Other mutations in this stock |
Total: 130 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123L14Rik |
A |
G |
6: 96,165,269 (GRCm38) |
S265P |
possibly damaging |
Het |
Abcc1 |
T |
C |
16: 14,396,393 (GRCm38) |
Y191H |
probably damaging |
Het |
Aco1 |
T |
C |
4: 40,167,193 (GRCm38) |
|
probably null |
Het |
Adap1 |
A |
G |
5: 139,273,341 (GRCm38) |
Y364H |
probably benign |
Het |
Add2 |
T |
C |
6: 86,096,756 (GRCm38) |
F209S |
probably damaging |
Het |
Adgb |
A |
T |
10: 10,395,249 (GRCm38) |
D883E |
probably benign |
Het |
Als2cr12 |
A |
T |
1: 58,659,278 (GRCm38) |
V327D |
possibly damaging |
Het |
Anapc1 |
C |
A |
2: 128,633,415 (GRCm38) |
R1381S |
probably benign |
Het |
Aoah |
A |
G |
13: 20,794,394 (GRCm38) |
M1V |
probably null |
Het |
Arap1 |
C |
A |
7: 101,373,015 (GRCm38) |
A8E |
probably damaging |
Het |
Arhgap10 |
A |
G |
8: 77,409,626 (GRCm38) |
F319S |
possibly damaging |
Het |
Btrc |
T |
G |
19: 45,527,343 (GRCm38) |
I480S |
probably damaging |
Het |
Cabin1 |
A |
T |
10: 75,735,090 (GRCm38) |
V784E |
possibly damaging |
Het |
Card9 |
T |
A |
2: 26,354,873 (GRCm38) |
|
probably null |
Het |
Cdk18 |
A |
G |
1: 132,117,821 (GRCm38) |
I238T |
possibly damaging |
Het |
Clec12a |
A |
C |
6: 129,350,481 (GRCm38) |
T21P |
possibly damaging |
Het |
Commd3 |
A |
T |
2: 18,673,963 (GRCm38) |
I70F |
probably benign |
Het |
Cspg5 |
G |
A |
9: 110,251,026 (GRCm38) |
V340M |
probably damaging |
Het |
Cyb5r4 |
G |
A |
9: 87,055,849 (GRCm38) |
S307N |
possibly damaging |
Het |
Cyp26c1 |
T |
A |
19: 37,687,377 (GRCm38) |
F230I |
probably damaging |
Het |
Ddx11 |
A |
G |
17: 66,130,728 (GRCm38) |
M150V |
probably benign |
Het |
Dennd4b |
A |
G |
3: 90,268,773 (GRCm38) |
Y190C |
probably damaging |
Het |
Det1 |
A |
G |
7: 78,843,443 (GRCm38) |
V271A |
probably benign |
Het |
Dgkd |
C |
A |
1: 87,929,827 (GRCm38) |
P754T |
possibly damaging |
Het |
Dhx36 |
T |
C |
3: 62,479,385 (GRCm38) |
S649G |
probably benign |
Het |
Dlgap5 |
A |
G |
14: 47,416,386 (GRCm38) |
I62T |
possibly damaging |
Het |
Dmgdh |
A |
G |
13: 93,720,559 (GRCm38) |
M724V |
probably benign |
Het |
Dnah7a |
A |
G |
1: 53,684,983 (GRCm38) |
S108P |
probably benign |
Het |
Dock4 |
A |
T |
12: 40,710,798 (GRCm38) |
K495M |
probably damaging |
Het |
Dse |
A |
G |
10: 34,160,206 (GRCm38) |
Y225H |
probably damaging |
Het |
Emx1 |
G |
A |
6: 85,203,934 (GRCm38) |
R211K |
probably damaging |
Het |
Ergic2 |
A |
G |
6: 148,199,354 (GRCm38) |
|
probably null |
