Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankk1 |
T |
C |
9: 49,333,265 (GRCm39) |
|
probably benign |
Het |
Ano5 |
T |
A |
7: 51,237,454 (GRCm39) |
N759K |
possibly damaging |
Het |
Arhgef10 |
A |
G |
8: 15,033,898 (GRCm39) |
T1072A |
possibly damaging |
Het |
BC107364 |
T |
C |
3: 96,341,745 (GRCm39) |
T93A |
unknown |
Het |
Canx |
C |
T |
11: 50,201,217 (GRCm39) |
E97K |
possibly damaging |
Het |
Casp8ap2 |
T |
C |
4: 32,631,126 (GRCm39) |
L62P |
probably damaging |
Het |
Cbfa2t3 |
C |
T |
8: 123,364,725 (GRCm39) |
|
probably benign |
Het |
Cmklr2 |
A |
T |
1: 63,222,811 (GRCm39) |
|
probably null |
Het |
Cntnap1 |
T |
A |
11: 101,073,373 (GRCm39) |
I618N |
probably damaging |
Het |
Cox17 |
C |
G |
16: 38,167,542 (GRCm39) |
P27R |
probably damaging |
Het |
Ctnna3 |
A |
G |
10: 64,708,986 (GRCm39) |
E675G |
probably damaging |
Het |
Cul9 |
A |
G |
17: 46,837,575 (GRCm39) |
L990P |
probably damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Eif2d |
T |
C |
1: 131,092,464 (GRCm39) |
V374A |
probably damaging |
Het |
Fhdc1 |
T |
C |
3: 84,382,033 (GRCm39) |
|
probably benign |
Het |
Fryl |
T |
A |
5: 73,222,804 (GRCm39) |
I1926F |
probably benign |
Het |
Galnt4 |
A |
G |
10: 98,945,046 (GRCm39) |
D257G |
probably damaging |
Het |
Gatm |
A |
G |
2: 122,428,629 (GRCm39) |
V344A |
probably benign |
Het |
Gli1 |
T |
G |
10: 127,167,369 (GRCm39) |
Y628S |
probably damaging |
Het |
Gsdmc3 |
A |
C |
15: 63,732,063 (GRCm39) |
|
probably null |
Het |
Hap1 |
T |
C |
11: 100,246,828 (GRCm39) |
T26A |
probably benign |
Het |
Helz2 |
C |
T |
2: 180,876,895 (GRCm39) |
G1200S |
probably benign |
Het |
Insyn1 |
T |
C |
9: 58,406,288 (GRCm39) |
F66S |
probably damaging |
Het |
Iqgap2 |
C |
T |
13: 96,028,171 (GRCm39) |
|
probably null |
Het |
Itga3 |
T |
A |
11: 94,943,320 (GRCm39) |
I895F |
probably benign |
Het |
Klhl33 |
A |
T |
14: 51,130,230 (GRCm39) |
C421* |
probably null |
Het |
Klra2 |
T |
C |
6: 131,219,789 (GRCm39) |
T131A |
probably damaging |
Het |
Krt14 |
T |
C |
11: 100,094,949 (GRCm39) |
E426G |
possibly damaging |
Het |
Limd2 |
A |
G |
11: 106,049,568 (GRCm39) |
F107L |
probably damaging |
Het |
Lipo4 |
A |
T |
19: 33,477,469 (GRCm39) |
N318K |
possibly damaging |
Het |
Mab21l2 |
T |
G |
3: 86,454,316 (GRCm39) |
D228A |
probably damaging |
Het |
Moxd2 |
G |
A |
6: 40,861,901 (GRCm39) |
H224Y |
probably damaging |
Het |
Mpp4 |
T |
C |
1: 59,162,624 (GRCm39) |
Y521C |
possibly damaging |
Het |
Msto1 |
C |
T |
3: 88,818,297 (GRCm39) |
A317T |
probably damaging |
Het |
Mtmr4 |
T |
C |
11: 87,501,793 (GRCm39) |
S559P |
probably damaging |
Het |
Muc4 |
T |
A |
16: 32,576,783 (GRCm39) |
H2094Q |
unknown |
Het |
Ndufa11 |
C |
A |
17: 57,024,922 (GRCm39) |
T28K |
probably damaging |
Het |
Or2b4 |
A |
G |
17: 38,116,686 (GRCm39) |
T217A |
probably benign |
Het |
Or4f4b |
G |
T |
2: 111,314,623 (GRCm39) |
A283S |
probably damaging |
Het |
Orai2 |
C |
A |
5: 136,179,610 (GRCm39) |
R155L |
probably damaging |
Het |
Pde4c |
A |
G |
8: 71,202,005 (GRCm39) |
D582G |
possibly damaging |
Het |
Pde4dip |
T |
C |
3: 97,661,749 (GRCm39) |
