Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
T |
G |
8: 111,768,206 (GRCm39) |
Y192* |
probably null |
Het |
Abcc6 |
T |
C |
7: 45,634,677 (GRCm39) |
Y1100C |
probably damaging |
Het |
Adamtsl2 |
T |
C |
2: 26,974,092 (GRCm39) |
W132R |
probably damaging |
Het |
Adgra2 |
T |
A |
8: 27,604,416 (GRCm39) |
V497E |
probably damaging |
Het |
Adtrp |
T |
G |
13: 41,981,813 (GRCm39) |
|
probably benign |
Het |
Alg9 |
T |
A |
9: 50,700,833 (GRCm39) |
L201Q |
possibly damaging |
Het |
Ap4e1 |
T |
A |
2: 126,856,121 (GRCm39) |
I84K |
probably damaging |
Het |
Atrnl1 |
T |
C |
19: 57,638,725 (GRCm39) |
S288P |
probably damaging |
Het |
Bltp1 |
T |
A |
3: 36,949,452 (GRCm39) |
L366Q |
possibly damaging |
Het |
Cacna1a |
A |
G |
8: 85,306,846 (GRCm39) |
D1367G |
probably damaging |
Het |
Card19 |
C |
T |
13: 49,358,727 (GRCm39) |
R82Q |
probably damaging |
Het |
Cep128 |
T |
C |
12: 91,292,372 (GRCm39) |
I226V |
possibly damaging |
Het |
Ces1f |
A |
C |
8: 93,994,633 (GRCm39) |
D259E |
probably benign |
Het |
Ckap5 |
T |
A |
2: 91,416,611 (GRCm39) |
M1072K |
probably benign |
Het |
Dcpp2 |
T |
A |
17: 24,119,468 (GRCm39) |
V94D |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,337,474 (GRCm39) |
D3209G |
possibly damaging |
Het |
Dsg1c |
A |
G |
18: 20,416,255 (GRCm39) |
T719A |
probably damaging |
Het |
Dsp |
G |
A |
13: 38,375,716 (GRCm39) |
W1167* |
probably null |
Het |
Eml5 |
T |
C |
12: 98,758,305 (GRCm39) |
I1874V |
probably benign |
Het |
Epg5 |
A |
G |
18: 78,003,926 (GRCm39) |
T645A |
probably damaging |
Het |
F2rl2 |
T |
C |
13: 95,837,621 (GRCm39) |
L222S |
probably damaging |
Het |
Fam114a1 |
T |
A |
5: 65,191,731 (GRCm39) |
C495S |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,163,537 (GRCm39) |
D2106E |
probably benign |
Het |
Fgf14 |
T |
A |
14: 124,913,936 (GRCm39) |
N65I |
probably benign |
Het |
Fip1l1 |
T |
C |
5: 74,755,763 (GRCm39) |
Y497H |
probably damaging |
Het |
Foxd2 |
T |
C |
4: 114,764,662 (GRCm39) |
T453A |
possibly damaging |
Het |
Galnt1 |
G |
T |
18: 24,404,647 (GRCm39) |
W328L |
probably damaging |
Het |
Gapt |
A |
G |
13: 110,490,372 (GRCm39) |
V97A |
possibly damaging |
Het |
Gatad1 |
A |
G |
5: 3,693,707 (GRCm39) |
V154A |
possibly damaging |
Het |
Gdf15 |
A |
G |
8: 71,084,202 (GRCm39) |
F21L |
probably benign |
Het |
Igdcc4 |
T |
C |
9: 65,029,182 (GRCm39) |
F273S |
possibly damaging |
Het |
Invs |
A |
T |
4: 48,421,725 (GRCm39) |
R786W |
possibly damaging |
Het |
Itfg1 |
T |
G |
8: 86,507,152 (GRCm39) |
E236A |
probably benign |
Het |
Jak3 |
A |
T |
8: 72,137,194 (GRCm39) |
I752F |
probably damaging |
Het |
Kcnip3 |
C |
A |
2: 127,306,985 (GRCm39) |
G144W |
probably damaging |
Het |
Kctd19 |
T |
C |
8: 106,109,598 (GRCm39) |
H925R |
probably benign |
Het |
Kdr |
C |
T |
5: 76,107,511 (GRCm39) |
A1011T |
probably damaging |
Het |
Kif13b |
C |
A |
14: 65,019,826 (GRCm39) |
H1398Q |
probably benign |
Het |
Lrp4 |
A |
T |
2: 91,307,864 (GRCm39) |
|
probably null |
Het |
Lrtm2 |
T |
C |
6: 119,297,846 (GRCm39) |
D65G |
probably benign |
Het |
Lyz1 |
A |
G |
10: 117,128,715 (GRCm39) |
L10P |
probably damaging |
Het |
Metap2 |
A |
T |
10: 93,706,046 (GRCm39) |
N245K |
probably damaging |
Het |
