Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ascc3 |
A |
G |
10: 50,660,670 (GRCm38) |
N700D |
probably benign |
Het |
Babam2 |
G |
A |
5: 32,007,242 (GRCm38) |
V287M |
probably damaging |
Het |
Brip1 |
T |
C |
11: 86,189,801 (GRCm38) |
I146M |
possibly damaging |
Het |
Cacna1b |
C |
T |
2: 24,654,430 (GRCm38) |
R1248H |
probably damaging |
Het |
Ccdc88c |
G |
T |
12: 100,913,332 (GRCm38) |
S1843R |
possibly damaging |
Het |
Chaf1b |
G |
A |
16: 93,901,295 (GRCm38) |
A485T |
probably benign |
Het |
Dock7 |
T |
C |
4: 98,962,224 (GRCm38) |
R1594G |
probably damaging |
Het |
Fam122c |
G |
A |
X: 53,293,499 (GRCm38) |
R94H |
possibly damaging |
Het |
Fbxo41 |
A |
G |
6: 85,484,042 (GRCm38) |
I228T |
probably damaging |
Het |
Gm3739 |
T |
A |
14: 7,299,398 (GRCm38) |
K86* |
probably null |
Het |
Gm7173 |
A |
T |
X: 79,509,995 (GRCm38) |
N291K |
possibly damaging |
Het |
Mark2 |
A |
T |
19: 7,285,948 (GRCm38) |
D151E |
probably damaging |
Het |
Nop2 |
G |
T |
6: 125,133,552 (GRCm38) |
R47L |
probably damaging |
Het |
Nwd1 |
A |
T |
8: 72,670,951 (GRCm38) |
D606V |
probably damaging |
Het |
Olfr1132 |
T |
A |
2: 87,635,151 (GRCm38) |
I199L |
probably benign |
Het |
Pcbp1 |
T |
C |
6: 86,525,050 (GRCm38) |
N289S |
probably benign |
Het |
Plce1 |
T |
C |
19: 38,524,319 (GRCm38) |
S21P |
possibly damaging |
Het |
Ptpn18 |
T |
C |
1: 34,472,960 (GRCm38) |
L55P |
probably benign |
Het |
Rpl10l |
T |
C |
12: 66,283,738 (GRCm38) |
D207G |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,147,663 (GRCm38) |
C537R |
probably damaging |
Het |
Sec23b |
T |
A |
2: 144,578,366 (GRCm38) |
I450N |
possibly damaging |
Het |
Spem1 |
C |
A |
11: 69,821,805 (GRCm38) |
|
probably null |
Het |
Stxbp3-ps |
A |
T |
19: 9,559,110 (GRCm38) |
|
noncoding transcript |
Het |
Tmem38a |
C |
T |
8: 72,572,161 (GRCm38) |
P20S |
possibly damaging |
Het |
Tmod2 |
T |
C |
9: 75,592,584 (GRCm38) |
T129A |
probably benign |
Het |
Ttc28 |
A |
G |
5: 111,280,172 (GRCm38) |
T1845A |
probably benign |
Het |
Ubqlnl |
C |
T |
7: 104,149,718 (GRCm38) |
V191M |
probably benign |
Het |
Ush2a |
C |
T |
1: 188,864,625 (GRCm38) |
T3854M |
probably damaging |
Het |
Vmn2r72 |
T |
A |
7: 85,751,926 (GRCm38) |
H95L |
probably benign |
Het |
Xdh |
C |
A |
17: 73,898,344 (GRCm38) |
G1042V |
probably damaging |
Het |
Zfp105 |
T |
A |
9: 122,930,056 (GRCm38) |
V264E |
possibly damaging |
Het |
|
Other mutations in Speg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00838:Speg
|
APN |
1 |
75,410,390 (GRCm38) |
missense |
possibly damaging |
0.95 |
IGL00979:Speg
|
APN |
1 |
75,410,734 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL01122:Speg
|
APN |
1 |
75,410,035 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01293:Speg
|
APN |
1 |
75,388,102 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01304:Speg
|
APN |
1 |
75,428,197 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01351:Speg
|
APN |
1 |
75,411,276 (GRCm38) |
splice site |
probably benign |
|
IGL01473:Speg
|
APN |
1 |
75,428,285 (GRCm38) |
missense |
possibly damaging |
