Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgre1 |
C |
T |
17: 57,785,879 (GRCm39) |
T875I |
probably damaging |
Het |
Anln |
A |
T |
9: 22,293,545 (GRCm39) |
S33T |
probably benign |
Het |
Anxa6 |
T |
C |
11: 54,877,011 (GRCm39) |
T541A |
probably benign |
Het |
Atxn2 |
C |
T |
5: 121,917,557 (GRCm39) |
R334W |
probably damaging |
Het |
AU040320 |
T |
A |
4: 126,741,612 (GRCm39) |
V940D |
probably damaging |
Het |
Bcl2 |
A |
T |
1: 106,471,011 (GRCm39) |
Y232N |
probably damaging |
Het |
Bmp7 |
A |
G |
2: 172,781,855 (GRCm39) |
V3A |
probably benign |
Het |
Calr |
A |
T |
8: 85,571,557 (GRCm39) |
H145Q |
probably damaging |
Het |
Camta2 |
T |
A |
11: 70,562,792 (GRCm39) |
T976S |
probably benign |
Het |
Ccnk |
G |
A |
12: 108,168,473 (GRCm39) |
|
probably benign |
Het |
Cntln |
T |
C |
4: 85,015,029 (GRCm39) |
S1107P |
probably damaging |
Het |
Cradd |
T |
C |
10: 95,011,789 (GRCm39) |
D117G |
probably damaging |
Het |
Dcaf7 |
C |
T |
11: 105,937,647 (GRCm39) |
T90I |
probably damaging |
Het |
Defb30 |
T |
A |
14: 63,273,552 (GRCm39) |
|
probably null |
Het |
Dock4 |
T |
A |
12: 40,795,745 (GRCm39) |
I854N |
probably damaging |
Het |
Dym |
T |
A |
18: 75,189,809 (GRCm39) |
Y132* |
probably null |
Het |
Eef1a2 |
T |
C |
2: 180,791,477 (GRCm39) |
T341A |
probably benign |
Het |
Eml2 |
T |
C |
7: 18,930,206 (GRCm39) |
V309A |
probably damaging |
Het |
Flnb |
C |
T |
14: 7,905,640 (GRCm38) |
P1130L |
possibly damaging |
Het |
Hivep3 |
C |
A |
4: 119,952,085 (GRCm39) |
Q134K |
possibly damaging |
Het |
Kbtbd2 |
T |
A |
6: 56,757,011 (GRCm39) |
K242* |
probably null |
Het |
Kel |
A |
G |
6: 41,680,694 (GRCm39) |
|
probably null |
Het |
Lcorl |
T |
A |
5: 45,904,546 (GRCm39) |
K177N |
probably damaging |
Het |
Mbd3l2 |
A |
G |
9: 18,354,795 (GRCm39) |
|
probably benign |
Het |
Ms4a1 |
C |
A |
19: 11,230,542 (GRCm39) |
|
probably null |
Het |
Muc5ac |
C |
T |
7: 141,363,481 (GRCm39) |
|
probably benign |
Het |
Mylk |
C |
A |
16: 34,694,520 (GRCm39) |
P193Q |
probably benign |
Het |
Or1j11 |
T |
A |
2: 36,311,832 (GRCm39) |
C141S |
probably damaging |
Het |
Or2y16 |
G |
T |
11: 49,334,767 (GRCm39) |
A30S |
probably benign |
Het |
Or2y17 |
A |
T |
11: 49,231,580 (GRCm39) |
T74S |
probably damaging |
Het |
Or4d10b |
A |
T |
19: 12,036,777 (GRCm39) |
F113Y |
probably damaging |
Het |
Or4f52 |
C |
T |
2: 111,061,542 (GRCm39) |
V199I |
probably benign |
Het |
Otogl |
C |
T |
10: 107,663,667 (GRCm39) |
S968N |
probably damaging |
Het |
Oxr1 |
T |
G |
15: 41,686,783 (GRCm39) |
V555G |
probably damaging |
Het |
Parp12 |
T |
C |
6: 39,088,670 (GRCm39) |
I189V |
probably benign |
Het |
Peg3 |
T |
C |
7: 6,715,761 (GRCm39) |
Y103C |
probably damaging |
Het |
Plekhh2 |
T |
C |
17: 84,925,427 (GRCm39) |
V1408A |
probably benign |
Het |
Prkacb |
T |
C |
3: 146,451,133 (GRCm39) |
Y204C |
probably damaging |
Het |
Prkch |
A |
G |
12: 73,806,391 (GRCm39) |
E546G |
probably damaging |
Het |
Prss12 |
C |
A |
3: 123,241,033 (GRCm39) |
H76N |
probably benign |
Het |
Rai14 |
G |
T |
15: 10,633,254 (GRCm39) |
S45R |
possibly damaging |
Het |
Samd9l |
T |
A |
6: 3,374,750 (GRCm39) |
D837V |
probably benign |
Het |
Slc22a6 |
G |
T |
19: 8,595,805 (GRCm39) |
C49F |
probably damaging |
Het |
Slc2a2 |
T |
A |
3: 28,775,874 (GRCm39) |
I328N |
probably damaging |
Het |
Slc35f4 |
T |
C |
14: 49,556,310 (GRCm39) |
I148V |
possibly damaging |
Het |
Stk32b |
A |
T |
5: 37,606,149 (GRCm39) |
|
probably null |
Het |
Tasor |
T |
A |
14: 27,183,115 (GRCm39) |
F525I |
probably damaging |
Het |
Tktl2 |
T |
C |
8: 66,964,991 (GRCm39) |
I183T |
probably damaging |
Het |
Tmem175 |
A |
C |
5: 108,793,845 (GRCm39) |
H325P |
probably damaging |
Het |
Tns3 |
A |
G |
11: 8,443,196 (GRCm39) |
V389A |
probably damaging |
Het |
Trappc9 |
A |
T |
15: 72,809,011 (GRCm39) |
|
probably null |
Het |
Trim28 |
T |
A |
7: 12,763,385 (GRCm39) |
F509I |
possibly damaging |
