Other mutations in this stock |
Total: 122 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310003L06Rik |
A |
G |
5: 88,112,335 (GRCm39) |
|
probably benign |
Het |
4930562C15Rik |
A |
C |
16: 4,653,835 (GRCm39) |
Q128P |
unknown |
Het |
Abcc3 |
T |
A |
11: 94,258,426 (GRCm39) |
K473M |
probably benign |
Het |
Acacb |
TGGGG |
TGGG |
5: 114,347,828 (GRCm39) |
|
probably null |
Het |
Adgrg7 |
C |
A |
16: 56,588,281 (GRCm39) |
A199S |
probably damaging |
Het |
Akap13 |
G |
T |
7: 75,261,182 (GRCm39) |
A1269S |
probably benign |
Het |
Aox3 |
A |
G |
1: 58,209,002 (GRCm39) |
H845R |
probably damaging |
Het |
Ap2b1 |
T |
A |
11: 83,215,587 (GRCm39) |
|
probably benign |
Het |
Atat1 |
A |
G |
17: 36,220,331 (GRCm39) |
S54P |
probably damaging |
Het |
Atp13a2 |
T |
A |
4: 140,732,327 (GRCm39) |
M864K |
probably damaging |
Het |
B3gnt3 |
G |
A |
8: 72,145,971 (GRCm39) |
T186M |
probably damaging |
Het |
Cars1 |
C |
A |
7: 143,146,211 (GRCm39) |
R71M |
probably damaging |
Het |
Castor2 |
G |
A |
5: 134,164,992 (GRCm39) |
C187Y |
probably damaging |
Het |
Ccdc157 |
A |
T |
11: 4,100,004 (GRCm39) |
V116E |
probably damaging |
Het |
Ccdc85a |
G |
A |
11: 28,384,151 (GRCm39) |
T408I |
probably benign |
Het |
Celf1 |
G |
T |
2: 90,840,791 (GRCm39) |
G353W |
probably damaging |
Het |
Celsr1 |
T |
A |
15: 85,916,168 (GRCm39) |
I602F |
possibly damaging |
Het |
Cenpb |
C |
T |
2: 131,021,226 (GRCm39) |
V191M |
probably damaging |
Het |
Cenpn |
G |
A |
8: 117,661,536 (GRCm39) |
|
probably null |
Het |
Cfap65 |
A |
C |
1: 74,946,850 (GRCm39) |
C1287G |
probably damaging |
Het |
Cnn3 |
A |
T |
3: 121,245,584 (GRCm39) |
E100V |
probably damaging |
Het |
Col4a4 |
G |
A |
1: 82,475,581 (GRCm39) |
R583C |
unknown |
Het |
Commd7 |
A |
C |
2: 153,463,586 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
T |
C |
15: 48,320,899 (GRCm39) |
T304A |
probably benign |
Het |
Cyp4a14 |
A |
T |
4: 115,348,588 (GRCm39) |
S325R |
probably damaging |
Het |
Dclk2 |
T |
C |
3: 86,827,353 (GRCm39) |
N42S |
probably benign |
Het |
Dmrta1 |
A |
T |
4: 89,576,946 (GRCm39) |
Q134L |
probably damaging |
Het |
Dnaaf3 |
T |
A |
7: 4,526,800 (GRCm39) |
I426L |
probably benign |
Het |
Dnah17 |
G |
A |
11: 117,924,573 (GRCm39) |
L3999F |
probably damaging |
Het |
Dock6 |
A |
G |
9: 21,757,814 (GRCm39) |
S97P |
probably benign |
Het |
Dsg1a |
T |
A |
18: 20,473,854 (GRCm39) |
S976T |
probably damaging |
Het |
Dstyk |
T |
A |
1: 132,377,222 (GRCm39) |
M29K |
probably null |
Het |
Eif3i |
A |
T |
4: 129,490,719 (GRCm39) |
H18Q |
probably benign |
Het |
Epm2a |
A |
G |
10: 11,219,426 (GRCm39) |
E71G |
probably benign |
Het |
Eps15l1 |
A |
T |
8: 73,140,712 (GRCm39) |
V260D |
probably benign |
Het |
Faf1 |
A |
G |
4: 109,568,042 (GRCm39) |
N34S |
probably damaging |
Het |
Fat3 |
A |
G |
9: 16,158,015 (GRCm39) |
|
probably null |
Het |
Fbxw10 |
T |
A |
11: 62,750,683 (GRCm39) |
I422N |
probably damaging |
Het |
Fcgbpl1 |
C |
T |
7: 27,854,899 (GRCm39) |
P1842S |
probably damaging |
Het |
Fkbp15 |
C |
A |
4: 62,246,136 (GRCm39) |
G431W |
probably damaging |
Het |
Flnb |
A |
C |
14: 7,873,376 (GRCm38) |
