Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
A |
T |
9: 53,336,830 (GRCm39) |
M45L |
probably benign |
Het |
Acss2 |
T |
C |
2: 155,403,063 (GRCm39) |
F627L |
probably damaging |
Het |
Akap8 |
A |
G |
17: 32,535,184 (GRCm39) |
S277P |
probably damaging |
Het |
Akap9 |
T |
A |
5: 4,051,418 (GRCm39) |
M1395K |
probably damaging |
Het |
Ank1 |
A |
G |
8: 23,612,893 (GRCm39) |
D1468G |
probably benign |
Het |
Apoe |
A |
G |
7: 19,430,846 (GRCm39) |
V121A |
probably benign |
Het |
Aqp9 |
A |
T |
9: 71,070,331 (GRCm39) |
L12H |
probably damaging |
Het |
Atp2b4 |
G |
A |
1: 133,639,529 (GRCm39) |
A1115V |
probably benign |
Het |
Atp2b4 |
G |
A |
1: 133,667,134 (GRCm39) |
P139L |
probably benign |
Het |
B430218F22Rik |
T |
C |
13: 118,523,980 (GRCm39) |
|
probably benign |
Het |
Bltp2 |
T |
A |
11: 78,154,854 (GRCm39) |
L122H |
probably damaging |
Het |
Brsk1 |
A |
G |
7: 4,711,866 (GRCm39) |
E572G |
possibly damaging |
Het |
C6 |
T |
C |
15: 4,811,394 (GRCm39) |
I414T |
probably benign |
Het |
C8b |
T |
A |
4: 104,644,083 (GRCm39) |
M250K |
probably benign |
Het |
Camk1g |
T |
A |
1: 193,044,393 (GRCm39) |
E7V |
probably benign |
Het |
Clcc1 |
A |
G |
3: 108,580,236 (GRCm39) |
|
probably null |
Het |
Col4a3 |
G |
T |
1: 82,694,018 (GRCm39) |
|
probably null |
Het |
Cox5b |
T |
A |
1: 36,732,310 (GRCm39) |
W104R |
probably damaging |
Het |
Cyp2c55 |
A |
C |
19: 39,019,815 (GRCm39) |
H251P |
probably damaging |
Het |
Cyp2c67 |
G |
A |
19: 39,632,188 (GRCm39) |
T60I |
probably benign |
Het |
Defb42 |
T |
A |
14: 63,285,824 (GRCm39) |
V68E |
probably benign |
Het |
Ercc4 |
T |
A |
16: 12,941,287 (GRCm39) |
I225N |
probably damaging |
Het |
Fam120b |
G |
T |
17: 15,622,658 (GRCm39) |
C212F |
probably damaging |
Het |
Fgf10 |
T |
C |
13: 118,918,045 (GRCm39) |
V111A |
probably benign |
Het |
Fras1 |
T |
C |
5: 96,929,518 (GRCm39) |
V3974A |
probably benign |
Het |
Galnt4 |
T |
C |
10: 98,944,362 (GRCm39) |
V29A |
probably benign |
Het |
Gpr26 |
T |
C |
7: 131,569,230 (GRCm39) |
Y192H |
probably damaging |
Het |
Heatr9 |
A |
T |
11: 83,407,475 (GRCm39) |
L236Q |
probably damaging |
Het |
Hivep3 |
C |
A |
4: 119,955,020 (GRCm39) |
P1112H |
probably damaging |
Het |
Hnf4g |
A |
G |
3: 3,708,069 (GRCm39) |
Y106C |
possibly damaging |
Het |
Hnrnpdl |
A |
T |
5: 100,185,783 (GRCm39) |
Y69* |
probably null |
Het |
Itgb1 |
G |
A |
8: 129,443,703 (GRCm39) |
A320T |
probably damaging |
Het |
Kcna2 |
T |
C |
3: 107,012,733 (GRCm39) |
I438T |
probably benign |
Het |
Kif24 |
A |
G |
4: 41,397,545 (GRCm39) |
|
probably null |
Het |
Klhl1 |
G |
A |
14: 96,389,402 (GRCm39) |
T584I |
probably benign |
Het |
Ltbp1 |
A |
G |
17: 75,532,199 (GRCm39) |
D91G |
probably damaging |
Het |
Mdga2 |
T |
C |
12: 66,844,427 (GRCm39) |
I190M |
probably damaging |
Het |
Meis2 |
G |
A |
2: 115,830,686 (GRCm39) |
R276C |
probably damaging |
Het |
Mob4 |
C |
T |
1: 55,191,855 (GRCm39) |
R190W |
probably damaging |
Het |
Mrgpra2a |
A |
G |
7: 47,077,114 (GRCm39) |
I48T |
possibly damaging |
Het |
Mst1 |
T |
C |
9: 107,960,826 (GRCm39) |
V481A |
probably benign |
Het |
Mttp |
A |
T |
3: 137,821,832 (GRCm39) |
V245E |
possibly damaging |
Het |
Nbn |
T |
A |
4: 15,981,470 (GRCm39) |
S521T |
probably benign |
Het |
Neb |
G |
T |
2: 52,083,243 (GRCm39) |
T5654N |
probably damaging |
Het |
Nlrp9a |
A |
T |
7: 26,256,866 (GRCm39) |
K161N |
probably damaging |
Het |
Nod2 |
T |
G |
8: 89,390,902 (GRCm39) |
F388C |