E609G |
probably null |
Het |
Prune2 |
A |
G |
19: 17,097,109 (GRCm39) |
D871G |
possibly damaging |
Het |
Rbpms2 |
T |
A |
9: 65,538,121 (GRCm39) |
L4Q |
probably damaging |
Het |
Rhbg |
T |
C |
3: 88,154,765 (GRCm39) |
Y213C |
probably damaging |
Het |
Rplp0 |
T |
A |
5: 115,700,562 (GRCm39) |
N243K |
possibly damaging |
Het |
Rtp4 |
A |
T |
16: 23,431,963 (GRCm39) |
H165L |
possibly damaging |
Het |
Ryr2 |
C |
A |
13: 11,677,115 (GRCm39) |
M3245I |
probably benign |
Het |
Sh2b2 |
T |
A |
5: 136,260,968 (GRCm39) |
M83L |
possibly damaging |
Het |
Simc1 |
T |
C |
13: 54,689,347 (GRCm39) |
I284T |
probably damaging |
Het |
Skp2 |
C |
A |
15: 9,113,786 (GRCm39) |
G376C |
probably damaging |
Het |
Slc46a1 |
T |
C |
11: 78,359,471 (GRCm39) |
S368P |
possibly damaging |
Het |
St6galnac1 |
A |
G |
11: 116,659,933 (GRCm39) |
S127P |
probably benign |
Het |
Tatdn3 |
A |
G |
1: 190,785,073 (GRCm39) |
I192T |
possibly damaging |
Het |
Tmem25 |
C |
A |
9: 44,707,383 (GRCm39) |
V239F |
possibly damaging |
Het |
Tprkb |
A |
C |
6: 85,909,922 (GRCm39) |
|
probably benign |
Het |
Trappc10 |
A |
G |
10: 78,032,168 (GRCm39) |
V1040A |
probably benign |
Het |
Txnrd1 |
G |
A |
10: 82,719,744 (GRCm39) |
|
probably benign |
Het |
Uhrf1 |
A |
T |
17: 56,625,089 (GRCm39) |
K544M |
probably damaging |
Het |
Unc80 |
T |
A |
1: 66,629,386 (GRCm39) |
H1294Q |
possibly damaging |
Het |
Uspl1 |
T |
A |
5: 149,146,560 (GRCm39) |
I437K |
probably damaging |
Het |
Vmn1r232 |
A |
T |
17: 21,133,999 (GRCm39) |
N200K |
possibly damaging |
Het |
Vmn2r19 |
A |
T |
6: 123,312,795 (GRCm39) |
I622F |
probably damaging |
Het |
Znfx1 |
A |
G |
2: 166,897,730 (GRCm39) |
F398S |
probably damaging |
Het |
|
Other mutations in Cmya5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00489:Cmya5
|
APN |
13 |
93,229,628 (GRCm39) |
missense |
probably benign |
0.13 |
IGL00516:Cmya5
|
APN |
13 |
93,234,675 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL00654:Cmya5
|
APN |
13 |
93,230,669 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00948:Cmya5
|
APN |
13 |
93,227,544 (GRCm39) |
missense |
probably benign |
|
IGL00966:Cmya5
|
APN |
13 |
93,234,414 (GRCm39) |
missense |
probably benign |
0.33 |
IGL00988:Cmya5
|
APN |
13 |
93,234,441 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01106:Cmya5
|
APN |
13 |
93,221,120 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01331:Cmya5
|
APN |
13 |
93,233,454 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL01392:Cmya5
|
APN |
13 |
93,225,714 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01508:Cmya5
|
APN |
13 |
93,230,535 (GRCm39) |
missense |
probably benign |
|
IGL01679:Cmya5
|
APN |
13 |
93,201,828 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01749:Cmya5
|
APN |
13 |
93,225,807 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01861:Cmya5
|
APN |
13 |
93,226,256 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02021:Cmya5
|
APN |
13 |
93,231,057 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02034:Cmya5
|
APN |
13 |
93,221,043 (GRCm39) |
splice site |
probably benign |
|
IGL02103:Cmya5
