Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
T |
A |
8: 41,207,671 (GRCm39) |
F312L |
probably benign |
Het |
Adprm |
A |
G |
11: 66,932,856 (GRCm39) |
F18L |
possibly damaging |
Het |
Ampd1 |
T |
G |
3: 103,006,981 (GRCm39) |
N735K |
possibly damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Atp1a4 |
T |
C |
1: 172,081,649 (GRCm39) |
M168V |
probably damaging |
Het |
Bcl6 |
G |
A |
16: 23,793,600 (GRCm39) |
H116Y |
probably damaging |
Het |
Bmpr2 |
T |
A |
1: 59,890,383 (GRCm39) |
N338K |
probably damaging |
Het |
Bms1 |
A |
T |
6: 118,381,224 (GRCm39) |
Y697* |
probably null |
Het |
Ccdc33 |
A |
C |
9: 58,025,918 (GRCm39) |
F37C |
probably damaging |
Het |
Ccdc60 |
T |
A |
5: 116,426,507 (GRCm39) |
Q30L |
probably benign |
Het |
Cndp1 |
C |
A |
18: 84,650,036 (GRCm39) |
R219L |
probably damaging |
Het |
Cstdc4 |
T |
C |
16: 36,006,837 (GRCm39) |
|
probably null |
Het |
Daam2 |
C |
A |
17: 49,783,550 (GRCm39) |
D627Y |
probably damaging |
Het |
Dffb |
T |
C |
4: 154,057,416 (GRCm39) |
D87G |
possibly damaging |
Het |
Dnah2 |
T |
G |
11: 69,388,708 (GRCm39) |
T892P |
possibly damaging |
Het |
Dqx1 |
A |
G |
6: 83,043,092 (GRCm39) |
T610A |
probably benign |
Het |
Dspp |
A |
T |
5: 104,324,926 (GRCm39) |
I430L |
possibly damaging |
Het |
Dytn |
T |
A |
1: 63,672,854 (GRCm39) |
K516N |
probably benign |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fmnl2 |
T |
A |
2: 52,993,773 (GRCm39) |
N389K |
possibly damaging |
Het |
Foxn1 |
T |
C |
11: 78,261,989 (GRCm39) |
K127E |
probably damaging |
Het |
Fpr-rs6 |
A |
G |
17: 20,402,608 (GRCm39) |
F251S |
probably damaging |
Het |
Frrs1 |
A |
G |
3: 116,672,088 (GRCm39) |
D62G |
probably damaging |
Het |
Fut10 |
T |
A |
8: 31,726,148 (GRCm39) |
V301D |
probably damaging |
Het |
Gk5 |
A |
G |
9: 96,059,470 (GRCm39) |
|
probably null |
Het |
Glipr1l1 |
T |
A |
10: 111,914,279 (GRCm39) |
N213K |
probably benign |
Het |
Gm1110 |
A |
G |
9: 26,793,162 (GRCm39) |
F538S |
probably benign |
Het |
Gm7347 |
T |
A |
5: 26,262,366 (GRCm39) |
T52S |
probably benign |
Het |
Gsap |
T |
C |
5: 21,427,406 (GRCm39) |
I178T |
probably damaging |
Het |
H1f9 |
C |
A |
11: 94,858,928 (GRCm39) |
N74K |
probably damaging |
Het |
Hcn1 |
A |
T |
13: 117,739,556 (GRCm39) |
Q106L |
unknown |
Het |
Isg20l2 |
G |
T |
3: 87,839,288 (GRCm39) |
L166F |
possibly damaging |
Het |
Kcnq3 |
T |
A |
15: 65,876,612 (GRCm39) |
E510D |
probably damaging |
Het |
Kif26b |
G |
T |
1: 178,755,895 (GRCm39) |
R2003L |
probably damaging |
Het |
Kiss1r |
T |
C |
10: 79,754,641 (GRCm39) |
V45A |
probably damaging |
Het |
Krt14 |
G |
A |
11: 100,098,032 (GRCm39) |
R84* |
probably null |
Het |
Mbd5 |
T |
C |
2: 49,148,208 (GRCm39) |
M806T |
possibly damaging |
Het |
Mdga1 |
A |
T |
17: 30,058,847 (GRCm39) |
I13N |
possibly damaging |
Het |
Mfsd4b5 |
T |
C |
10: 39,850,758 (GRCm39) |
K73E |
probably benign |
Het |
Mterf2 |
C |
T |
10: 84,955,596 (GRCm39) |
G343R |
probably benign |
Het |
Mto1 |
T |
A |
9: 78,368,903 (GRCm39) |
F522I |
probably benign |
Het |
Myo18b |
T |
C |
5: 112,937,923 (GRCm39) |