possibly damaging |
Het |
Or3a1 |
G |
T |
11: 74,225,402 (GRCm39) |
F218L |
probably benign |
Het |
Or4a75 |
G |
T |
2: 89,447,814 (GRCm39) |
H241N |
possibly damaging |
Het |
Or4f58 |
A |
G |
2: 111,851,332 (GRCm39) |
F289S |
possibly damaging |
Het |
Or52e2 |
A |
T |
7: 102,804,332 (GRCm39) |
N207K |
probably benign |
Het |
Or7a38 |
T |
A |
10: 78,753,361 (GRCm39) |
I229N |
probably damaging |
Het |
Or7g25 |
G |
A |
9: 19,160,153 (GRCm39) |
L181F |
possibly damaging |
Het |
P2ry1 |
A |
G |
3: 60,911,898 (GRCm39) |
S346G |
probably benign |
Het |
Polr1f |
T |
A |
12: 33,487,679 (GRCm39) |
|
probably null |
Het |
Prkcd |
A |
G |
14: 30,321,623 (GRCm39) |
F524L |
probably benign |
Het |
Qrfprl |
T |
C |
6: 65,429,898 (GRCm39) |
I198T |
probably benign |
Het |
Ramp3 |
A |
T |
11: 6,624,843 (GRCm39) |
M46L |
probably benign |
Het |
Rint1 |
T |
C |
5: 24,014,791 (GRCm39) |
Y278H |
probably damaging |
Het |
Skint11 |
C |
T |
4: 114,051,874 (GRCm39) |
T74I |
probably benign |
Het |
Slc10a7 |
T |
C |
8: 79,433,579 (GRCm39) |
|
probably null |
Het |
Slc45a2 |
T |
A |
15: 11,028,016 (GRCm39) |
Y528* |
probably null |
Het |
Slit1 |
A |
G |
19: 41,637,452 (GRCm39) |
F329L |
probably damaging |
Het |
Sltm |
A |
T |
9: 70,498,892 (GRCm39) |
M989L |
possibly damaging |
Het |
Smad9 |
A |
T |
3: 54,701,874 (GRCm39) |
T372S |
possibly damaging |
Het |
Snrpc |
T |
A |
17: 28,061,306 (GRCm39) |
Y38* |
probably null |
Het |
Spag17 |
A |
G |
3: 100,010,701 (GRCm39) |
K2065R |
possibly damaging |
Het |
Stxbp4 |
T |
A |
11: 90,498,197 (GRCm39) |
K87N |
probably damaging |
Het |
Tbc1d23 |
AT |
ATT |
16: 57,019,258 (GRCm39) |
|
probably null |
Het |
Tgfb1i1 |
A |
T |
7: 127,848,571 (GRCm39) |
M96L |
probably damaging |
Het |
Tnc |
T |
A |
4: 63,885,580 (GRCm39) |
I1841F |
probably damaging |
Het |
Ubap2 |
G |
T |
4: 41,211,771 (GRCm39) |
H63Q |
probably damaging |
Het |
Vps13a |
T |
C |
19: 16,632,580 (GRCm39) |
N2592S |
probably benign |
Het |
Xdh |
G |
A |
17: 74,193,381 (GRCm39) |
P1305L |
probably benign |
Het |
Xrn1 |
G |
A |
9: 95,921,862 (GRCm39) |
R1425K |
probably benign |
Het |
Zfp418 |
G |
A |
7: 7,185,762 (GRCm39) |
R575Q |
possibly damaging |
Het |
Zfp608 |
T |
A |
18: 55,027,544 (GRCm39) |
Q1424H |
probably damaging |
Het |
Zfp839 |
C |
A |
12: 110,821,635 (GRCm39) |
L150I |
possibly damaging |
Het |
|
Other mutations in Fn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00236:Fn1
|
APN |
1 |
71,692,032 (GRCm39) |
missense |
probably benign |
0.28 |
IGL00402:Fn1
|
APN |
1 |
71,680,322 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00946:Fn1
|
APN |
1 |
71,684,699 (GRCm39) |
splice site |
probably benign |
|
IGL01311:Fn1
|
APN |
1 |
71,667,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01338:Fn1
|
APN |
1 |
71,665,369 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01353:Fn1
|
APN |
1 |
71,626,098 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01674:Fn1
|
APN |
1 |
71,645,900 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01701:Fn1
|
APN |
1 |
71,669,012 (GRCm39) |
splice site |
probably benign |
|
IGL01734:Fn1
|
APN |
1 |
71,658,644 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01788:Fn1
|
APN |
1 |
71,652,996 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02186:Fn1
|
APN |
1 |
71,677,693 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02398:Fn1
|
APN |
1 |
71,657,829 (GRCm39) |
splice site |
probably null |
|
IGL02425:Fn1