|
APN |
13 |
93,228,635 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02174:Cmya5
|
APN |
13 |
93,185,415 (GRCm39) |
missense |
possibly damaging |
0.76 |
IGL02176:Cmya5
|
APN |
13 |
93,226,658 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02210:Cmya5
|
APN |
13 |
93,229,242 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02229:Cmya5
|
APN |
13 |
93,229,194 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02306:Cmya5
|
APN |
13 |
93,234,527 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02311:Cmya5
|
APN |
13 |
93,227,163 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02409:Cmya5
|
APN |
13 |
93,226,706 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02561:Cmya5
|
APN |
13 |
93,228,366 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02676:Cmya5
|
APN |
13 |
93,229,361 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02683:Cmya5
|
APN |
13 |
93,227,505 (GRCm39) |
nonsense |
probably null |
|
IGL02685:Cmya5
|
APN |
13 |
93,227,505 (GRCm39) |
nonsense |
probably null |
|
IGL02686:Cmya5
|
APN |
13 |
93,227,505 (GRCm39) |
nonsense |
probably null |
|
IGL02724:Cmya5
|
APN |
13 |
93,233,163 (GRCm39) |
missense |
probably benign |
|
IGL02727:Cmya5
|
APN |
13 |
93,234,753 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL02965:Cmya5
|
APN |
13 |
93,229,065 (GRCm39) |
missense |
probably benign |
0.41 |
IGL03079:Cmya5
|
APN |
13 |
93,234,209 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03144:Cmya5
|
APN |
13 |
93,227,376 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03253:Cmya5
|
APN |
13 |
93,227,778 (GRCm39) |
nonsense |
probably null |
|
IGL03336:Cmya5
|
APN |
13 |
93,230,013 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03138:Cmya5
|
UTSW |
13 |
93,201,850 (GRCm39) |
missense |
probably damaging |
1.00 |
P0023:Cmya5
|
UTSW |
13 |
93,225,854 (GRCm39) |
missense |
probably benign |
0.22 |
P4748:Cmya5
|
UTSW |
13 |
93,210,983 (GRCm39) |
splice site |
probably benign |
|
R0123:Cmya5
|
UTSW |
13 |
93,232,412 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0206:Cmya5
|
UTSW |
13 |
93,232,065 (GRCm39) |
missense |
probably damaging |
0.98 |
R0206:Cmya5
|
UTSW |
13 |
93,232,065 (GRCm39) |
missense |
probably damaging |
0.98 |
R0242:Cmya5
|
UTSW |
13 |
93,232,108 (GRCm39) |
missense |
probably benign |
|
R0242:Cmya5
|
UTSW |
13 |
93,232,108 (GRCm39) |
missense |
probably benign |
|
R0331:Cmya5
|
UTSW |
13 |
93,280,911 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0363:Cmya5
|
UTSW |
13 |
93,231,377 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0382:Cmya5
|
UTSW |
13 |
93,229,256 (GRCm39) |
missense |
probably benign |
0.06 |
R0416:Cmya5
|
UTSW |
13 |
93,226,364 (GRCm39) |
missense |
probably benign |
0.05 |
R0446:Cmya5
|
UTSW |
13 |
93,230,164 (GRCm39) |
missense |
probably benign |
|
R0457:Cmya5
|
UTSW |
13 |
93,232,095 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0673:Cmya5
|
UTSW |
13 |
93,226,505 (GRCm39) |
missense |
probably damaging |
1.00 |
R0674:Cmya5
|
UTSW |
13 |
93,229,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R0692:Cmya5