0.53 |
IGL01477:Speg
|
APN |
1 |
75,391,897 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01485:Speg
|
APN |
1 |
75,387,827 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01584:Speg
|
APN |
1 |
75,430,937 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01959:Speg
|
APN |
1 |
75,391,090 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02231:Speg
|
APN |
1 |
75,423,387 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02355:Speg
|
APN |
1 |
75,423,915 (GRCm38) |
missense |
possibly damaging |
0.49 |
IGL02362:Speg
|
APN |
1 |
75,423,915 (GRCm38) |
missense |
possibly damaging |
0.49 |
IGL03013:Speg
|
APN |
1 |
75,431,279 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL03168:Speg
|
APN |
1 |
75,388,187 (GRCm38) |
missense |
probably damaging |
1.00 |
H8562:Speg
|
UTSW |
1 |
75,415,597 (GRCm38) |
missense |
probably benign |
0.39 |
R0112:Speg
|
UTSW |
1 |
75,385,032 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0311:Speg
|
UTSW |
1 |
75,430,937 (GRCm38) |
missense |
probably damaging |
1.00 |
R0315:Speg
|
UTSW |
1 |
75,415,136 (GRCm38) |
missense |
possibly damaging |
0.88 |
R0393:Speg
|
UTSW |
1 |
75,423,924 (GRCm38) |
missense |
possibly damaging |
0.46 |
R0403:Speg
|
UTSW |
1 |
75,430,784 (GRCm38) |
splice site |
probably benign |
|
R0483:Speg
|
UTSW |
1 |
75,385,032 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0648:Speg
|
UTSW |
1 |
75,427,978 (GRCm38) |
missense |
probably benign |
|
R0683:Speg
|
UTSW |
1 |
75,429,118 (GRCm38) |
missense |
probably damaging |
1.00 |
R0800:Speg
|
UTSW |
1 |
75,423,489 (GRCm38) |
missense |
probably damaging |
1.00 |
R0815:Speg
|
UTSW |
1 |
75,415,392 (GRCm38) |
missense |
probably damaging |
1.00 |
R0835:Speg
|
UTSW |
1 |
75,375,674 (GRCm38) |
missense |
probably benign |
0.00 |
R0866:Speg
|
UTSW |
1 |
75,417,083 (GRCm38) |
missense |
probably damaging |
0.99 |
R0880:Speg
|
UTSW |
1 |
75,405,061 (GRCm38) |
missense |
probably damaging |
1.00 |
R1082:Speg
|
UTSW |
1 |
75,415,138 (GRCm38) |
missense |
possibly damaging |
0.94 |
R1140:Speg
|
UTSW |
1 |
75,429,095 (GRCm38) |
missense |
probably damaging |
1.00 |
R1252:Speg
|
UTSW |
1 |
75,427,095 (GRCm38) |
missense |
probably damaging |
1.00 |
R1301:Speg
|
UTSW |
1 |
75,401,501 (GRCm38) |
missense |
probably damaging |
1.00 |
R1348:Speg
|
UTSW |
1 |
75,422,872 (GRCm38) |
missense |
probably damaging |
0.99 |
R1388:Speg
|
UTSW |
1 |
75,430,460 (GRCm38) |
missense |
probably damaging |
0.99 |
R1465:Speg
|
UTSW |
1 |
75,428,484 (GRCm38) |
splice site |
probably benign |
|
R1505:Speg
|
UTSW |
1 |
75,375,542 (GRCm38) |
missense |
probably benign |
0.02 |
R1506:Speg
|
UTSW |
1 |
75,417,663 (GRCm38) |
missense |
probably benign |
0.03 |
R1531:Speg
|
UTSW |
1 |
75,401,222 (GRCm38) |
missense |
possibly damaging |
0.86 |
R1543:Speg
|
UTSW |
1 |
75,421,951 (GRCm38) |
missense |
probably damaging |
1.00 |
R1567:Speg
|
UTSW |
1 |
75,428,047 (GRCm38) |
missense |
probably benign |
|
R1630:Speg
|
UTSW |
1 |
75,422,977 (GRCm38) |
missense |
probably damaging |
1.00 |
R1667:Speg
|