Het |
Vmn1r210 |
T |
A |
13: 23,011,713 (GRCm39) |
Q191L |
probably benign |
Het |
Vmn2r24 |
A |
T |
6: 123,756,117 (GRCm39) |
D63V |
possibly damaging |
Het |
Zfp536 |
A |
G |
7: 37,267,940 (GRCm39) |
L492P |
probably damaging |
Het |
Zfp831 |
C |
A |
2: 174,488,533 (GRCm39) |
N1069K |
possibly damaging |
Het |
Zfp943 |
T |
A |
17: 22,211,593 (GRCm39) |
H226Q |
probably damaging |
Het |
|
Other mutations in Mcm3ap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Mcm3ap
|
APN |
10 |
76,307,011 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00742:Mcm3ap
|
APN |
10 |
76,328,769 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00898:Mcm3ap
|
APN |
10 |
76,306,159 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00984:Mcm3ap
|
APN |
10 |
76,335,400 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01591:Mcm3ap
|
APN |
10 |
76,306,639 (GRCm39) |
missense |
probably benign |
|
IGL01882:Mcm3ap
|
APN |
10 |
76,319,018 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01973:Mcm3ap
|
APN |
10 |
76,306,951 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02253:Mcm3ap
|
APN |
10 |
76,305,899 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02304:Mcm3ap
|
APN |
10 |
76,320,572 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02340:Mcm3ap
|
APN |
10 |
76,332,386 (GRCm39) |
nonsense |
probably null |
|
IGL02487:Mcm3ap
|
APN |
10 |
76,343,389 (GRCm39) |
unclassified |
probably benign |
|
IGL02488:Mcm3ap
|
APN |
10 |
76,335,483 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02640:Mcm3ap
|
APN |
10 |
76,342,255 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02714:Mcm3ap
|
APN |
10 |
76,346,867 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02748:Mcm3ap
|
APN |
10 |
76,337,082 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02894:Mcm3ap
|
APN |
10 |
76,313,601 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02903:Mcm3ap
|
APN |
10 |
76,307,092 (GRCm39) |
splice site |
probably benign |
|
IGL02955:Mcm3ap
|
APN |
10 |
76,343,300 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02989:Mcm3ap
|
APN |
10 |
76,306,894 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL03003:Mcm3ap
|
APN |
10 |
76,340,531 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03081:Mcm3ap
|
APN |
10 |
76,306,150 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03218:Mcm3ap
|
APN |
10 |
76,318,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03401:Mcm3ap
|
APN |
10 |
76,320,483 (GRCm39) |
splice site |
probably benign |
|
Bane
|
UTSW |
10 |
76,319,060 (GRCm39) |
missense |
probably damaging |
1.00 |
Doom
|
UTSW |
10 |
76,337,148 (GRCm39) |
missense |
probably benign |
|
woeful
|
UTSW |
10 |
76,316,849 (GRCm39) |
missense |
probably benign |
0.44 |
PIT4377001:Mcm3ap
|
UTSW |
10 |
76,338,596 (GRCm39) |
missense |
possibly damaging |
0.78 |
PIT4791001:Mcm3ap
|
UTSW |
10 |
76,342,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R0105:Mcm3ap
|
UTSW |
10 |
76,335,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R0144:Mcm3ap
|
UTSW |
10 |
76,316,849 (GRCm39) |
missense |
probably benign |
0.44 |
R0423:Mcm3ap
|
UTSW |
10 |
76,338,539 (GRCm39) |
missense |
probably benign |
0.00 |
R0692:Mcm3ap
|
UTSW |
10 |
76,319,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R1402:Mcm3ap
|
UTSW |
10 |
76,313,748 (GRCm39) |
unclassified |
probably benign |
|
R1441:Mcm3ap
|
UTSW |
10 |
76,307,000 (GRCm39) |
missense |
probably benign |
|
R1512:Mcm3ap
|
UTSW |
10 |
76,306,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R1533:Mcm3ap
|
UTSW |
10 |
76,340,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R1569:Mcm3ap
|
UTSW |
10 |
76,319,022 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1590:Mcm3ap
|
UTSW |
10 |
76,332,375 (GRCm39) |
missense |
probably benign |
0.36 |
R1597:Mcm3ap
|
UTSW |
10 |
76,319,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R1743:Mcm3ap
|
UTSW |
10 |