Het |
Fbxo27 |
G |
A |
7: 28,698,372 (GRCm38) |
C277Y |
possibly damaging |
Het |
Fcrl1 |
T |
C |
3: 87,376,520 (GRCm38) |
I9T |
possibly damaging |
Het |
Fjx1 |
T |
C |
2: 102,450,807 (GRCm38) |
E261G |
probably benign |
Het |
Flnb |
C |
T |
14: 7,884,735 (GRCm38) |
Q445* |
probably null |
Het |
Flrt2 |
G |
A |
12: 95,780,300 (GRCm38) |
V471I |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,991,550 (GRCm38) |
K5876E |
probably benign |
Het |
Galnt10 |
T |
C |
11: 57,765,617 (GRCm38) |
L209P |
probably damaging |
Het |
Gata5 |
A |
T |
2: 180,326,936 (GRCm38) |
S382T |
possibly damaging |
Het |
Glt6d1 |
C |
A |
2: 25,794,413 (GRCm38) |
V194L |
probably damaging |
Het |
Gm10803 |
T |
G |
2: 93,563,943 (GRCm38) |
V20G |
unknown |
Het |
Gm44511 |
T |
G |
6: 128,820,271 (GRCm38) |
T52P |
probably damaging |
Het |
Gpat4 |
A |
T |
8: 23,182,936 (GRCm38) |
L88Q |
possibly damaging |
Het |
Gpr15 |
T |
A |
16: 58,718,007 (GRCm38) |
I240L |
probably benign |
Het |
Hivep2 |
A |
T |
10: 14,132,709 (GRCm38) |
I1684F |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,649,676 (GRCm38) |
T3366A |
probably benign |
Het |
Hnmt |
A |
G |
2: 24,003,882 (GRCm38) |
V200A |
possibly damaging |
Het |
Hps6 |
A |
T |
19: 46,004,335 (GRCm38) |
H237L |
probably benign |
Het |
Hspg2 |
C |
T |
4: 137,564,895 (GRCm38) |
P4033S |
probably damaging |
Het |
Irf9 |
T |
A |
14: 55,607,717 (GRCm38) |
S297T |
possibly damaging |
Het |
Kdm3b |
T |
C |
18: 34,812,395 (GRCm38) |
V753A |
possibly damaging |
Het |
Kif21a |
G |
A |
15: 90,970,848 (GRCm38) |
A703V |
probably damaging |
Het |
Kif27 |
T |
G |
13: 58,293,123 (GRCm38) |
R1159S |
probably benign |
Het |
Krtap4-16 |
A |
G |
11: 99,851,547 (GRCm38) |
V9A |
unknown |
Het |
Lama2 |
G |
T |
10: 27,422,618 (GRCm38) |
P161T |
probably damaging |
Het |
Ltbp4 |
G |
A |
7: 27,329,018 (GRCm38) |
P273L |
unknown |
Het |
Lvrn |
T |
A |
18: 46,894,717 (GRCm38) |
S866R |
probably damaging |
Het |
Med13 |
A |
G |
11: 86,298,979 (GRCm38) |
Y1035H |
probably damaging |
Het |
Mertk |
T |
A |
2: 128,759,090 (GRCm38) |
N331K |
probably damaging |
Het |
Mios |
T |
A |
6: 8,215,437 (GRCm38) |
F211Y |
probably benign |
Het |
Mpeg1 |
G |
A |
19: 12,462,911 (GRCm38) |
V578M |
probably damaging |
Het |
Mphosph9 |
A |
T |
5: 124,315,701 (GRCm38) |
S183T |
possibly damaging |
Het |
Mrto4 |
A |
T |
4: 139,349,638 (GRCm38) |
I56N |
probably damaging |
Het |
Muc5b |
T |
C |
7: 141,862,637 (GRCm38) |
C3107R |
