Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts20 |
T |
C |
15: 94,180,363 (GRCm39) |
Y1764C |
probably damaging |
Het |
Agbl3 |
T |
C |
6: 34,776,094 (GRCm39) |
V200A |
possibly damaging |
Het |
Akr1b10 |
T |
C |
6: 34,371,041 (GRCm39) |
S264P |
possibly damaging |
Het |
Camkmt |
T |
G |
17: 85,765,551 (GRCm39) |
L319* |
probably null |
Het |
Cdhr2 |
T |
C |
13: 54,867,965 (GRCm39) |
W513R |
probably damaging |
Het |
Cts8 |
T |
C |
13: 61,399,392 (GRCm39) |
Y189C |
probably damaging |
Het |
Cyp2d10 |
T |
A |
15: 82,288,691 (GRCm39) |
T264S |
probably benign |
Het |
Dbt |
G |
A |
3: 116,339,763 (GRCm39) |
G384S |
probably benign |
Het |
Dnah8 |
G |
A |
17: 31,009,915 (GRCm39) |
V3769M |
probably damaging |
Het |
Dnajc16 |
C |
A |
4: 141,495,314 (GRCm39) |
G468V |
probably damaging |
Het |
Eif3d |
A |
T |
15: 77,846,069 (GRCm39) |
N351K |
probably benign |
Het |
F5 |
T |
C |
1: 164,007,093 (GRCm39) |
M299T |
probably benign |
Het |
Heatr5b |
A |
G |
17: 79,072,866 (GRCm39) |
L1599P |
probably damaging |
Het |
Kl |
A |
T |
5: 150,904,252 (GRCm39) |
I335F |
possibly damaging |
Het |
Knop1 |
A |
G |
7: 118,452,021 (GRCm39) |
Y233H |
probably damaging |
Het |
Lhcgr |
T |
C |
17: 89,061,164 (GRCm39) |
|
probably benign |
Het |
Lypd11 |
A |
T |
7: 24,422,931 (GRCm39) |
L129H |
probably damaging |
Het |
Macrod2 |
A |
T |
2: 142,018,578 (GRCm39) |
N237I |
possibly damaging |
Het |
Myo7a |
T |
C |
7: 97,700,866 (GRCm39) |
S2168G |
probably benign |
Het |
Naxe |
T |
C |
3: 87,965,290 (GRCm39) |
I108V |
probably benign |
Het |
Ncbp1 |
T |
A |
4: 46,161,307 (GRCm39) |
W428R |
probably damaging |
Het |
Nxpe3 |
T |
C |
16: 55,664,595 (GRCm39) |
I542V |
probably damaging |
Het |
Phkb |
T |
A |
8: 86,684,216 (GRCm39) |
S424R |
probably benign |
Het |
Rgs20 |
C |
T |
1: 5,140,238 (GRCm39) |
V55I |
probably benign |
Het |
Ros1 |
T |
G |
10: 52,020,969 (GRCm39) |
T648P |
possibly damaging |
Het |
Rpgr |
T |
C |
X: 10,074,948 (GRCm39) |
I233V |
possibly damaging |
Het |
Slc25a31 |
T |
C |
3: 40,679,308 (GRCm39) |
S258P |
probably benign |
Het |
Soat1 |
A |
C |
1: 156,261,766 (GRCm39) |
V414G |
probably damaging |
Het |
St18 |
A |
T |
1: 6,903,818 (GRCm39) |
E693V |
probably damaging |
Het |
Svil |
T |
C |
18: 5,063,555 (GRCm39) |
V1029A |
probably benign |
Het |
Tnfaip3 |
C |
A |
10: 18,880,874 (GRCm39) |
V398L |
probably damaging |
Het |
Ubap1 |
A |
G |
4: 41,379,562 (GRCm39) |
T259A |
probably benign |
Het |
Wdr7 |
A |
G |
18: 64,060,398 (GRCm39) |
E1347G |
possibly damaging |
Het |
|
Other mutations in Fcamr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02880:Fcamr
|
APN |
1 |
130,741,071 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03199:Fcamr
|
APN |
1 |
130,740,655 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03392:Fcamr
|
APN |
1 |
130,728,685 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03398:Fcamr
|
APN |
1 |
130,730,985 (GRCm39) |
missense |
probably damaging |
0.97 |
R1101:Fcamr
|
UTSW |
1 |
130,742,223 (GRCm39) |
splice site |
probably null |
|
R1312:Fcamr
|
UTSW |
1 |
130,739,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R1351:Fcamr
|
UTSW |
1 |
130,740,757 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1387:Fcamr
|
UTSW |
1 |
130,732,379 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1475:Fcamr
|
UTSW |
1 |
130,742,221 (GRCm39) |
splice site |
probably null |
|
R1728:Fcamr
|
UTSW |
1 |
130,740,553 (GRCm39) |
missense |
probably benign |
0.41 |
R1728:Fcamr
|
UTSW |
1 |
130,742,334 (GRCm39) |
