| Other mutations in this stock |
Total: 60 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abhd17a |
A |
T |
10: 80,421,534 (GRCm39) |
Y145* |
probably null |
Het |
| Afdn |
T |
G |
17: 14,108,350 (GRCm39) |
I1291S |
probably benign |
Het |
| Arfgap3 |
T |
G |
15: 83,191,127 (GRCm39) |
I16L |
possibly damaging |
Het |
| Bbs12 |
T |
A |
3: 37,373,343 (GRCm39) |
H45Q |
possibly damaging |
Het |
| Brpf3 |
T |
C |
17: 29,043,022 (GRCm39) |
L1021P |
possibly damaging |
Het |
| Cep170 |
A |
G |
1: 176,596,903 (GRCm39) |
S485P |
possibly damaging |
Het |
| Cgref1 |
A |
T |
5: 31,090,937 (GRCm39) |
N292K |
probably damaging |
Het |
| Chst3 |
A |
T |
10: 60,022,261 (GRCm39) |
Y195* |
probably null |
Het |
| Clmn |
T |
C |
12: 104,740,782 (GRCm39) |
Y125C |
probably damaging |
Het |
| Col13a1 |
A |
G |
10: 61,729,692 (GRCm39) |
|
probably null |
Het |
| Cpeb3 |
A |
T |
19: 37,002,348 (GRCm39) |
I688N |
probably damaging |
Het |
| Cpn2 |
A |
T |
16: 30,079,647 (GRCm39) |
L18H |
probably benign |
Het |
| Crybg3 |
T |
A |
16: 59,375,542 (GRCm39) |
H1904L |
possibly damaging |
Het |
| Csde1 |
C |
T |
3: 102,951,155 (GRCm39) |
P249S |
probably damaging |
Het |
| Dcaf1 |
T |
C |
9: 106,721,339 (GRCm39) |
L377P |
probably damaging |
Het |
| Dmwd |
A |
T |
7: 18,815,054 (GRCm39) |
K568M |
probably damaging |
Het |
| Dsg2 |
T |
C |
18: 20,712,134 (GRCm39) |
I90T |
probably damaging |
Het |
| Dytn |
A |
G |
1: 63,680,281 (GRCm39) |
I426T |
probably damaging |
Het |
| Edc4 |
G |
A |
8: 106,613,943 (GRCm39) |
|
probably null |
Het |
| Elac1 |
G |
T |
18: 73,871,985 (GRCm39) |
Q337K |
probably benign |
Het |
| Exd2 |
G |
T |
12: 80,536,185 (GRCm39) |
A272S |
probably damaging |
Het |
| F13b |
A |
G |
1: 139,435,853 (GRCm39) |
I220V |
possibly damaging |
Het |
| Fblim1 |
G |
T |
4: 141,310,435 (GRCm39) |
R276S |
possibly damaging |
Het |
| Frem1 |
A |
T |
4: 82,877,576 (GRCm39) |
F1334I |
possibly damaging |
Het |
| H2-T23 |
T |
A |
17: 36,343,249 (GRCm39) |
I43F |
possibly damaging |
Het |
| Hp1bp3 |
G |
A |
4: 137,956,043 (GRCm39) |
G202D |
probably damaging |
Het |
| Kdm5b |
A |
G |
1: 134,536,675 (GRCm39) |
M632V |
probably damaging |
Het |
| Klra5 |
T |
A |
6: 129,885,830 (GRCm39) |
S20C |
probably damaging |
Het |
| Lancl1 |
A |
T |
1: 67,046,074 (GRCm39) |
C276S |
probably damaging |
Het |
| Lect2 |
A |
G |
13: 56,690,520 (GRCm39) |
*152Q |
probably null |
Het |
| Maff |
C |
A |
15: 79,241,658 (GRCm39) |
S25* |
probably null |
Het |
| Mtr |
A |
G |
13: 12,262,263 (GRCm39) |
L171P |
probably damaging |
Het |
| Ndufs1 |
A |
T |
1: 63,202,855 (GRCm39) |
Y236* |
probably null |
Het |
| Neb |
A |
C |
2: 52,134,165 (GRCm39) |
Y3273D |
probably damaging |
Het |
| Nup133 |
A |
T |
8: 124,673,333 (GRCm39) |
I66K |
probably benign |
Het |
| Or4c110 |
T |
C |
2: 88,832,459 (GRCm39) |
M58V |
possibly damaging |
Het |
| Psmd14 |
A |
G |
2: 61,614,205 (GRCm39) |
Y200C |
probably damaging |
Het |
| Ptgds |
T |
C |
2: 25,359,622 (GRCm39) |
T22A |
probably benign |
Het |
| Ptk2b |
T |
A |
14: 66,411,344 (GRCm39) |
|
probably benign |
Het |
| Pum3 |
G |
A |
19: 27,398,713 (GRCm39) |
T279M |
probably damaging |
Het |
| Rabl6 |
C |
T |
2: 25,474,868 (GRCm39) |
G614D |
probably benign |
Het |
| Ripk3 |
T |
C |
14: 56,024,796 (GRCm39) |
D128G |
probably benign |
Het |
| Serinc4 |
A |
T |
2: 121,270,039 (GRCm39) |
|
probably benign |
Het |
| Slco1a8 |
T |
G |
6: 141,954,333 (GRCm39) |
I47L |
possibly damaging |
Het |
| Sorbs2 |
T |
C |
8: 46,235,902 (GRCm39) |
S322P |
probably benign |
Het |
| Spmap2l |
A |
C |
5: 77,164,197 (GRCm39) |
K67Q |
possibly damaging |
Het |
| Srebf1 |
A |
T |
11: 60,111,284 (GRCm39) |
I29N |
possibly damaging |
Het |
| Stk38l |
T |
C |
6: 146,670,372 (GRCm39) |
L238S |
probably damaging |
Het |
| Supt20 |
T |
A |
3: 54,616,723 (GRCm39) |
C298* |
probably null |
Het |
| Tbc1d19 |
A |
G |
5: 54,054,389 (GRCm39) |
D459G |
probably damaging |
Het |
| Ulk2 |
A |
T |
11: 61,725,660 (GRCm39) |
L139M |
probably damaging |
Het |
| Unc13b |
A |
G |
4: 43,235,249 (GRCm39) |
N3279S |
probably damaging |
Het |
| Ush2a |
A |
G |
1: 188,596,818 (GRCm39) |
R3853G |
possibly damaging |
Het |
| Usp7 |
C |
T |
16: 8,556,078 (GRCm39) |
M24I |
probably benign |
Het |
| Vil1 |
A |
G |
1: 74,458,771 (GRCm39) |
T131A |
probably damaging |
Het |
| Vmn2r2 |
C |
T |
3: 64,024,321 (GRCm39) |
M753I |
probably benign |
Het |
| Vmn2r74 |
A |
T |
7: 85,601,900 (GRCm39) |
Y579* |
probably null |
Het |
| Zdhhc3 |
A |
T |
9: 122,929,582 (GRCm39) |
Y18N |
probably damaging |
Het |
| Zfp609 |
C |
T |
9: 65,609,927 (GRCm39) |
S1012N |
possibly damaging |
Het |
| Zfr2 |
A |
T |
10: 81,077,985 (GRCm39) |
M271L |
probably benign |
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 |
|
|
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 |
|
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