|
UTSW |
13 |
93,230,357 (GRCm39) |
nonsense |
probably null |
|
R0698:Cmya5
|
UTSW |
13 |
93,232,065 (GRCm39) |
missense |
probably damaging |
0.98 |
R1227:Cmya5
|
UTSW |
13 |
93,230,954 (GRCm39) |
missense |
probably damaging |
0.99 |
R1272:Cmya5
|
UTSW |
13 |
93,231,620 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1335:Cmya5
|
UTSW |
13 |
93,178,043 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1353:Cmya5
|
UTSW |
13 |
93,178,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R1354:Cmya5
|
UTSW |
13 |
93,228,566 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1458:Cmya5
|
UTSW |
13 |
93,201,835 (GRCm39) |
missense |
probably benign |
0.44 |
R1572:Cmya5
|
UTSW |
13 |
93,230,777 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1698:Cmya5
|
UTSW |
13 |
93,200,027 (GRCm39) |
missense |
probably benign |
0.27 |
R1735:Cmya5
|
UTSW |
13 |
93,226,297 (GRCm39) |
missense |
probably benign |
0.11 |
R1743:Cmya5
|
UTSW |
13 |
93,233,825 (GRCm39) |
missense |
probably benign |
0.33 |
R1750:Cmya5
|
UTSW |
13 |
93,232,171 (GRCm39) |
missense |
probably benign |
|
R1827:Cmya5
|
UTSW |
13 |
93,210,956 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2068:Cmya5
|
UTSW |
13 |
93,227,032 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2132:Cmya5
|
UTSW |
13 |
93,205,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R2216:Cmya5
|
UTSW |
13 |
93,230,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R2363:Cmya5
|
UTSW |
13 |
93,230,210 (GRCm39) |
missense |
probably benign |
0.15 |
R2497:Cmya5
|
UTSW |
13 |
93,234,513 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2509:Cmya5
|
UTSW |
13 |
93,230,066 (GRCm39) |
missense |
probably benign |
0.41 |
R2917:Cmya5
|
UTSW |
13 |
93,227,572 (GRCm39) |
nonsense |
probably null |
|
R2944:Cmya5
|
UTSW |
13 |
93,229,350 (GRCm39) |
nonsense |
probably null |
|
R3039:Cmya5
|
UTSW |
13 |
93,228,758 (GRCm39) |
missense |
probably benign |
0.12 |
R3078:Cmya5
|
UTSW |
13 |
93,185,435 (GRCm39) |
missense |
probably damaging |
0.99 |
R3708:Cmya5
|
UTSW |
13 |
93,231,874 (GRCm39) |
nonsense |
probably null |
|
R3717:Cmya5
|
UTSW |
13 |
93,228,995 (GRCm39) |
missense |
probably benign |
0.12 |
R3768:Cmya5
|
UTSW |
13 |
93,233,201 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3769:Cmya5
|
UTSW |
13 |
93,233,201 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3840:Cmya5
|
UTSW |
13 |
93,231,140 (GRCm39) |
missense |
probably damaging |
0.96 |
R3841:Cmya5
|
UTSW |
13 |
93,231,140 (GRCm39) |
missense |
probably damaging |
0.96 |
R3882:Cmya5
|
UTSW |
13 |
93,227,727 (GRCm39) |
missense |
probably benign |
0.07 |
R3888:Cmya5
|
UTSW |
13 |
93,230,164 (GRCm39) |
missense |
probably benign |
|
R3897:Cmya5
|
UTSW |
13 |
93,233,189 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3952:Cmya5
|
UTSW |
13 |
93,225,707 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4366:Cmya5
|
UTSW |
13 |
93,228,464 (GRCm39) |
missense |
probably benign |
0.36 |
R4471:Cmya5
|
UTSW |
13 |
93,228,833 (GRCm39) |
missense |
probably benign |
0.01 |
R4493:Cmya5
|
UTSW |
13 |
93,230,573 (GRCm39) |