E1734G |
probably damaging |
Het |
Myoz1 |
T |
C |
14: 20,703,787 (GRCm39) |
T53A |
probably benign |
Het |
Naxd |
T |
C |
8: 11,563,032 (GRCm39) |
L324P |
probably damaging |
Het |
Nos1 |
T |
A |
5: 118,005,334 (GRCm39) |
V18D |
probably damaging |
Het |
Nova1 |
T |
C |
12: 46,863,738 (GRCm39) |
T71A |
unknown |
Het |
Or10v5 |
T |
C |
19: 11,805,482 (GRCm39) |
R303G |
probably benign |
Het |
Or10z1 |
A |
G |
1: 174,078,448 (GRCm39) |
L15S |
possibly damaging |
Het |
Or1e29 |
C |
G |
11: 73,668,007 (GRCm39) |
V49L |
probably benign |
Het |
Or2j6 |
T |
C |
7: 139,980,083 (GRCm39) |
D292G |
probably damaging |
Het |
Or52b1 |
A |
G |
7: 104,978,811 (GRCm39) |
V196A |
possibly damaging |
Het |
Otof |
T |
A |
5: 30,540,238 (GRCm39) |
Y981F |
probably damaging |
Het |
Peg10 |
C |
CTCA |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Pex1 |
A |
G |
5: 3,670,597 (GRCm39) |
K7E |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,120,946 (GRCm39) |
S73P |
possibly damaging |
Het |
Plxnb1 |
T |
A |
9: 108,929,498 (GRCm39) |
I118N |
possibly damaging |
Het |
Prcc |
T |
C |
3: 87,779,560 (GRCm39) |
D158G |
probably damaging |
Het |
Ptpn7 |
C |
A |
1: 135,066,877 (GRCm39) |
R245S |
possibly damaging |
Het |
Ptpre |
C |
T |
7: 135,270,861 (GRCm39) |
H346Y |
probably benign |
Het |
Pwp2 |
A |
G |
10: 78,018,527 (GRCm39) |
C86R |
probably benign |
Het |
Rfng |
T |
G |
11: 120,673,876 (GRCm39) |
D178A |
probably damaging |
Het |
Rhpn1 |
T |
C |
15: 75,580,090 (GRCm39) |
I51T |
probably damaging |
Het |
Rnasel |
G |
T |
1: 153,629,843 (GRCm39) |
E120* |
probably null |
Het |
Sall2 |
T |
G |
14: 52,553,112 (GRCm39) |
S26R |
possibly damaging |
Het |
Scn10a |
A |
G |
9: 119,451,987 (GRCm39) |
V1312A |
possibly damaging |
Het |
Sdk2 |
C |
A |
11: 113,684,587 (GRCm39) |
R1958L |
probably damaging |
Het |
Septin4 |
C |
T |
11: 87,458,043 (GRCm39) |
S139F |
possibly damaging |
Het |
Slc52a2 |
T |
A |
15: 76,424,751 (GRCm39) |
C330S |
probably damaging |
Het |
Smarca2 |
T |
A |
19: 26,668,788 (GRCm39) |
I987N |
possibly damaging |
Het |
Srrt |
A |
T |
5: 137,294,271 (GRCm39) |
Y486N |
probably damaging |
Het |
Stat5b |
A |
T |
11: 100,695,831 (GRCm39) |
N50K |
possibly damaging |
Het |
Strip2 |
T |
A |
6: 29,931,265 (GRCm39) |
D405E |
probably benign |
Het |
Tcstv6 |
T |
A |
13: 120,298,474 (GRCm39) |
|
probably null |
Het |
Tnc |
A |
T |
4: 63,924,739 (GRCm39) |
D986E |
probably damaging |
Het |
Tph2 |
T |
C |
10: 114,915,621 (GRCm39) |
N473S |
probably benign |
Het |
Tpp1 |
C |
T |
7: 105,401,232 (GRCm39) |
|
probably benign |
Het |
Trpm3 |
T |
C |
19: 22,689,076 (GRCm39) |
Y2H |
probably damaging |
Het |
Ttc21a |
A |
T |
9: 119,795,195 (GRCm39) |
E1072V |
probably damaging |
Het |
Zfat |
T |
C |
15: 68,050,762 (GRCm39) |
D753G |
probably damaging |
Het |
Zmym2 |
T |
A |
14: 57,159,051 (GRCm39) |
S609T |
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 |
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 |
|
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 |
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 |
|