Mms19 |
T |
C |
19: 41,943,270 (GRCm39) |
D297G |
possibly damaging |
Het |
Mocs3 |
A |
G |
2: 168,073,573 (GRCm39) |
D340G |
possibly damaging |
Het |
Mtfr1l |
A |
G |
4: 134,256,436 (GRCm39) |
L243P |
probably damaging |
Het |
Mtss1 |
A |
G |
15: 58,842,897 (GRCm39) |
I105T |
probably damaging |
Het |
Myo18a |
T |
C |
11: 77,748,571 (GRCm39) |
S1967P |
probably damaging |
Het |
Ncor2 |
T |
C |
5: 125,100,585 (GRCm39) |
N2248S |
possibly damaging |
Het |
Nfatc2 |
T |
C |
2: 168,432,008 (GRCm39) |
D35G |
possibly damaging |
Het |
Nup210l |
T |
A |
3: 90,067,252 (GRCm39) |
M764K |
probably benign |
Het |
Or10a3n |
A |
G |
7: 108,492,948 (GRCm39) |
L222P |
probably damaging |
Het |
Otof |
T |
C |
5: 30,529,256 (GRCm39) |
S1753G |
probably damaging |
Het |
Otog |
G |
A |
7: 45,939,179 (GRCm39) |
V2070I |
probably benign |
Het |
Piezo2 |
A |
G |
18: 63,219,824 (GRCm39) |
V961A |
probably damaging |
Het |
Pofut1 |
C |
T |
2: 153,103,158 (GRCm39) |
S169L |
probably benign |
Het |
Ppp1r10 |
T |
A |
17: 36,240,335 (GRCm39) |
S542T |
possibly damaging |
Het |
Prpf8 |
T |
C |
11: 75,381,156 (GRCm39) |
Y219H |
possibly damaging |
Het |
Ptges3l |
T |
C |
11: 101,312,731 (GRCm39) |
D113G |
possibly damaging |
Het |
Pycr3 |
G |
A |
15: 75,790,647 (GRCm39) |
L71F |
probably benign |
Het |
Ramp3 |
A |
G |
11: 6,624,867 (GRCm39) |
K54E |
possibly damaging |
Het |
Rbpms |
C |
A |
8: 34,294,100 (GRCm39) |
Q214H |
possibly damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Robo4 |
C |
A |
9: 37,319,348 (GRCm39) |
D565E |
probably damaging |
Het |
S100a1 |
C |
T |
3: 90,418,641 (GRCm39) |
V58I |
probably benign |
Het |
Setx |
T |
A |
2: 29,070,104 (GRCm39) |
D2636E |
probably benign |
Het |
Sun2 |
A |
T |
15: 79,612,669 (GRCm39) |
V417E |
probably damaging |
Het |
Tbccd1 |
T |
C |
16: 22,660,519 (GRCm39) |
N99S |
probably benign |
Het |
Tex15 |
A |
G |
8: 34,064,893 (GRCm39) |
D1441G |
probably benign |
Het |
Tmc2 |
T |
A |
2: 130,089,896 (GRCm39) |
M627K |
probably damaging |
Het |
Trim32 |
A |
G |
4: 65,532,628 (GRCm39) |
Y395C |
probably benign |
Het |
Trpm2 |
A |
G |
10: 77,759,398 (GRCm39) |
Y1129H |
probably damaging |
Het |
Trpm8 |
A |
T |
1: 88,275,813 (GRCm39) |
R470S |
probably damaging |
Het |
Tsg101 |
G |
T |
7: 46,539,372 (GRCm39) |
D389E |
probably benign |
Het |
Ubn1 |
T |
C |
16: 4,882,406 (GRCm39) |
L46P |
probably damaging |
Het |
Ubr5 |
T |
C |
15: 37,997,419 (GRCm39) |
I1745V |
possibly damaging |
Het |
Usp20 |
T |
C |
2: 30,901,797 (GRCm39) |
Y521H |
probably benign |
Het |
Vmn1r159 |
A |
T |
7: 22,543,019 (GRCm39) |
H4Q |
probably null |
Het |
Vmn2r27 |
T |
A |
6: 124,177,491 (GRCm39) |
E504D |
probably benign |
Het |
Wdr72 |
A |
T |
9: 74,086,867 (GRCm39) |
I612F |
probably benign |
Het |
Zbtb8a |
T |
C |
4: 129,251,520 (GRCm39) |
H317R |
possibly damaging |
Het |
Zfp507 |
T |
C |
7: 35,494,315 (GRCm39) |
S243G |
probably damaging |
Het |
Zfp764 |
A |
G |
7: 127,005,419 (GRCm39) |
W73R |
probably damaging |
Het |
Zmym4 |
A |
T |
4: 126,819,632 (GRCm39) |
D90E |
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 |
|
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 |
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 |
|