missense |
probably benign |
|
R1728:Fcamr
|
UTSW |
1 |
130,732,306 (GRCm39) |
missense |
probably benign |
0.06 |
R1728:Fcamr
|
UTSW |
1 |
130,732,364 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Fcamr
|
UTSW |
1 |
130,739,317 (GRCm39) |
missense |
probably benign |
|
R1728:Fcamr
|
UTSW |
1 |
130,740,366 (GRCm39) |
missense |
probably benign |
0.38 |
R1728:Fcamr
|
UTSW |
1 |
130,740,429 (GRCm39) |
missense |
probably benign |
|
R1728:Fcamr
|
UTSW |
1 |
130,740,475 (GRCm39) |
missense |
probably benign |
0.00 |
R1728:Fcamr
|
UTSW |
1 |
130,740,546 (GRCm39) |
missense |
probably benign |
0.02 |
R1729:Fcamr
|
UTSW |
1 |
130,742,334 (GRCm39) |
missense |
probably benign |
|
R1729:Fcamr
|
UTSW |
1 |
130,732,364 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Fcamr
|
UTSW |
1 |
130,739,317 (GRCm39) |
missense |
probably benign |
|
R1729:Fcamr
|
UTSW |
1 |
130,740,366 (GRCm39) |
missense |
probably benign |
0.38 |
R1729:Fcamr
|
UTSW |
1 |
130,740,429 (GRCm39) |
missense |
probably benign |
|
R1729:Fcamr
|
UTSW |
1 |
130,740,475 (GRCm39) |
missense |
probably benign |
0.00 |
R1729:Fcamr
|
UTSW |
1 |
130,740,546 (GRCm39) |
missense |
probably benign |
0.02 |
R1729:Fcamr
|
UTSW |
1 |
130,740,553 (GRCm39) |
missense |
probably benign |
0.41 |
R1730:Fcamr
|
UTSW |
1 |
130,740,366 (GRCm39) |
missense |
probably benign |
0.38 |
R1730:Fcamr
|
UTSW |
1 |
130,740,429 (GRCm39) |
missense |
probably benign |
|
R1730:Fcamr
|
UTSW |
1 |
130,740,475 (GRCm39) |
missense |
probably benign |
0.00 |
R1730:Fcamr
|
UTSW |
1 |
130,740,546 (GRCm39) |
missense |
probably benign |
0.02 |
R1730:Fcamr
|
UTSW |
1 |
130,740,553 (GRCm39) |
missense |
probably benign |
0.41 |
R1730:Fcamr
|
UTSW |
1 |
130,742,334 (GRCm39) |
missense |
probably benign |
|
R1730:Fcamr
|
UTSW |
1 |
130,739,317 (GRCm39) |
missense |
probably benign |
|
R1739:Fcamr
|
UTSW |
1 |
130,732,364 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Fcamr
|
UTSW |
1 |
130,739,317 (GRCm39) |
missense |
probably benign |
|
R1739:Fcamr
|
UTSW |
1 |
130,740,366 (GRCm39) |
missense |
probably benign |
0.38 |
R1739:Fcamr
|
UTSW |
1 |
130,740,429 (GRCm39) |
missense |
probably benign |
|
R1739:Fcamr
|
UTSW |
1 |
130,740,475 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Fcamr
|
UTSW |
1 |
130,740,546 (GRCm39) |
missense |
probably benign |
0.02 |
R1739:Fcamr
|
UTSW |
1 |
130,740,553 (GRCm39) |
missense |
probably benign |
0.41 |
R1739:Fcamr
|
UTSW |
1 |
130,742,334 (GRCm39) |
missense |
probably benign |
|
R1762:Fcamr
|
UTSW |
1 |
130,732,364 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Fcamr
|
UTSW |
1 |
130,739,317 (GRCm39) |
missense |
probably benign |
|
R1762:Fcamr
|
UTSW |
1 |
130,740,366 (GRCm39) |
missense |
probably benign |
0.38 |
R1762:Fcamr
|
UTSW |
1 |
130,740,429 (GRCm39) |
missense |
probably benign |
|
R1762:Fcamr
|
UTSW |
1 |
130,740,475 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Fcamr
|
UTSW |
1 |
130,740,546 (GRCm39) |
missense |
probably benign |
0.02 |
R1762:Fcamr
|
UTSW |
1 |
130,740,553 (GRCm39) |
missense |
probably benign |
0.41 |
R1762:Fcamr
|
UTSW |
1 |
130,742,334 (GRCm39) |
missense |
probably benign |
|
R1783:Fcamr
|
UTSW |
1 |
130,742,334 (GRCm39) |
missense |
probably benign |
|
R1783:Fcamr
|
UTSW |
1 |
130,740,553 (GRCm39) |
missense |
probably benign |
0.41 |
R1783:Fcamr
|
UTSW |
1 |
130,740,546 (GRCm39) |
missense |
probably benign |
0.02 |
R1783:Fcamr
|
UTSW |
1 |
130,740,475 (GRCm39) |
missense |
probably benign |
0.00 |
R1783:Fcamr
|
UTSW |