D224A |
probably benign |
Het |
Flnc |
G |
A |
6: 29,443,675 (GRCm39) |
V566M |
probably damaging |
Het |
Gli3 |
T |
A |
13: 15,900,134 (GRCm39) |
S1174T |
possibly damaging |
Het |
Glmn |
A |
T |
5: 107,726,321 (GRCm39) |
V93E |
probably damaging |
Het |
Glrx2 |
T |
C |
1: 143,620,842 (GRCm39) |
S74P |
possibly damaging |
Het |
Gm5422 |
G |
A |
10: 31,124,929 (GRCm39) |
|
noncoding transcript |
Het |
Gpi1 |
T |
C |
7: 33,905,339 (GRCm39) |
K362E |
probably damaging |
Het |
Gtpbp2 |
T |
C |
17: 46,472,128 (GRCm39) |
M21T |
probably benign |
Het |
Gxylt1 |
A |
G |
15: 93,142,851 (GRCm39) |
*405R |
probably null |
Het |
Heyl |
T |
C |
4: 123,139,876 (GRCm39) |
V145A |
probably damaging |
Het |
Hhipl1 |
A |
C |
12: 108,277,949 (GRCm39) |
E92D |
probably damaging |
Het |
Ifi207 |
A |
G |
1: 173,557,337 (GRCm39) |
F467S |
possibly damaging |
Het |
Ift70b |
G |
T |
2: 75,767,129 (GRCm39) |
H541Q |
probably damaging |
Het |
Igf2r |
A |
T |
17: 12,941,095 (GRCm39) |
I462N |
probably benign |
Het |
Inpp5b |
A |
T |
4: 124,678,961 (GRCm39) |
|
probably benign |
Het |
Kansl2 |
A |
G |
15: 98,427,278 (GRCm39) |
I201T |
probably damaging |
Het |
Kcnh8 |
T |
C |
17: 53,200,961 (GRCm39) |
V465A |
probably damaging |
Het |
Kcnu1 |
T |
A |
8: 26,341,928 (GRCm39) |
I91N |
probably damaging |
Het |
Kif5c |
T |
A |
2: 49,648,817 (GRCm39) |
|
probably benign |
Het |
Klrc3 |
T |
A |
6: 129,618,501 (GRCm39) |
Y94F |
probably benign |
Het |
Lgals3bp |
T |
A |
11: 118,284,113 (GRCm39) |
T489S |
probably benign |
Het |
Lmo2 |
T |
C |
2: 103,811,407 (GRCm39) |
Y147H |
probably damaging |
Het |
Lmtk2 |
C |
T |
5: 144,111,806 (GRCm39) |
T842I |
possibly damaging |
Het |
Magel2 |
A |
T |
7: 62,027,486 (GRCm39) |
H130L |
unknown |
Het |
Magi1 |
T |
C |
6: 93,674,255 (GRCm39) |
E951G |
probably damaging |
Het |
Mcm7 |
T |
C |
5: 138,167,364 (GRCm39) |
Q86R |
probably damaging |
Het |
Med12l |
G |
T |
3: 59,172,703 (GRCm39) |
|
probably null |
Het |
Morc2a |
A |
G |
11: 3,629,787 (GRCm39) |
E402G |
possibly damaging |
Het |
Mphosph8 |
T |
C |
14: 56,916,161 (GRCm39) |
C486R |
probably benign |
Het |
Mpo |
A |
G |
11: 87,688,187 (GRCm39) |
D282G |
possibly damaging |
Het |
Mtcl1 |
G |
T |
17: 66,650,618 (GRCm39) |
H1616N |
probably benign |
Het |
Myh10 |
A |
G |
11: 68,698,115 (GRCm39) |
|
probably benign |
Het |
Myh8 |
A |
G |
11: 67,183,702 (GRCm39) |
E777G |
probably damaging |
Het |
Nid1 |
A |
G |
13: 13,684,071 (GRCm39) |
H1186R |
probably benign |
Het |
Nppb |
T |
A |
4: 148,070,454 (GRCm39) |
S8T |
probably benign |
Het |
Nrp1 |
A |
T |
8: 129,224,997 (GRCm39) |
E782D |
probably damaging |
Het |
Ntrk3 |
G |
A |
7: 78,127,683 (GRCm39) |
|
probably benign |
Het |
Or1ak2 |
A |
G |
2: 36,827,704 (GRCm39) |
N191S |
probably benign |
Het |
Or1j13 |
A |
G |
2: 36,370,059 (GRCm39) |
S28P |
possibly damaging |
Het |
Or2f1 |
C |
A |
6: 42,721,069 (GRCm39) |
L33M |
possibly damaging |
Het |
Or5al5 |
A |
G |
2: 85,961,605 (GRCm39) |
V134A |
possibly damaging |
Het |
Or5b99 |
T |
A |
19: 12,976,402 (GRCm39) |
D17E |
probably benign |
Het |
Or6f1 |
C |
T |
7: 85,970,687 (GRCm39) |