missense |
probably benign |
|
R4495:Cmya5
|
UTSW |
13 |
93,230,573 (GRCm39) |
missense |
probably benign |
|
R4544:Cmya5
|
UTSW |
13 |
93,228,426 (GRCm39) |
nonsense |
probably null |
|
R4545:Cmya5
|
UTSW |
13 |
93,228,426 (GRCm39) |
nonsense |
probably null |
|
R4624:Cmya5
|
UTSW |
13 |
93,200,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R4648:Cmya5
|
UTSW |
13 |
93,230,336 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4824:Cmya5
|
UTSW |
13 |
93,230,082 (GRCm39) |
missense |
probably benign |
0.04 |
R4965:Cmya5
|
UTSW |
13 |
93,232,295 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4967:Cmya5
|
UTSW |
13 |
93,227,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R5101:Cmya5
|
UTSW |
13 |
93,228,111 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5133:Cmya5
|
UTSW |
13 |
93,229,880 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5139:Cmya5
|
UTSW |
13 |
93,232,569 (GRCm39) |
missense |
probably benign |
0.00 |
R5220:Cmya5
|
UTSW |
13 |
93,228,804 (GRCm39) |
missense |
probably damaging |
0.99 |
R5332:Cmya5
|
UTSW |
13 |
93,232,703 (GRCm39) |
missense |
probably damaging |
0.96 |
R5337:Cmya5
|
UTSW |
13 |
93,219,781 (GRCm39) |
missense |
probably benign |
0.28 |
R5356:Cmya5
|
UTSW |
13 |
93,199,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R5401:Cmya5
|
UTSW |
13 |
93,228,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R5438:Cmya5
|
UTSW |
13 |
93,231,707 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5604:Cmya5
|
UTSW |
13 |
93,229,271 (GRCm39) |
missense |
probably benign |
0.15 |
R5628:Cmya5
|
UTSW |
13 |
93,226,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R5666:Cmya5
|
UTSW |
13 |
93,182,457 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5687:Cmya5
|
UTSW |
13 |
93,234,684 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5695:Cmya5
|
UTSW |
13 |
93,182,374 (GRCm39) |
critical splice donor site |
probably null |
|
R5806:Cmya5
|
UTSW |
13 |
93,230,445 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5820:Cmya5
|
UTSW |
13 |
93,229,288 (GRCm39) |
missense |
probably benign |
0.04 |
R5872:Cmya5
|
UTSW |
13 |
93,233,943 (GRCm39) |
missense |
probably benign |
0.01 |
R5875:Cmya5
|
UTSW |
13 |
93,231,692 (GRCm39) |
missense |
probably benign |
0.13 |
R5896:Cmya5
|
UTSW |
13 |
93,182,373 (GRCm39) |
critical splice donor site |
probably null |
|
R5910:Cmya5
|
UTSW |
13 |
93,229,151 (GRCm39) |
missense |
probably damaging |
0.98 |
R5969:Cmya5
|
UTSW |
13 |
93,226,052 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6064:Cmya5
|
UTSW |
13 |
93,226,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R6081:Cmya5
|
UTSW |
13 |
93,281,021 (GRCm39) |
unclassified |
probably benign |
|
R6102:Cmya5
|
UTSW |
13 |
93,230,739 (GRCm39) |
missense |
probably benign |
|
R6117:Cmya5
|
UTSW |
13 |
93,231,674 (GRCm39) |
missense |
probably damaging |
0.98 |
R6188:Cmya5
|
UTSW |
13 |
93,233,784 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6188:Cmya5
|
UTSW |
13 |
93,229,952 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6219:Cmya5
|
UTSW |
13 |