possibly damaging |
Het |
Ncoa2 |
A |
G |
1: 13,160,252 (GRCm38) |
Y1023H |
probably damaging |
Het |
Nlrp2 |
T |
C |
7: 5,327,738 (GRCm38) |
E553G |
probably damaging |
Het |
Nlrp6 |
GAGAAGAAGAAGAAGAAGAAGA |
GAGAAGAAGAAGAAGAAGA |
7: 140,924,113 (GRCm38) |
|
probably benign |
Het |
Nr2f1 |
T |
C |
13: 78,189,816 (GRCm38) |
T237A |
probably damaging |
Het |
Nup205 |
C |
A |
6: 35,233,366 (GRCm38) |
Q1621K |
probably benign |
Het |
Nxpe2 |
T |
A |
9: 48,319,726 (GRCm38) |
S448C |
probably benign |
Het |
Ogdh |
T |
A |
11: 6,346,638 (GRCm38) |
C498S |
possibly damaging |
Het |
Olfr1176 |
T |
C |
2: 88,340,201 (GRCm38) |
L212P |
probably damaging |
Het |
Olfr281 |
T |
C |
15: 98,456,753 (GRCm38) |
S148P |
probably damaging |
Het |
Olfr294 |
A |
T |
7: 86,616,431 (GRCm38) |
F71L |
probably benign |
Het |
Olfr414 |
A |
T |
1: 174,430,905 (GRCm38) |
K159M |
probably damaging |
Het |
Olfr697 |
T |
C |
7: 106,741,394 (GRCm38) |
E180G |
probably damaging |
Het |
Olfr715 |
A |
T |
7: 107,128,510 (GRCm38) |
D294E |
possibly damaging |
Het |
Olfr994 |
T |
C |
2: 85,430,619 (GRCm38) |
D70G |
probably damaging |
Het |
Oplah |
G |
A |
15: 76,297,464 (GRCm38) |
T1119I |
probably damaging |
Het |
Pcdhb9 |
T |
A |
18: 37,403,316 (GRCm38) |
Y788N |
probably damaging |
Het |
Pcsk5 |
T |
C |
19: 17,433,418 (GRCm38) |
D1870G |
unknown |
Het |
Pde6g |
A |
G |
11: 120,448,136 (GRCm38) |
L76P |
probably damaging |
Het |
Peak1 |
A |
T |
9: 56,206,789 (GRCm38) |
Y593N |
probably damaging |
Het |
Pfas |
C |
T |
11: 68,994,284 (GRCm38) |
G16R |
probably damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,043,231 (GRCm38) |
|
probably null |
Het |
Pla2g3 |
C |
T |
11: 3,490,983 (GRCm38) |
T316I |
probably benign |
Het |
Ptpru |
T |
A |
4: 131,803,477 (GRCm38) |
I489F |
probably damaging |
Het |
Rere |
T |
G |
4: 150,468,790 (GRCm38) |
H146Q |
probably benign |
Het |
Rundc1 |
A |
T |
11: 101,431,496 (GRCm38) |
Q272L |
probably damaging |
Het |
Scml4 |
T |
C |
10: 42,956,021 (GRCm38) |
L305P |
probably damaging |
Het |
Sec16a |
A |
T |
2: 26,430,132 (GRCm38) |
H1431Q |
probably benign |
Het |
Serpina1a |
G |
A |
12: 103,853,800 (GRCm38) |
Q373* |
probably null |
Het |
Shank1 |
A |
T |
7: 44,325,377 (GRCm38) |
N377I |
unknown |
Het |
Shc2 |
T |
C |
10: 79,626,791 (GRCm38) |
|
probably null |
Het |
Slc22a29 |
C |
A |
19: 8,169,193 (GRCm38) |
R415M |
probably benign |
Het |
Slc7a2 |
A |
T |
8: 40,914,965 (GRCm38) |
I589F |
probably damaging |
Het |