|
APN |
1 |
71,680,302 (GRCm39) |
splice site |
probably benign |
|
IGL02516:Fn1
|
APN |
1 |
71,676,482 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02593:Fn1
|
APN |
1 |
71,641,591 (GRCm39) |
missense |
probably benign |
|
IGL02651:Fn1
|
APN |
1 |
71,636,835 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02681:Fn1
|
APN |
1 |
71,658,641 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02890:Fn1
|
APN |
1 |
71,637,531 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02929:Fn1
|
APN |
1 |
71,634,821 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03036:Fn1
|
APN |
1 |
71,668,932 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03088:Fn1
|
APN |
1 |
71,653,197 (GRCm39) |
splice site |
probably null |
|
IGL03142:Fn1
|
APN |
1 |
71,676,455 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03172:Fn1
|
APN |
1 |
71,680,421 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03184:Fn1
|
APN |
1 |
71,648,656 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03212:Fn1
|
APN |
1 |
71,680,484 (GRCm39) |
nonsense |
probably null |
|
IGL03246:Fn1
|
APN |
1 |
71,663,455 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03367:Fn1
|
APN |
1 |
71,636,712 (GRCm39) |
missense |
probably benign |
0.27 |
depth
|
UTSW |
1 |
71,647,072 (GRCm39) |
missense |
probably damaging |
1.00 |
flooded
|
UTSW |
1 |
71,636,675 (GRCm39) |
missense |
probably benign |
0.01 |
R0684_Fn1_062
|
UTSW |
1 |
71,634,968 (GRCm39) |
splice site |
probably null |
|
series
|
UTSW |
1 |
71,634,945 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4514001:Fn1
|
UTSW |
1 |
71,667,615 (GRCm39) |
missense |
probably benign |
0.01 |
R0008:Fn1
|
UTSW |
1 |
71,634,879 (GRCm39) |
missense |
probably damaging |
0.98 |
R0112:Fn1
|
UTSW |
1 |
71,648,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R0138:Fn1
|
UTSW |
1 |
71,663,269 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0383:Fn1
|
UTSW |
1 |
71,636,844 (GRCm39) |
missense |
probably damaging |
0.99 |
R0386:Fn1
|
UTSW |
1 |
71,634,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R0648:Fn1
|
UTSW |
1 |
71,636,744 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0684:Fn1
|
UTSW |
1 |
71,634,968 (GRCm39) |
splice site |
probably null |
|
R1054:Fn1
|
UTSW |
1 |
71,625,373 (GRCm39) |
makesense |
probably null |
|
R1183:Fn1
|
UTSW |
1 |
71,625,404 (GRCm39) |
missense |
probably damaging |
0.98 |
R1405:Fn1
|
UTSW |
1 |
71,681,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R1405:Fn1
|
UTSW |
1 |
71,681,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R1414:Fn1
|
UTSW |
1 |
71,640,462 (GRCm39) |
splice site |
probably benign |
|
R1677:Fn1
|
UTSW |
1 |
71,636,814 (GRCm39) |
missense |
probably benign |
0.00 |
R1773:Fn1
|
UTSW |
1 |
71,676,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R1830:Fn1
|
UTSW |
1 |
71,663,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R1987:Fn1
|
UTSW |
1 |
71,690,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R1989:Fn1
|
UTSW |
1 |
71,690,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R2068:Fn1
|
UTSW |
1 |
71,639,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R2113:Fn1
|
UTSW |
1 |
71,665,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R2145:Fn1
|
UTSW |
1 |
71,645,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R2246:Fn1
|
UTSW |
1 |
71,667,694 (GRCm39) |
missense |
probably benign |
0.10 |
R2273:Fn1
|
UTSW |
1 |
71,653,102 (GRCm39) |