93,230,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R6229:Cmya5
|
UTSW |
13 |
93,229,814 (GRCm39) |
missense |
probably benign |
0.41 |
R6346:Cmya5
|
UTSW |
13 |
93,228,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R6431:Cmya5
|
UTSW |
13 |
93,210,972 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6436:Cmya5
|
UTSW |
13 |
93,225,723 (GRCm39) |
missense |
probably damaging |
0.98 |
R6598:Cmya5
|
UTSW |
13 |
93,226,316 (GRCm39) |
missense |
probably benign |
0.05 |
R6649:Cmya5
|
UTSW |
13 |
93,234,533 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6652:Cmya5
|
UTSW |
13 |
93,229,547 (GRCm39) |
missense |
probably damaging |
0.99 |
R6652:Cmya5
|
UTSW |
13 |
93,229,403 (GRCm39) |
missense |
probably benign |
0.04 |
R6669:Cmya5
|
UTSW |
13 |
93,229,767 (GRCm39) |
missense |
probably benign |
0.03 |
R6881:Cmya5
|
UTSW |
13 |
93,226,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R6909:Cmya5
|
UTSW |
13 |
93,227,760 (GRCm39) |
missense |
probably benign |
0.04 |
R6933:Cmya5
|
UTSW |
13 |
93,231,644 (GRCm39) |
missense |
probably benign |
0.03 |
R7021:Cmya5
|
UTSW |
13 |
93,230,063 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7022:Cmya5
|
UTSW |
13 |
93,205,786 (GRCm39) |
critical splice donor site |
probably null |
|
R7068:Cmya5
|
UTSW |
13 |
93,229,205 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7087:Cmya5
|
UTSW |
13 |
93,227,483 (GRCm39) |
missense |
probably benign |
0.00 |
R7088:Cmya5
|
UTSW |
13 |
93,228,372 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7126:Cmya5
|
UTSW |
13 |
93,226,448 (GRCm39) |
missense |
probably benign |
0.41 |
R7177:Cmya5
|
UTSW |
13 |
93,231,836 (GRCm39) |
missense |
probably benign |
0.00 |
R7188:Cmya5
|
UTSW |
13 |
93,182,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R7217:Cmya5
|
UTSW |
13 |
93,226,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R7278:Cmya5
|
UTSW |
13 |
93,232,208 (GRCm39) |
missense |
probably damaging |
0.96 |
R7293:Cmya5
|
UTSW |
13 |
93,229,305 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7332:Cmya5
|
UTSW |
13 |
93,229,061 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7375:Cmya5
|
UTSW |
13 |
93,228,169 (GRCm39) |
missense |
probably damaging |
0.97 |
R7386:Cmya5
|
UTSW |
13 |
93,205,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R7489:Cmya5
|
UTSW |
13 |
93,228,346 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7529:Cmya5
|
UTSW |
13 |
93,233,942 (GRCm39) |
missense |
probably benign |
0.02 |
R7552:Cmya5
|
UTSW |
13 |
93,205,820 (GRCm39) |
missense |
probably benign |
0.41 |
R7624:Cmya5
|
UTSW |
13 |
93,226,865 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7637:Cmya5
|
UTSW |
13 |
93,219,720 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7673:Cmya5
|
UTSW |
13 |
93,230,629 (GRCm39) |
missense |
probably benign |
0.13 |
R7753:Cmya5
|
UTSW |
13 |
93,234,680 (GRCm39) |
missense |
probably benign |
0.18 |
R7757:Cmya5
|
UTSW |
13 |
93,234,780 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7806:Cmya5
|
UTSW |
13 |
93,230,770 (GRCm39) |
missense |
probably benign |
0.00 |
R7825:Cmya5
|
UTSW |
