| Other mutations in this stock |
Total: 79 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca13 |
T |
C |
11: 9,240,350 (GRCm39) |
S738P |
probably benign |
Het |
| Abi3bp |
C |
A |
16: 56,408,348 (GRCm39) |
P261Q |
probably damaging |
Het |
| Adam19 |
A |
G |
11: 46,018,105 (GRCm39) |
N389S |
probably damaging |
Het |
| Adgrv1 |
A |
T |
13: 81,637,196 (GRCm39) |
V3415D |
possibly damaging |
Het |
| Ankrd33 |
A |
T |
15: 101,017,432 (GRCm39) |
I282F |
probably damaging |
Het |
| Arhgap39 |
C |
T |
15: 76,619,383 (GRCm39) |
V734M |
probably damaging |
Het |
| Arsg |
T |
C |
11: 109,454,100 (GRCm39) |
|
probably null |
Het |
| Atp8b4 |
C |
T |
2: 126,245,301 (GRCm39) |
G283R |
probably benign |
Het |
| B3galnt2 |
T |
G |
13: 14,166,119 (GRCm39) |
L338* |
probably null |
Het |
| Cdc14a |
A |
T |
3: 116,216,296 (GRCm39) |
Y1* |
probably null |
Het |
| Ceacam16 |
T |
C |
7: 19,592,803 (GRCm39) |
E35G |
possibly damaging |
Het |
| Cfap46 |
T |
A |
7: 139,220,323 (GRCm39) |
D1244V |
possibly damaging |
Het |
| Chordc1 |
T |
C |
9: 18,223,274 (GRCm39) |
Y245H |
probably damaging |
Het |
| Col6a6 |
C |
A |
9: 105,579,469 (GRCm39) |
V1919F |
probably damaging |
Het |
| Colgalt1 |
T |
C |
8: 72,075,781 (GRCm39) |
V476A |
probably damaging |
Het |
| Cped1 |
T |
C |
6: 22,237,727 (GRCm39) |
C948R |
probably damaging |
Het |
| Cyfip2 |
T |
C |
11: 46,089,846 (GRCm39) |
D1189G |
probably damaging |
Het |
| Cyp27b1 |
T |
C |
10: 126,884,952 (GRCm39) |
Y72H |
possibly damaging |
Het |
| Dagla |
A |
G |
19: 10,248,378 (GRCm39) |
M94T |
probably benign |
Het |
| Dip2a |
A |
G |
10: 76,153,797 (GRCm39) |
S178P |
probably damaging |
Het |
| Dlec1 |
T |
C |
9: 118,967,858 (GRCm39) |
V1220A |
probably benign |
Het |
| Dpysl2 |
T |
C |
14: 67,105,840 (GRCm39) |
|
probably benign |
Het |
| E2f6 |
T |
C |
12: 16,868,884 (GRCm39) |
V69A |
probably benign |
Het |
| Fat3 |
T |
C |
9: 15,826,636 (GRCm39) |
T4439A |
probably benign |
Het |
| Gabrr2 |
G |
A |
4: 33,077,481 (GRCm39) |
V83M |
probably damaging |
Het |
| Gfral |
T |
C |
9: 76,100,485 (GRCm39) |
N318D |
probably benign |
Het |
| Gm5611 |
A |
T |
9: 16,942,073 (GRCm39) |
|
noncoding transcript |
Het |
| Gpat3 |
A |
T |
5: 101,041,046 (GRCm39) |
M369L |
probably benign |
Het |
| Grik5 |
T |
C |
7: 24,745,726 (GRCm39) |
D449G |
possibly damaging |
Het |
| Gucy2g |
T |
A |
19: 55,211,362 (GRCm39) |
T623S |
possibly damaging |
Het |
| H2-T22 |
T |
C |
17: 36,352,434 (GRCm39) |
T164A |
probably benign |
Het |
| Herc1 |
T |
A |
9: 66,404,881 (GRCm39) |
C4484S |
possibly damaging |
Het |
| Hira |
T |
C |
16: 18,766,164 (GRCm39) |
S659P |
probably damaging |
Het |
| Hoxa7 |
T |
C |
6: 52,194,307 (GRCm39) |
T27A |
possibly damaging |
Het |
| Hoxd1 |
T |
C |
2: 74,593,866 (GRCm39) |
S141P |
probably damaging |
Het |
| Kank1 |
C |
A |
19: 25,388,396 (GRCm39) |
Q690K |
probably benign |
Het |
| Kera |
A |
G |
10: 97,445,009 (GRCm39) |
K123E |
probably benign |
Het |
| Kifbp |
T |
C |
10: 62,395,106 (GRCm39) |
Y512C |
probably damaging |
Het |
| Lepr |
A |
C |
4: 101,592,874 (GRCm39) |
Y163S |
probably damaging |
Het |
| Leprotl1 |
T |
C |
8: 34,607,922 (GRCm39) |
I29V |
probably benign |
Het |
| Lrriq1 |
T |
G |
10: 102,997,620 (GRCm39) |