missense |
probably null |
1.00 |
R2274:Fn1
|
UTSW |
1 |
71,653,102 (GRCm39) |
missense |
probably null |
1.00 |
R2275:Fn1
|
UTSW |
1 |
71,653,102 (GRCm39) |
missense |
probably null |
1.00 |
R2303:Fn1
|
UTSW |
1 |
71,653,195 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2379:Fn1
|
UTSW |
1 |
71,688,443 (GRCm39) |
nonsense |
probably null |
|
R2382:Fn1
|
UTSW |
1 |
71,687,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R2567:Fn1
|
UTSW |
1 |
71,636,895 (GRCm39) |
nonsense |
probably null |
|
R2864:Fn1
|
UTSW |
1 |
71,641,578 (GRCm39) |
missense |
probably damaging |
0.99 |
R3154:Fn1
|
UTSW |
1 |
71,632,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R3837:Fn1
|
UTSW |
1 |
71,692,314 (GRCm39) |
splice site |
probably null |
|
R3844:Fn1
|
UTSW |
1 |
71,648,733 (GRCm39) |
missense |
possibly damaging |
0.61 |
R3886:Fn1
|
UTSW |
1 |
71,679,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R3887:Fn1
|
UTSW |
1 |
71,679,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R3888:Fn1
|
UTSW |
1 |
71,679,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R3889:Fn1
|
UTSW |
1 |
71,679,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R3905:Fn1
|
UTSW |
1 |
71,647,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R3906:Fn1
|
UTSW |
1 |
71,647,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R3907:Fn1
|
UTSW |
1 |
71,647,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R3909:Fn1
|
UTSW |
1 |
71,647,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R4611:Fn1
|
UTSW |
1 |
71,663,337 (GRCm39) |
nonsense |
probably null |
|
R4724:Fn1
|
UTSW |
1 |
71,687,307 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4732:Fn1
|
UTSW |
1 |
71,641,671 (GRCm39) |
splice site |
probably null |
|
R4733:Fn1
|
UTSW |
1 |
71,641,671 (GRCm39) |
splice site |
probably null |
|
R4809:Fn1
|
UTSW |
1 |
71,691,959 (GRCm39) |
intron |
probably benign |
|
R4839:Fn1
|
UTSW |
1 |
71,681,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R4915:Fn1
|
UTSW |
1 |
71,634,968 (GRCm39) |
splice site |
probably null |
|
R4917:Fn1
|
UTSW |
1 |
71,634,968 (GRCm39) |
splice site |
probably null |
|
R4918:Fn1
|
UTSW |
1 |
71,634,968 (GRCm39) |
splice site |
probably null |
|
R5002:Fn1
|
UTSW |
1 |
71,668,887 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5015:Fn1
|
UTSW |
1 |
71,665,336 (GRCm39) |
missense |
probably damaging |
0.98 |
R5022:Fn1
|
UTSW |
1 |
71,663,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R5109:Fn1
|
UTSW |
1 |
71,688,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R5267:Fn1
|
UTSW |
1 |
71,668,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R5323:Fn1
|
UTSW |
1 |
71,636,591 (GRCm39) |
missense |
probably benign |
0.09 |
R5333:Fn1
|
UTSW |
1 |
71,663,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R5631:Fn1
|
UTSW |
1 |
71,629,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R5644:Fn1
|
UTSW |
1 |
71,666,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R5754:Fn1
|
UTSW |
1 |
71,639,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R5807:Fn1
|
UTSW |
1 |
71,687,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R6053:Fn1
|
UTSW |
1 |
71,638,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R6133:Fn1
|
UTSW |
1 |
71,636,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R6186:Fn1
|
UTSW |
1 |
71,676,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R6270:Fn1
|
UTSW |
1 |
71,676,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R6332:Fn1