13 |
93,234,136 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7878:Cmya5
|
UTSW |
13 |
93,226,265 (GRCm39) |
missense |
probably damaging |
0.98 |
R7892:Cmya5
|
UTSW |
13 |
93,232,865 (GRCm39) |
missense |
probably damaging |
0.96 |
R7952:Cmya5
|
UTSW |
13 |
93,233,512 (GRCm39) |
small deletion |
probably benign |
|
R8127:Cmya5
|
UTSW |
13 |
93,231,122 (GRCm39) |
missense |
probably damaging |
0.99 |
R8256:Cmya5
|
UTSW |
13 |
93,229,986 (GRCm39) |
missense |
possibly damaging |
0.62 |
R8339:Cmya5
|
UTSW |
13 |
93,228,142 (GRCm39) |
nonsense |
probably null |
|
R8446:Cmya5
|
UTSW |
13 |
93,230,336 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8553:Cmya5
|
UTSW |
13 |
93,230,304 (GRCm39) |
missense |
probably benign |
0.00 |
R8686:Cmya5
|
UTSW |
13 |
93,231,888 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8748:Cmya5
|
UTSW |
13 |
93,226,229 (GRCm39) |
missense |
probably damaging |
1.00 |
R8783:Cmya5
|
UTSW |
13 |
93,225,888 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8803:Cmya5
|
UTSW |
13 |
93,177,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Cmya5
|
UTSW |
13 |
93,200,048 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8937:Cmya5
|
UTSW |
13 |
93,232,840 (GRCm39) |
missense |
probably benign |
0.01 |
R8985:Cmya5
|
UTSW |
13 |
93,233,664 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9017:Cmya5
|
UTSW |
13 |
93,228,572 (GRCm39) |
missense |
probably benign |
0.03 |
R9087:Cmya5
|
UTSW |
13 |
93,233,711 (GRCm39) |
missense |
possibly damaging |
0.72 |
R9133:Cmya5
|
UTSW |
13 |
93,234,108 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9156:Cmya5
|
UTSW |
13 |
93,233,878 (GRCm39) |
missense |
unknown |
|
R9209:Cmya5
|
UTSW |
13 |
93,226,866 (GRCm39) |
missense |
probably benign |
0.45 |
R9222:Cmya5
|
UTSW |
13 |
93,230,579 (GRCm39) |
missense |
probably benign |
0.00 |
R9229:Cmya5
|
UTSW |
13 |
93,232,176 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9382:Cmya5
|
UTSW |
13 |
93,229,884 (GRCm39) |
missense |
probably benign |
|
R9385:Cmya5
|
UTSW |
13 |
93,230,880 (GRCm39) |
missense |
probably damaging |
0.99 |
R9418:Cmya5
|
UTSW |
13 |
93,226,209 (GRCm39) |
missense |
probably benign |
0.22 |
R9452:Cmya5
|
UTSW |
13 |
93,232,394 (GRCm39) |
missense |
probably benign |
|
R9492:Cmya5
|
UTSW |
13 |
93,177,822 (GRCm39) |
makesense |
probably null |
|
R9600:Cmya5
|
UTSW |
13 |
93,226,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R9712:Cmya5
|
UTSW |
13 |
93,201,881 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9742:Cmya5
|
UTSW |
13 |
93,231,935 (GRCm39) |
missense |
possibly damaging |
0.89 |
RF020:Cmya5
|
UTSW |
13 |
93,205,799 (GRCm39) |
missense |
possibly damaging |
0.56 |
X0028:Cmya5
|
UTSW |
13 |
93,233,195 (GRCm39) |
missense |
possibly damaging |
0.53 |
Z1088:Cmya5
|
UTSW |
13 |
93,200,087 (GRCm39) |
missense |
probably benign |
|
Z1176:Cmya5
|
UTSW |
13 |
93,233,298 (GRCm39) |
missense |
unknown |
|
Z1176:Cmya5
|
UTSW |
13 |
93,200,087 (GRCm39) |
missense |
probably benign |
|
Z1177:Cmya5
|
UTSW |
13 |
93,200,087 (GRCm39) |
missense |
probably benign |
|
|