Smim8 |
C |
T |
4: 34,771,316 (GRCm38) |
R26Q |
probably damaging |
Het |
Smox |
C |
A |
2: 131,520,464 (GRCm38) |
A221D |
probably damaging |
Het |
Sox5 |
A |
G |
6: 143,874,105 (GRCm38) |
S62P |
possibly damaging |
Het |
Spg21 |
A |
C |
9: 65,484,492 (GRCm38) |
K240N |
probably damaging |
Het |
Sv2c |
C |
T |
13: 95,976,645 (GRCm38) |
V599M |
probably damaging |
Het |
Tanc2 |
T |
A |
11: 105,910,295 (GRCm38) |
H1112Q |
probably damaging |
Het |
Tbata |
T |
C |
10: 61,175,844 (GRCm38) |
I58T |
possibly damaging |
Het |
Tbc1d2 |
T |
G |
4: 46,606,419 (GRCm38) |
Y842S |
probably benign |
Het |
Tctn1 |
A |
T |
5: 122,241,840 (GRCm38) |
|
probably null |
Het |
Tenm1 |
T |
C |
X: 42,827,201 (GRCm38) |
D402G |
probably benign |
Het |
Tfcp2l1 |
T |
C |
1: 118,669,389 (GRCm38) |
V400A |
probably benign |
Het |
Tm9sf2 |
T |
A |
14: 122,126,164 (GRCm38) |
L99I |
probably benign |
Het |
Top2a |
T |
C |
11: 98,995,977 (GRCm38) |
|
probably null |
Het |
Traf7 |
C |
A |
17: 24,513,281 (GRCm38) |
G191C |
probably damaging |
Het |
Trpm1 |
T |
A |
7: 64,230,230 (GRCm38) |
L661Q |
probably damaging |
Het |
Ttc30b |
C |
T |
2: 75,937,099 (GRCm38) |
E437K |
probably benign |
Het |
Ttn |
T |
C |
2: 76,750,623 (GRCm38) |
I23309V |
probably benign |
Het |
Usp50 |
T |
C |
2: 126,777,961 (GRCm38) |
K199E |
possibly damaging |
Het |
Vmn1r218 |
T |
C |
13: 23,136,513 (GRCm38) |
F10S |
probably damaging |
Het |
Vmn2r89 |
C |
A |
14: 51,457,440 (GRCm38) |
T459K |
probably benign |
Het |
Vps13a |
T |
G |
19: 16,677,938 (GRCm38) |
S1909R |
possibly damaging |
Het |
Vwa5b2 |
T |
C |
16: 20,602,191 (GRCm38) |
|
probably null |
Het |
Vwa8 |
A |
G |
14: 78,982,360 (GRCm38) |
H516R |
possibly damaging |
Het |
Wnk1 |
T |
C |
6: 119,969,247 (GRCm38) |
I648M |
probably damaging |
Het |
Zfat |
G |
C |
15: 68,146,543 (GRCm38) |
P974R |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,423,253 (GRCm38) |
I1601K |
probably benign |
Het |
Zfp239 |
A |
G |
6: 117,871,817 (GRCm38) |
K172R |
probably benign |
Het |
Zfp335 |
C |
T |
2: 164,894,802 (GRCm38) |
G971D |
probably damaging |
Het |
Zfp532 |
A |
T |
18: 65,624,492 (GRCm38) |
I499F |
probably damaging |
Het |
Zfp647 |
T |
C |
15: 76,911,114 (GRCm38) |
T449A |
possibly damaging |
Het |
Zfp938 |
C |
T |
10: 82,225,631 (GRCm38) |
G385D |
probably damaging |
Het |
Zfp959 |
T |
G |
17: 55,897,404 (GRCm38) |
V147G |
probably damaging |
Het |
Znfx1 |
A |
T |
2: 167,050,350 (GRCm38) |
C649S |
probably damaging |