V158M |
possibly damaging |
Het |
Osbpl6 |
T |
A |
2: 76,416,558 (GRCm39) |
I546K |
probably damaging |
Het |
Pard6g |
T |
C |
18: 80,160,523 (GRCm39) |
V212A |
probably damaging |
Het |
Pate6 |
T |
G |
9: 35,701,039 (GRCm39) |
|
probably benign |
Het |
Pdlim4 |
A |
G |
11: 53,954,563 (GRCm39) |
L48S |
possibly damaging |
Het |
Phactr3 |
T |
C |
2: 177,925,759 (GRCm39) |
F345L |
probably benign |
Het |
Plcb1 |
T |
A |
2: 135,167,587 (GRCm39) |
Y460* |
probably null |
Het |
Prcp |
T |
A |
7: 92,550,488 (GRCm39) |
V95D |
probably benign |
Het |
Rfwd3 |
A |
T |
8: 112,024,034 (GRCm39) |
V96E |
probably benign |
Het |
Ror1 |
A |
G |
4: 100,267,222 (GRCm39) |
N308D |
probably benign |
Het |
Sdccag8 |
C |
A |
1: 176,783,455 (GRCm39) |
Q655K |
probably damaging |
Het |
Senp1 |
T |
A |
15: 97,973,848 (GRCm39) |
T132S |
probably benign |
Het |
Skap1 |
T |
C |
11: 96,355,559 (GRCm39) |
I10T |
possibly damaging |
Het |
Slc9a4 |
T |
G |
1: 40,646,901 (GRCm39) |
|
probably null |
Het |
Smad2 |
T |
A |
18: 76,421,155 (GRCm39) |
C161* |
probably null |
Het |
Spata31d1a |
G |
T |
13: 59,848,857 (GRCm39) |
D1090E |
probably damaging |
Het |
Stard13 |
T |
C |
5: 150,968,633 (GRCm39) |
Y879C |
probably damaging |
Het |
Tdrd6 |
T |
C |
17: 43,935,724 (GRCm39) |
T1775A |
probably benign |
Het |
Tecpr1 |
T |
A |
5: 144,145,463 (GRCm39) |
T595S |
probably benign |
Het |
Terf1 |
A |
G |
1: 15,875,909 (GRCm39) |
E3G |
probably benign |
Het |
Tjp3 |
T |
A |
10: 81,113,888 (GRCm39) |
M457L |
possibly damaging |
Het |
Tnfrsf26 |
C |
T |
7: 143,171,577 (GRCm39) |
|
probably null |
Het |
Tor1aip1 |
A |
C |
1: 155,883,308 (GRCm39) |
M180R |
probably damaging |
Het |
Trabd2b |
A |
T |
4: 114,467,205 (GRCm39) |
Q478L |
probably benign |
Het |
Trim41 |
C |
A |
11: 48,698,419 (GRCm39) |
G516W |
probably damaging |
Het |
Ttc39a |
A |
G |
4: 109,299,903 (GRCm39) |
Y464C |
probably damaging |
Het |
Unc5a |
A |
G |
13: 55,138,896 (GRCm39) |
S92G |
probably damaging |
Het |
Unc5d |
A |
C |
8: 29,365,557 (GRCm39) |
S143A |
possibly damaging |
Het |
Usp34 |
A |
T |
11: 23,414,556 (GRCm39) |
H2833L |
possibly damaging |
Het |
Vps35l |
T |
C |
7: 118,393,798 (GRCm39) |
Y516H |
probably damaging |
Het |
Wdr17 |
T |
G |
8: 55,125,541 (GRCm39) |
K446N |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,338,392 (GRCm39) |
Q211L |
possibly damaging |
Het |
Xkr7 |
G |
A |
2: 152,894,816 (GRCm39) |
R256Q |
probably benign |
Het |
Zfp236 |
T |
C |
18: 82,639,429 (GRCm39) |
M1225V |
probably benign |
Het |
Zfp268 |
T |
A |
4: 145,350,803 (GRCm39) |
|
probably benign |
Het |
Zfp280d |
T |
C |
9: 72,215,287 (GRCm39) |
F133L |
probably damaging |
Het |
Zfp747l1 |
T |
C |
7: 126,986,107 (GRCm39) |
D8G |
probably benign |
Het |
Zfp758 |
A |
G |
17: 22,594,951 (GRCm39) |
H479R |
probably damaging |
Het |
Zfp827 |
A |
G |
8: 79,912,350 (GRCm39) |
N284S |
possibly damaging |
Het |
Zfyve26 |
T |
A |
12: 79,315,208 (GRCm39) |
I1423F |
possibly 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 |
R2088:Cmya5
|
UTSW |
13 |
93,229,320 (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 |
|
|