Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankzf1 |
T |
C |
1: 75,169,312 (GRCm39) |
S73P |
probably benign |
Het |
Camsap3 |
T |
C |
8: 3,653,913 (GRCm39) |
Y517H |
probably damaging |
Het |
Catsperg1 |
C |
T |
7: 28,894,910 (GRCm39) |
M562I |
possibly damaging |
Het |
Ccdc18 |
A |
G |
5: 108,283,310 (GRCm39) |
D7G |
probably benign |
Het |
Ccdc65 |
A |
C |
15: 98,606,973 (GRCm39) |
N60T |
probably damaging |
Het |
Cemip2 |
G |
A |
19: 21,801,207 (GRCm39) |
D775N |
possibly damaging |
Het |
Col19a1 |
A |
G |
1: 24,365,054 (GRCm39) |
|
probably benign |
Het |
Ddx6 |
T |
C |
9: 44,524,194 (GRCm39) |
|
probably benign |
Het |
Dync1i1 |
G |
A |
6: 5,966,821 (GRCm39) |
|
probably null |
Het |
Eml6 |
T |
C |
11: 29,699,959 (GRCm39) |
N1726D |
probably benign |
Het |
Exosc10 |
T |
C |
4: 148,660,640 (GRCm39) |
S706P |
probably damaging |
Het |
Galntl6 |
T |
C |
8: 58,257,306 (GRCm39) |
E477G |
probably benign |
Het |
Gatd1 |
T |
G |
7: 140,990,951 (GRCm39) |
Q65H |
possibly damaging |
Het |
Hectd4 |
T |
A |
5: 121,503,116 (GRCm39) |
Y4362N |
possibly damaging |
Het |
Lag3 |
A |
G |
6: 124,882,434 (GRCm39) |
L354S |
probably benign |
Het |
Lrp1 |
A |
C |
10: 127,376,091 (GRCm39) |
V4342G |
probably benign |
Het |
Rap1gds1 |
T |
C |
3: 138,651,517 (GRCm39) |
I491V |
probably benign |
Het |
Scrib |
A |
G |
15: 75,937,973 (GRCm39) |
L291P |
probably damaging |
Het |
Shoc2 |
T |
C |
19: 54,019,525 (GRCm39) |
Y523H |
probably benign |
Het |
Slc47a2 |
C |
T |
11: 61,198,366 (GRCm39) |
G443E |
probably damaging |
Het |
Smarca2 |
T |
A |
19: 26,654,024 (GRCm39) |
|
probably benign |
Het |
Stra6l |
C |
T |
4: 45,885,278 (GRCm39) |
T582M |
possibly damaging |
Het |
Tmem144 |
G |
A |
3: 79,734,929 (GRCm39) |
T163I |
probably benign |
Het |
Tnfrsf17 |
T |
C |
16: 11,137,622 (GRCm39) |
Y120H |
probably damaging |
Het |
Tspan3 |
G |
T |
9: 56,053,800 (GRCm39) |
Q184K |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,628,270 (GRCm39) |
V14630D |
possibly damaging |
Het |
Zfp236 |
T |
A |
18: 82,642,584 (GRCm39) |
N1054I |
probably benign |
Het |
|
Other mutations in Fcamr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00840:Fcamr
|
APN |
1 |
130,740,951 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
|