 (GRCm39) |
missense |
probably damaging |
0.99 |
R8703:Fryl
|
UTSW |
5 |
73,247,997 (GRCm39) |
missense |
probably damaging |
0.99 |
R8708:Fryl
|
UTSW |
5 |
73,289,905 (GRCm39) |
missense |
probably benign |
0.01 |
R8783:Fryl
|
UTSW |
5 |
73,226,185 (GRCm39) |
missense |
probably benign |
0.45 |
R9028:Fryl
|
UTSW |
5 |
73,255,609 (GRCm39) |
missense |
probably benign |
0.18 |
R9045:Fryl
|
UTSW |
5 |
73,182,118 (GRCm39) |
missense |
|
|
R9063:Fryl
|
UTSW |
5 |
73,238,346 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9096:Fryl
|
UTSW |
5 |
73,265,920 (GRCm39) |
missense |
probably benign |
0.01 |
R9244:Fryl
|
UTSW |
5 |
73,348,862 (GRCm39) |
intron |
probably benign |
|
R9345:Fryl
|
UTSW |
5 |
73,207,754 (GRCm39) |
missense |
probably benign |
|
R9381:Fryl
|
UTSW |
5 |
73,240,637 (GRCm39) |
missense |
probably benign |
0.24 |
R9386:Fryl
|
UTSW |
5 |
73,349,152 (GRCm39) |
missense |
unknown |
|
R9401:Fryl
|
UTSW |
5 |
73,222,563 (GRCm39) |
nonsense |
probably null |
|
R9497:Fryl
|
UTSW |
5 |
73,215,134 (GRCm39) |
missense |
|
|
R9514:Fryl
|
UTSW |
5 |
73,262,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R9570:Fryl
|
UTSW |
5 |
73,179,498 (GRCm39) |
missense |
probably benign |
0.02 |
R9654:Fryl
|
UTSW |
5 |
73,275,801 (GRCm39) |
missense |
probably benign |
|
R9665:Fryl
|
UTSW |
5 |
73,222,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R9685:Fryl
|
UTSW |
5 |
73,216,879 (GRCm39) |
missense |
probably damaging |
0.99 |
R9798:Fryl
|
UTSW |
5 |
73,192,402 (GRCm39) |
missense |
probably benign |
|
Z1088:Fryl
|
UTSW |
5 |
73,248,081 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Fryl
|
UTSW |
5 |
73,248,052 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Fryl
|
UTSW |
5 |
73,230,180 (GRCm39) |
missense |
probably benign |
|
Z1177:Fryl
|
UTSW |
5 |
73,198,938 (GRCm39) |
critical splice acceptor site |
probably null |
|
|