UTSW |
1 |
75,410,549 (GRCm38) |
splice site |
probably benign |
|
R1673:Speg
|
UTSW |
1 |
75,411,163 (GRCm38) |
missense |
possibly damaging |
0.60 |
R1718:Speg
|
UTSW |
1 |
75,421,744 (GRCm38) |
missense |
possibly damaging |
0.87 |
R1718:Speg
|
UTSW |
1 |
75,417,863 (GRCm38) |
missense |
probably benign |
0.00 |
R1719:Speg
|
UTSW |
1 |
75,417,863 (GRCm38) |
missense |
probably benign |
0.00 |
R1759:Speg
|
UTSW |
1 |
75,401,162 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1861:Speg
|
UTSW |
1 |
75,389,005 (GRCm38) |
missense |
probably damaging |
1.00 |
R1874:Speg
|
UTSW |
1 |
75,423,906 (GRCm38) |
missense |
probably benign |
|
R1936:Speg
|
UTSW |
1 |
75,431,408 (GRCm38) |
missense |
possibly damaging |
0.93 |
R2192:Speg
|
UTSW |
1 |
75,417,727 (GRCm38) |
missense |
probably damaging |
1.00 |
R2204:Speg
|
UTSW |
1 |
75,430,477 (GRCm38) |
missense |
probably benign |
0.30 |
R2287:Speg
|
UTSW |
1 |
75,430,465 (GRCm38) |
missense |
possibly damaging |
0.76 |
R2696:Speg
|
UTSW |
1 |
75,406,926 (GRCm38) |
missense |
probably benign |
0.27 |
R2983:Speg
|
UTSW |
1 |
75,384,930 (GRCm38) |
missense |
possibly damaging |
0.83 |
R3110:Speg
|
UTSW |
1 |
75,422,682 (GRCm38) |
nonsense |
probably null |
|
R3112:Speg
|
UTSW |
1 |
75,422,682 (GRCm38) |
nonsense |
probably null |
|
R3154:Speg
|
UTSW |
1 |
75,401,542 (GRCm38) |
missense |
probably damaging |
1.00 |
R3720:Speg
|
UTSW |
1 |
75,426,782 (GRCm38) |
missense |
probably damaging |
1.00 |
R3983:Speg
|
UTSW |
1 |
75,422,547 (GRCm38) |
missense |
probably benign |
0.27 |
R4133:Speg
|
UTSW |
1 |
75,427,904 (GRCm38) |
missense |
probably benign |
|
R4564:Speg
|
UTSW |
1 |
75,391,834 (GRCm38) |
missense |
probably damaging |
1.00 |
R4577:Speg
|
UTSW |
1 |
75,415,395 (GRCm38) |
missense |
probably damaging |
1.00 |
R4858:Speg
|
UTSW |
1 |
75,421,735 (GRCm38) |
missense |
probably damaging |
1.00 |
R4953:Speg
|
UTSW |
1 |
75,423,864 (GRCm38) |
missense |
possibly damaging |
0.72 |
R4965:Speg
|
UTSW |
1 |
75,427,703 (GRCm38) |
missense |
probably damaging |
1.00 |
R4967:Speg
|
UTSW |
1 |
75,387,869 (GRCm38) |
missense |
probably damaging |
1.00 |
R5152:Speg
|
UTSW |
1 |
75,428,098 (GRCm38) |
missense |
possibly damaging |
0.92 |
R5156:Speg
|
UTSW |
1 |
75,428,087 (GRCm38) |
missense |
probably damaging |
0.99 |
R5371:Speg
|
UTSW |
1 |
75,431,393 (GRCm38) |
missense |
possibly damaging |
0.50 |
R5550:Speg
|
UTSW |
1 |
75,429,100 (GRCm38) |
missense |
probably damaging |
1.00 |
R5562:Speg
|
UTSW |
1 |
75,427,056 (GRCm38) |
missense |
probably damaging |
1.00 |
R5687:Speg
|
UTSW |
1 |
75,419,129 (GRCm38) |
splice site |
probably null |
|
R5985:Speg
|
UTSW |
1 |
75,406,684 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6004:Speg
|
UTSW |
1 |
75,415,603 (GRCm38) |
nonsense |
probably null |
|
R6038:Speg
|
UTSW |
1 |
75,418,459 (GRCm38) |
critical splice donor site |
probably null |
|
R6038:Speg
|
UTSW |
1 |
75,418,459 (GRCm38) |
critical splice donor site |
probably null |
|
R6143:Speg
|
UTSW |
1 |
75,414,387 (GRCm38) |
missense |
probably damaging |
1.00 |