|
UTSW |
1 |
71,667,230 (GRCm39) |
missense |
probably benign |
0.01 |
R6431:Fn1
|
UTSW |
1 |
71,687,003 (GRCm39) |
splice site |
probably null |
|
R6571:Fn1
|
UTSW |
1 |
71,665,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R6596:Fn1
|
UTSW |
1 |
71,648,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R6862:Fn1
|
UTSW |
1 |
71,653,066 (GRCm39) |
missense |
probably benign |
0.43 |
R6898:Fn1
|
UTSW |
1 |
71,639,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R6984:Fn1
|
UTSW |
1 |
71,665,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R7107:Fn1
|
UTSW |
1 |
71,666,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R7121:Fn1
|
UTSW |
1 |
71,639,697 (GRCm39) |
intron |
probably benign |
|
R7127:Fn1
|
UTSW |
1 |
71,636,703 (GRCm39) |
missense |
probably benign |
0.16 |
R7194:Fn1
|
UTSW |
1 |
71,641,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R7274:Fn1
|
UTSW |
1 |
71,667,272 (GRCm39) |
missense |
probably benign |
|
R7285:Fn1
|
UTSW |
1 |
71,676,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R7426:Fn1
|
UTSW |
1 |
71,688,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R7453:Fn1
|
UTSW |
1 |
71,630,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R7508:Fn1
|
UTSW |
1 |
71,636,675 (GRCm39) |
missense |
probably benign |
0.01 |
R7724:Fn1
|
UTSW |
1 |
71,642,894 (GRCm39) |
missense |
probably benign |
0.02 |
R7848:Fn1
|
UTSW |
1 |
71,689,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R7992:Fn1
|
UTSW |
1 |
71,638,825 (GRCm39) |
missense |
probably benign |
0.34 |
R8036:Fn1
|
UTSW |
1 |
71,629,310 (GRCm39) |
nonsense |
probably null |
|
R8077:Fn1
|
UTSW |
1 |
71,651,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R8175:Fn1
|
UTSW |
1 |
71,638,824 (GRCm39) |
missense |
probably damaging |
1.00 |
R8177:Fn1
|
UTSW |
1 |
71,648,746 (GRCm39) |
missense |
probably benign |
|
R8212:Fn1
|
UTSW |
1 |
71,682,064 (GRCm39) |
missense |
probably benign |
0.01 |
R8322:Fn1
|
UTSW |
1 |
71,667,618 (GRCm39) |
missense |
probably benign |
0.04 |
R8745:Fn1
|
UTSW |
1 |
71,676,528 (GRCm39) |
missense |
probably benign |
0.00 |
R8780:Fn1
|
UTSW |
1 |
71,682,308 (GRCm39) |
missense |
probably benign |
0.00 |
R8805:Fn1
|
UTSW |
1 |
71,644,239 (GRCm39) |
missense |
probably benign |
0.27 |
R8927:Fn1
|
UTSW |
1 |
71,638,535 (GRCm39) |
missense |
probably benign |
0.16 |
R8928:Fn1
|
UTSW |
1 |
71,638,535 (GRCm39) |
missense |
probably benign |
0.16 |
R8928:Fn1
|
UTSW |
1 |
71,641,777 (GRCm39) |
intron |
probably benign |
|
R8989:Fn1
|
UTSW |
1 |
71,663,446 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8991:Fn1
|
UTSW |
1 |
71,676,491 (GRCm39) |
missense |
probably benign |
0.05 |
R9095:Fn1
|
UTSW |
1 |
71,647,149 (GRCm39) |
missense |
probably null |
0.02 |
R9455:Fn1
|
UTSW |
1 |
71,647,112 (GRCm39) |
missense |
probably benign |
|
R9589:Fn1
|
UTSW |
1 |
71,668,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R9631:Fn1
|
UTSW |
1 |
71,625,387 (GRCm39) |
missense |
probably benign |
0.01 |
R9645:Fn1
|
UTSW |
1 |
71,667,629 (GRCm39) |
missense |
probably benign |
0.35 |
R9723:Fn1
|
UTSW |
1 |
71,663,369 (GRCm39) |
missense |
possibly damaging |
0.95 |
X0023:Fn1
|
UTSW |
1 |
71,637,532 (GRCm39) |
critical splice donor site |
probably null |
|
Z1088:Fn1
|
UTSW |
1 |
71,688,451 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fn1
|
UTSW |
1 |
71,636,570 (GRCm39) |
missense |
probably benign |
0.10 |
|