Het |
|
Other mutations in Frmd4a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00339:Frmd4a
|
APN |
2 |
4,594,714 (GRCm38) |
missense |
probably benign |
0.00 |
IGL00508:Frmd4a
|
APN |
2 |
4,594,734 (GRCm38) |
nonsense |
probably null |
|
IGL01331:Frmd4a
|
APN |
2 |
4,602,225 (GRCm38) |
missense |
probably benign |
0.32 |
IGL01774:Frmd4a
|
APN |
2 |
4,535,236 (GRCm38) |
splice site |
probably benign |
|
IGL01909:Frmd4a
|
APN |
2 |
4,604,033 (GRCm38) |
missense |
probably benign |
0.11 |
IGL02170:Frmd4a
|
APN |
2 |
4,566,177 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL02269:Frmd4a
|
APN |
2 |
4,604,234 (GRCm38) |
missense |
probably benign |
0.19 |
IGL02377:Frmd4a
|
APN |
2 |
4,534,574 (GRCm38) |
missense |
possibly damaging |
0.47 |
IGL03308:Frmd4a
|
APN |
2 |
4,498,026 (GRCm38) |
missense |
possibly damaging |
0.95 |
R0066:Frmd4a
|
UTSW |
2 |
4,473,152 (GRCm38) |
missense |
probably damaging |
1.00 |
R0066:Frmd4a
|
UTSW |
2 |
4,473,152 (GRCm38) |
missense |
probably damaging |
1.00 |
R0081:Frmd4a
|
UTSW |
2 |
4,572,441 (GRCm38) |
critical splice donor site |
probably null |
|
R0128:Frmd4a
|
UTSW |
2 |
4,604,092 (GRCm38) |
missense |
probably damaging |
0.98 |
R0130:Frmd4a
|
UTSW |
2 |
4,604,092 (GRCm38) |
missense |
probably damaging |
0.98 |
R0376:Frmd4a
|
UTSW |
2 |
4,572,387 (GRCm38) |
missense |
probably damaging |
0.97 |
R0529:Frmd4a
|
UTSW |
2 |
4,606,023 (GRCm38) |
missense |
probably damaging |
1.00 |
R0549:Frmd4a
|
UTSW |
2 |
4,603,967 (GRCm38) |
missense |
possibly damaging |
0.76 |
R1593:Frmd4a
|
UTSW |
2 |
4,473,188 (GRCm38) |
missense |
probably damaging |
1.00 |
R2002:Frmd4a
|
UTSW |
2 |
4,572,365 (GRCm38) |
missense |
probably damaging |
1.00 |
R2100:Frmd4a
|
UTSW |
2 |
4,606,023 (GRCm38) |
missense |
probably damaging |
1.00 |
R2310:Frmd4a
|
UTSW |
2 |
4,572,399 (GRCm38) |
frame shift |
probably null |
|
R2340:Frmd4a
|
UTSW |
2 |
4,586,376 (GRCm38) |
missense |
probably damaging |
1.00 |
R2426:Frmd4a
|
UTSW |
2 |
4,529,862 (GRCm38) |
missense |
probably damaging |
1.00 |
R2680:Frmd4a
|
UTSW |
2 |
4,534,553 (GRCm38) |
missense |
probably damaging |
1.00 |
R3409:Frmd4a
|
UTSW |
2 |
4,153,028 (GRCm38) |
intron |
probably benign |
|
R3772:Frmd4a
|
UTSW |
2 |
4,590,622 (GRCm38) |
missense |
probably damaging |
0.99 |
R3773:Frmd4a
|
UTSW |
2 |
4,590,622 (GRCm38) |
missense |
probably damaging |
0.99 |
R3932:Frmd4a
|
UTSW |
2 |
4,537,260 (GRCm38) |
missense |
probably damaging |
1.00 |