R6265:Speg
|
UTSW |
1 |
75,406,679 (GRCm38) |
nonsense |
probably null |
|
R6347:Speg
|
UTSW |
1 |
75,426,875 (GRCm38) |
missense |
probably benign |
0.00 |
R6453:Speg
|
UTSW |
1 |
75,417,972 (GRCm38) |
missense |
probably benign |
0.06 |
R6505:Speg
|
UTSW |
1 |
75,429,523 (GRCm38) |
missense |
possibly damaging |
0.93 |
R6505:Speg
|
UTSW |
1 |
75,406,684 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6531:Speg
|
UTSW |
1 |
75,422,757 (GRCm38) |
missense |
probably benign |
0.03 |
R6566:Speg
|
UTSW |
1 |
75,388,463 (GRCm38) |
missense |
probably damaging |
1.00 |
R6747:Speg
|
UTSW |
1 |
75,410,395 (GRCm38) |
critical splice donor site |
probably null |
|
R6819:Speg
|
UTSW |
1 |
75,391,812 (GRCm38) |
missense |
possibly damaging |
0.56 |
R6821:Speg
|
UTSW |
1 |
75,417,903 (GRCm38) |
missense |
possibly damaging |
0.83 |
R6919:Speg
|
UTSW |
1 |
75,387,908 (GRCm38) |
nonsense |
probably null |
|
R6981:Speg
|
UTSW |
1 |
75,430,913 (GRCm38) |
missense |
probably damaging |
1.00 |
R7002:Speg
|
UTSW |
1 |
75,423,268 (GRCm38) |
missense |
probably damaging |
0.98 |
R7082:Speg
|
UTSW |
1 |
75,411,447 (GRCm38) |
missense |
probably damaging |
0.96 |
R7140:Speg
|
UTSW |
1 |
75,406,770 (GRCm38) |
critical splice donor site |
probably null |
|
R7175:Speg
|
UTSW |
1 |
75,422,490 (GRCm38) |
missense |
probably benign |
0.01 |
R7178:Speg
|
UTSW |
1 |
75,422,383 (GRCm38) |
missense |
possibly damaging |
0.46 |
R7345:Speg
|
UTSW |
1 |
75,384,835 (GRCm38) |
missense |
probably damaging |
0.97 |
R7420:Speg
|
UTSW |
1 |
75,430,905 (GRCm38) |
missense |
probably damaging |
1.00 |
R7537:Speg
|
UTSW |
1 |
75,401,464 (GRCm38) |
missense |
probably damaging |
1.00 |
R7562:Speg
|
UTSW |
1 |
75,431,279 (GRCm38) |
missense |
probably damaging |
0.97 |
R7615:Speg
|
UTSW |
1 |
75,429,242 (GRCm38) |
missense |
probably damaging |
1.00 |
R7679:Speg
|
UTSW |
1 |
75,406,315 (GRCm38) |
missense |
probably damaging |
1.00 |
R7692:Speg
|
UTSW |
1 |
75,401,190 (GRCm38) |
missense |
probably benign |
0.04 |
R7696:Speg
|
UTSW |
1 |
75,429,161 (GRCm38) |
missense |
probably damaging |
1.00 |
R7719:Speg
|
UTSW |
1 |
75,375,825 (GRCm38) |
missense |
probably damaging |
1.00 |
R7794:Speg
|
UTSW |
1 |
75,388,870 (GRCm38) |
missense |
probably benign |
0.00 |
R7824:Speg
|
UTSW |
1 |
75,384,017 (GRCm38) |
splice site |
probably null |
|
R7834:Speg
|
UTSW |
1 |
75,384,927 (GRCm38) |
missense |
probably damaging |
1.00 |
R7892:Speg
|
UTSW |
1 |
75,427,166 (GRCm38) |
missense |
probably damaging |
1.00 |
R8015:Speg
|
UTSW |
1 |
75,415,421 (GRCm38) |
splice site |
probably benign |
|
R8068:Speg
|
UTSW |
1 |
75,422,250 (GRCm38) |
missense |
probably damaging |
1.00 |
R8085:Speg
|
UTSW |
1 |
75,415,353 (GRCm38) |
missense |
probably damaging |
1.00 |
R8130:Speg
|
UTSW |
1 |
75,415,596 (GRCm38) |
missense |
probably damaging |
1.00 |
R8132:Speg
|
UTSW |
1 |
75,422,995 (GRCm38) |
missense |
probably damaging |
1.00 |
R8239:Speg
|
UTSW |
1 |
75,419,033 (GRCm38) |
missense |
probably damaging |
1.00 |
R8287:Speg
|
UTSW |
1 |
75,422,236 (GRCm38) |