T1332P |
probably benign |
Het |
| Mrps15 |
A |
G |
4: 125,949,200 (GRCm39) |
K223E |
probably damaging |
Het |
| Mrps7 |
T |
A |
11: 115,497,811 (GRCm39) |
N225K |
probably benign |
Het |
| Nav3 |
T |
A |
10: 109,659,184 (GRCm39) |
D811V |
probably damaging |
Het |
| Ndst3 |
T |
A |
3: 123,342,587 (GRCm39) |
R741S |
probably damaging |
Het |
| Nos3 |
T |
C |
5: 24,575,131 (GRCm39) |
Y356H |
probably damaging |
Het |
| Nxpe3 |
A |
G |
16: 55,686,444 (GRCm39) |
V188A |
probably damaging |
Het |
| Or13n4 |
T |
C |
7: 106,423,317 (GRCm39) |
R139G |
probably benign |
Het |
| Or5p50 |
T |
A |
7: 107,422,578 (GRCm39) |
I33F |
probably benign |
Het |
| Or8j3b |
T |
C |
2: 86,205,487 (GRCm39) |
K90E |
possibly damaging |
Het |
| Pdia4 |
A |
T |
6: 47,773,695 (GRCm39) |
C551* |
probably null |
Het |
| Pex13 |
A |
G |
11: 23,605,513 (GRCm39) |
F239S |
probably damaging |
Het |
| Pigq |
A |
G |
17: 26,153,980 (GRCm39) |
M273T |
probably benign |
Het |
| Plppr2 |
C |
T |
9: 21,859,047 (GRCm39) |
P388L |
probably damaging |
Het |
| Polr3b |
C |
T |
10: 84,528,786 (GRCm39) |
Q737* |
probably null |
Het |
| Ppfibp1 |
T |
C |
6: 146,923,757 (GRCm39) |
|
probably null |
Het |
| Ppfibp2 |
C |
A |
7: 107,236,504 (GRCm39) |
D17E |
probably damaging |
Het |
| Pramel34 |
A |
T |
5: 93,785,545 (GRCm39) |
I245K |
probably benign |
Het |
| Prr35 |
T |
C |
17: 26,165,691 (GRCm39) |
D532G |
possibly damaging |
Het |
| Ptpn13 |
A |
G |
5: 103,691,325 (GRCm39) |
D1064G |
probably benign |
Het |
| Qtrt2 |
A |
T |
16: 43,692,018 (GRCm39) |
S168T |
probably damaging |
Het |
| Rbp3 |
T |
C |
14: 33,676,601 (GRCm39) |
V183A |
probably benign |
Het |
| Shprh |
T |
C |
10: 11,062,655 (GRCm39) |
|
probably null |
Het |
| Slc39a10 |
T |
C |
1: 46,875,230 (GRCm39) |
H24R |
probably damaging |
Het |
| Slc7a13 |
A |
T |
4: 19,819,046 (GRCm39) |
H82L |
probably benign |
Het |
| Sptbn2 |
A |
G |
19: 4,782,569 (GRCm39) |
I502V |
probably benign |
Het |
| Syne2 |
C |
T |
12: 76,156,636 (GRCm39) |
R6811C |
probably damaging |
Het |
| Syt12 |
A |
G |
19: 4,506,911 (GRCm39) |
V78A |
probably benign |
Het |
| Tbck |
T |
A |
3: 132,543,772 (GRCm39) |
D874E |
probably benign |
Het |
| Tesc |
A |
T |
5: 118,184,394 (GRCm39) |
I25L |
probably damaging |
Het |
| Thoc5 |
T |
G |
11: 4,864,608 (GRCm39) |
D351E |
probably benign |
Het |
| Tor1aip1 |
A |
T |
1: 155,883,308 (GRCm39) |
M180K |
probably damaging |
Het |
| Trps1 |
T |
C |
15: 50,524,532 (GRCm39) |
S842G |
probably damaging |
Het |
| Unc79 |
A |
T |
12: 103,100,737 (GRCm39) |
T1858S |
probably damaging |
Het |
| Vmn1r193 |
T |
C |
13: 22,403,561 (GRCm39) |
T144A |
probably benign |
Het |
| Vwa8 |
T |
C |
14: 79,318,576 (GRCm39) |
F1046S |
probably benign |
Het |
| Wdr26 |
A |
T |
1: 181,019,340 (GRCm39) |
W346R |
probably damaging |
Het |
| Zfp740 |
T |
A |
15: 102,116,336 (GRCm39) |
V22E |
probably damaging |
Het |
| Zw10 |
C |
A |
9: 48,981,041 (GRCm39) |
S480R |
probably 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 |
|
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 |
|
|
R4756:Fn1
|
UTSW |
1 |
71,629,967 (GRCm39) |
missense |
probably damaging |
1.00 |
|
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 |
|
Incidental Mutation