R4094:Frmd4a
|
UTSW |
2 |
4,611,032 (GRCm38) |
missense |
probably damaging |
1.00 |
R4226:Frmd4a
|
UTSW |
2 |
4,333,078 (GRCm38) |
missense |
probably benign |
0.00 |
R4299:Frmd4a
|
UTSW |
2 |
4,333,071 (GRCm38) |
missense |
probably benign |
0.02 |
R4304:Frmd4a
|
UTSW |
2 |
4,333,078 (GRCm38) |
missense |
probably benign |
0.00 |
R4306:Frmd4a
|
UTSW |
2 |
4,333,078 (GRCm38) |
missense |
probably benign |
0.00 |
R4307:Frmd4a
|
UTSW |
2 |
4,333,078 (GRCm38) |
missense |
probably benign |
0.00 |
R4346:Frmd4a
|
UTSW |
2 |
4,608,033 (GRCm38) |
missense |
possibly damaging |
0.92 |
R4360:Frmd4a
|
UTSW |
2 |
4,601,241 (GRCm38) |
missense |
probably damaging |
1.00 |
R4384:Frmd4a
|
UTSW |
2 |
4,594,563 (GRCm38) |
nonsense |
probably null |
|
R4547:Frmd4a
|
UTSW |
2 |
4,473,145 (GRCm38) |
missense |
probably damaging |
1.00 |
R4575:Frmd4a
|
UTSW |
2 |
4,603,679 (GRCm38) |
missense |
possibly damaging |
0.83 |
R4577:Frmd4a
|
UTSW |
2 |
4,603,679 (GRCm38) |
missense |
possibly damaging |
0.83 |
R4578:Frmd4a
|
UTSW |
2 |
4,603,679 (GRCm38) |
missense |
possibly damaging |
0.83 |
R4688:Frmd4a
|
UTSW |
2 |
4,537,311 (GRCm38) |
missense |
possibly damaging |
0.81 |
R4764:Frmd4a
|
UTSW |
2 |
4,603,448 (GRCm38) |
missense |
probably damaging |
1.00 |
R4826:Frmd4a
|
UTSW |
2 |
4,601,297 (GRCm38) |
missense |
probably damaging |
1.00 |
R4879:Frmd4a
|
UTSW |
2 |
4,529,817 (GRCm38) |
missense |
probably damaging |
1.00 |
R5053:Frmd4a
|
UTSW |
2 |
4,603,921 (GRCm38) |
missense |
probably damaging |
1.00 |
R5392:Frmd4a
|
UTSW |
2 |
4,594,573 (GRCm38) |
missense |
probably damaging |
1.00 |
R5733:Frmd4a
|
UTSW |
2 |
4,300,957 (GRCm38) |
missense |
possibly damaging |
0.53 |
R5762:Frmd4a
|
UTSW |
2 |
4,484,065 (GRCm38) |
missense |
probably damaging |
1.00 |
R5920:Frmd4a
|
UTSW |
2 |
4,333,116 (GRCm38) |
missense |
probably benign |
0.02 |
R5932:Frmd4a
|
UTSW |
2 |
4,529,839 (GRCm38) |
missense |
probably damaging |
1.00 |
R6117:Frmd4a
|
UTSW |
2 |
4,602,249 (GRCm38) |
missense |
possibly damaging |
0.66 |
R6328:Frmd4a
|
UTSW |
2 |
4,590,698 (GRCm38) |
missense |
probably damaging |
0.99 |
R6622:Frmd4a
|
UTSW |
2 |
4,606,062 (GRCm38) |
missense |
probably benign |
0.00 |
R6903:Frmd4a
|
UTSW |
2 |
4,586,456 (GRCm38) |
missense |
probably damaging |
1.00 |
R7065:Frmd4a
|
UTSW |
2 |
4,566,112 (GRCm38) |
|
|
|
R7098:Frmd4a
|
UTSW |
2 |
4,572,433 (GRCm38) |
missense |
probably damaging |
1.00 |
R7258:Frmd4a
|
UTSW |
2 |
4,300,953 (GRCm38) |