missense |
probably benign |
0.26 |
R8299:Speg
|
UTSW |
1 |
75,387,836 (GRCm38) |
missense |
possibly damaging |
0.95 |
R8441:Speg
|
UTSW |
1 |
75,411,332 (GRCm38) |
missense |
possibly damaging |
0.60 |
R8468:Speg
|
UTSW |
1 |
75,431,309 (GRCm38) |
missense |
probably damaging |
1.00 |
R8555:Speg
|
UTSW |
1 |
75,402,264 (GRCm38) |
splice site |
probably null |
|
R8781:Speg
|
UTSW |
1 |
75,407,021 (GRCm38) |
missense |
probably damaging |
1.00 |
R8784:Speg
|
UTSW |
1 |
75,405,149 (GRCm38) |
critical splice donor site |
probably benign |
|
R8848:Speg
|
UTSW |
1 |
75,427,438 (GRCm38) |
critical splice donor site |
probably null |
|
R8881:Speg
|
UTSW |
1 |
75,401,151 (GRCm38) |
missense |
possibly damaging |
0.67 |
R8898:Speg
|
UTSW |
1 |
75,388,873 (GRCm38) |
missense |
probably damaging |
1.00 |
R8935:Speg
|
UTSW |
1 |
75,422,606 (GRCm38) |
missense |
probably benign |
0.30 |
R9019:Speg
|
UTSW |
1 |
75,429,238 (GRCm38) |
missense |
probably damaging |
1.00 |
R9027:Speg
|
UTSW |
1 |
75,388,432 (GRCm38) |
missense |
possibly damaging |
0.67 |
R9066:Speg
|
UTSW |
1 |
75,385,010 (GRCm38) |
missense |
probably damaging |
0.99 |
R9092:Speg
|
UTSW |
1 |
75,422,734 (GRCm38) |
missense |
probably benign |
0.01 |
R9117:Speg
|
UTSW |
1 |
75,387,800 (GRCm38) |
missense |
probably damaging |
1.00 |
R9202:Speg
|
UTSW |
1 |
75,390,993 (GRCm38) |
missense |
probably damaging |
1.00 |
R9246:Speg
|
UTSW |
1 |
75,384,854 (GRCm38) |
missense |
probably damaging |
1.00 |
R9248:Speg
|
UTSW |
1 |
75,421,776 (GRCm38) |
missense |
probably damaging |
1.00 |
R9451:Speg
|
UTSW |
1 |
75,417,733 (GRCm38) |
missense |
probably damaging |
1.00 |
R9452:Speg
|
UTSW |
1 |
75,422,508 (GRCm38) |
missense |
probably benign |
|
R9475:Speg
|
UTSW |
1 |
75,388,091 (GRCm38) |
missense |
probably damaging |
1.00 |
R9476:Speg
|
UTSW |
1 |
75,401,124 (GRCm38) |
missense |
probably damaging |
0.99 |
R9510:Speg
|
UTSW |
1 |
75,401,124 (GRCm38) |
missense |
probably damaging |
0.99 |
R9519:Speg
|
UTSW |
1 |
75,415,736 (GRCm38) |
missense |
probably damaging |
1.00 |
R9528:Speg
|
UTSW |
1 |
75,387,803 (GRCm38) |
missense |
possibly damaging |
0.78 |
R9542:Speg
|
UTSW |
1 |
75,422,782 (GRCm38) |
missense |
probably benign |
0.08 |
R9553:Speg
|
UTSW |
1 |
75,418,001 (GRCm38) |
missense |
probably benign |
0.00 |
R9767:Speg
|
UTSW |
1 |
75,427,181 (GRCm38) |
missense |
possibly damaging |
0.78 |
R9768:Speg
|
UTSW |
1 |
75,418,973 (GRCm38) |
nonsense |
probably null |
|
R9800:Speg
|
UTSW |
1 |
75,422,714 (GRCm38) |
missense |
probably benign |
0.03 |
X0025:Speg
|
UTSW |
1 |
75,422,457 (GRCm38) |
missense |
probably damaging |
1.00 |
X0026:Speg
|
UTSW |
1 |
75,423,475 (GRCm38) |
missense |
possibly damaging |
0.88 |
Z1176:Speg
|
UTSW |
1 |
75,406,594 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Speg
|
UTSW |
1 |
75,427,683 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1177:Speg
|
UTSW |
1 |
75,430,455 (GRCm38) |
missense |
probably damaging |
0.99 |
Z1177:Speg
|
UTSW |
1 |
75,428,381 (GRCm38) |
missense |
probably damaging |
1.00 |
|