1 |
130,740,429 (GRCm39) |
missense |
probably benign |
|
R1783:Fcamr
|
UTSW |
1 |
130,740,366 (GRCm39) |
missense |
probably benign |
0.38 |
R1783:Fcamr
|
UTSW |
1 |
130,739,317 (GRCm39) |
missense |
probably benign |
|
R1783:Fcamr
|
UTSW |
1 |
130,732,364 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Fcamr
|
UTSW |
1 |
130,742,334 (GRCm39) |
missense |
probably benign |
|
R1784:Fcamr
|
UTSW |
1 |
130,740,553 (GRCm39) |
missense |
probably benign |
0.41 |
R1784:Fcamr
|
UTSW |
1 |
130,740,546 (GRCm39) |
missense |
probably benign |
0.02 |
R1784:Fcamr
|
UTSW |
1 |
130,740,475 (GRCm39) |
missense |
probably benign |
0.00 |
R1784:Fcamr
|
UTSW |
1 |
130,740,429 (GRCm39) |
missense |
probably benign |
|
R1784:Fcamr
|
UTSW |
1 |
130,740,366 (GRCm39) |
missense |
probably benign |
0.38 |
R1784:Fcamr
|
UTSW |
1 |
130,739,317 (GRCm39) |
missense |
probably benign |
|
R1784:Fcamr
|
UTSW |
1 |
130,732,364 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Fcamr
|
UTSW |
1 |
130,740,546 (GRCm39) |
missense |
probably benign |
0.02 |
R1785:Fcamr
|
UTSW |
1 |
130,740,475 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Fcamr
|
UTSW |
1 |
130,740,429 (GRCm39) |
missense |
probably benign |
|
R1785:Fcamr
|
UTSW |
1 |
130,740,366 (GRCm39) |
missense |
probably benign |
0.38 |
R1785:Fcamr
|
UTSW |
1 |
130,739,317 (GRCm39) |
missense |
probably benign |
|
R1785:Fcamr
|
UTSW |
1 |
130,732,364 (GRCm39) |
missense |
probably benign |
0.00 |
R1785:Fcamr
|
UTSW |
1 |
130,732,306 (GRCm39) |
missense |
probably benign |
0.06 |
R1785:Fcamr
|
UTSW |
1 |
130,742,334 (GRCm39) |
missense |
probably benign |
|
R1785:Fcamr
|
UTSW |
1 |
130,740,553 (GRCm39) |
missense |
probably benign |
0.41 |
R1793:Fcamr
|
UTSW |
1 |
130,739,284 (GRCm39) |
missense |
probably benign |
0.03 |
R2085:Fcamr
|
UTSW |
1 |
130,739,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R3937:Fcamr
|
UTSW |
1 |
130,732,313 (GRCm39) |
missense |
probably damaging |
0.97 |
R4529:Fcamr
|
UTSW |
1 |
130,732,313 (GRCm39) |
missense |
probably damaging |
0.99 |
R4624:Fcamr
|
UTSW |
1 |
130,730,999 (GRCm39) |
missense |
probably damaging |
0.99 |
R4822:Fcamr
|
UTSW |
1 |
130,740,423 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5055:Fcamr
|
UTSW |
1 |
130,739,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R5514:Fcamr
|
UTSW |
1 |
130,741,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R5807:Fcamr
|
UTSW |
1 |
130,739,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R6077:Fcamr
|
UTSW |
1 |
130,740,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R6200:Fcamr
|
UTSW |
1 |
130,730,927 (GRCm39) |
missense |
probably benign |
0.16 |
R6653:Fcamr
|
UTSW |
1 |
130,740,939 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7081:Fcamr
|
UTSW |
1 |
130,740,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R7362:Fcamr
|
UTSW |
1 |
130,741,760 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7828:Fcamr
|
UTSW |
1 |
130,739,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R7861:Fcamr
|
UTSW |
1 |
130,742,375 (GRCm39) |
missense |
probably benign |
|
R8188:Fcamr
|
UTSW |
1 |
130,730,665 (GRCm39) |
splice site |
probably null |
|
R8869:Fcamr
|
UTSW |
1 |
130,739,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R8907:Fcamr
|
UTSW |
1 |
130,740,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R9568:Fcamr
|
UTSW |
1 |
130,732,356 (GRCm39) |
missense |
probably damaging |
0.99 |
X0012:Fcamr
|
UTSW |
1 |
130,740,471 (GRCm39) |
missense |
probably benign |
0.09 |
|