missense |
probably benign |
|
R7336:Frmd4a
|
UTSW |
2 |
4,473,214 (GRCm38) |
missense |
possibly damaging |
0.92 |
R7582:Frmd4a
|
UTSW |
2 |
4,594,597 (GRCm38) |
frame shift |
probably null |
|
R7607:Frmd4a
|
UTSW |
2 |
4,591,936 (GRCm38) |
nonsense |
probably null |
|
R7697:Frmd4a
|
UTSW |
2 |
4,484,081 (GRCm38) |
missense |
probably damaging |
1.00 |
R7750:Frmd4a
|
UTSW |
2 |
4,601,349 (GRCm38) |
missense |
probably benign |
0.14 |
R7795:Frmd4a
|
UTSW |
2 |
4,590,695 (GRCm38) |
missense |
probably damaging |
1.00 |
R7848:Frmd4a
|
UTSW |
2 |
4,591,917 (GRCm38) |
intron |
probably benign |
|
R7899:Frmd4a
|
UTSW |
2 |
4,604,089 (GRCm38) |
missense |
probably damaging |
1.00 |
R8024:Frmd4a
|
UTSW |
2 |
4,603,702 (GRCm38) |
missense |
probably damaging |
1.00 |
R8399:Frmd4a
|
UTSW |
2 |
4,572,433 (GRCm38) |
missense |
probably damaging |
1.00 |
R8778:Frmd4a
|
UTSW |
2 |
4,473,215 (GRCm38) |
missense |
probably damaging |
1.00 |
R8876:Frmd4a
|
UTSW |
2 |
4,601,300 (GRCm38) |
missense |
probably damaging |
0.99 |
R9074:Frmd4a
|
UTSW |
2 |
4,603,954 (GRCm38) |
missense |
probably damaging |
1.00 |
R9075:Frmd4a
|
UTSW |
2 |
4,603,954 (GRCm38) |
missense |
probably damaging |
1.00 |
R9076:Frmd4a
|
UTSW |
2 |
4,603,954 (GRCm38) |
missense |
probably damaging |
1.00 |
R9105:Frmd4a
|
UTSW |
2 |
4,535,183 (GRCm38) |
missense |
probably damaging |
0.96 |
R9213:Frmd4a
|
UTSW |
2 |
4,603,561 (GRCm38) |
missense |
probably damaging |
1.00 |
R9227:Frmd4a
|
UTSW |
2 |
4,608,033 (GRCm38) |
missense |
possibly damaging |
0.92 |
R9230:Frmd4a
|
UTSW |
2 |
4,608,033 (GRCm38) |
missense |
possibly damaging |
0.92 |
R9235:Frmd4a
|
UTSW |
2 |
4,594,555 (GRCm38) |
missense |
probably damaging |
0.99 |
R9266:Frmd4a
|
UTSW |
2 |
4,606,035 (GRCm38) |
missense |
probably damaging |
0.99 |
R9301:Frmd4a
|
UTSW |
2 |
4,153,093 (GRCm38) |
missense |
probably benign |
0.27 |
R9307:Frmd4a
|
UTSW |
2 |
4,604,233 (GRCm38) |
missense |
probably benign |
|
R9365:Frmd4a
|
UTSW |
2 |
4,602,162 (GRCm38) |
missense |
probably benign |
0.01 |
R9476:Frmd4a
|
UTSW |
2 |
4,603,513 (GRCm38) |
missense |
probably benign |
0.32 |
R9484:Frmd4a
|
UTSW |
2 |
4,604,215 (GRCm38) |
missense |
possibly damaging |
0.49 |
R9510:Frmd4a
|
UTSW |
2 |
4,603,513 (GRCm38) |
missense |
probably benign |
0.32 |
R9513:Frmd4a
|
UTSW |
2 |
4,603,900 (GRCm38) |
missense |
probably damaging |
0.99 |
Z1176:Frmd4a
|
UTSW |
2 |
4,498,021 (GRCm38) |
missense |
probably damaging |
1.00 |
|