76,320,508 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1773:Mcm3ap
|
UTSW |
10 |
76,306,994 (GRCm39) |
missense |
probably benign |
|
R1922:Mcm3ap
|
UTSW |
10 |
76,343,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Mcm3ap
|
UTSW |
10 |
76,305,902 (GRCm39) |
missense |
probably benign |
0.43 |
R2097:Mcm3ap
|
UTSW |
10 |
76,348,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R2436:Mcm3ap
|
UTSW |
10 |
76,325,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R3684:Mcm3ap
|
UTSW |
10 |
76,325,260 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3690:Mcm3ap
|
UTSW |
10 |
76,318,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R3881:Mcm3ap
|
UTSW |
10 |
76,342,280 (GRCm39) |
missense |
probably benign |
0.21 |
R4296:Mcm3ap
|
UTSW |
10 |
76,343,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R4677:Mcm3ap
|
UTSW |
10 |
76,306,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R4786:Mcm3ap
|
UTSW |
10 |
76,324,300 (GRCm39) |
missense |
probably benign |
0.00 |
R4882:Mcm3ap
|
UTSW |
10 |
76,320,495 (GRCm39) |
nonsense |
probably null |
|
R4907:Mcm3ap
|
UTSW |
10 |
76,329,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R5108:Mcm3ap
|
UTSW |
10 |
76,338,536 (GRCm39) |
missense |
probably benign |
0.04 |
R5279:Mcm3ap
|
UTSW |
10 |
76,343,373 (GRCm39) |
missense |
probably damaging |
0.96 |
R5316:Mcm3ap
|
UTSW |
10 |
76,306,760 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5402:Mcm3ap
|
UTSW |
10 |
76,319,148 (GRCm39) |
missense |
probably benign |
0.04 |
R5459:Mcm3ap
|
UTSW |
10 |
76,332,316 (GRCm39) |
nonsense |
probably null |
|
R5473:Mcm3ap
|
UTSW |
10 |
76,338,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R5570:Mcm3ap
|
UTSW |
10 |
76,316,930 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5931:Mcm3ap
|
UTSW |
10 |
76,307,000 (GRCm39) |
missense |
probably benign |
|
R5939:Mcm3ap
|
UTSW |
10 |
76,344,195 (GRCm39) |
missense |
probably benign |
0.00 |
R5950:Mcm3ap
|
UTSW |
10 |
76,324,253 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5998:Mcm3ap
|
UTSW |
10 |
76,316,976 (GRCm39) |
critical splice donor site |
probably null |
|
R6122:Mcm3ap
|
UTSW |
10 |
76,342,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R6192:Mcm3ap
|
UTSW |
10 |
76,336,934 (GRCm39) |
missense |
probably damaging |
0.97 |
R6226:Mcm3ap
|
UTSW |
10 |
76,351,540 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6293:Mcm3ap
|
UTSW |
10 |
76,307,312 (GRCm39) |
nonsense |
probably null |
|
R6669:Mcm3ap
|
UTSW |
10 |
76,343,171 (GRCm39) |
missense |
probably damaging |
0.98 |
R6715:Mcm3ap
|
UTSW |
10 |
76,325,366 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6759:Mcm3ap
|
UTSW |
10 |
76,337,148 (GRCm39) |
missense |
probably benign |
|
R6870:Mcm3ap
|
UTSW |
10 |
76,306,049 (GRCm39) |
missense |
probably benign |
0.00 |
R6935:Mcm3ap
|
UTSW |
10 |
76,340,087 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6947:Mcm3ap
|
UTSW |
10 |
76,351,500 (GRCm39) |
missense |
probably benign |
0.09 |
R7212:Mcm3ap
|
UTSW |
10 |
76,337,145 (GRCm39) |
missense |
probably benign |
0.01 |
R7403:Mcm3ap
|
UTSW |
10 |
76,318,657 (GRCm39) |
critical splice donor site |
probably null |
|
R7470:Mcm3ap
|
UTSW |
10 |
76,344,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R7561:Mcm3ap
|
UTSW |
10 |
76,328,712 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7610:Mcm3ap
|
UTSW |
10 |
76,332,554 (GRCm39) |
splice site |
probably null |
|
R7620:Mcm3ap
|
UTSW |
10 |
76,306,267 (GRCm39) |
missense |
probably benign |
0.00 |
R7898:Mcm3ap
|
UTSW |
10 |
76,342,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R8266:Mcm3ap
|
UTSW |
10 |
76,312,414 (GRCm39) |
nonsense |
probably null |
|
R8355:Mcm3ap
|
UTSW |
10 |
76,329,335 (GRCm39) |
missense |
probably benign |
0.32 |
R8367:Mcm3ap
|
UTSW |
10 |
76,313,693 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8867:Mcm3ap
|
UTSW |
10 |
76,306,538 (GRCm39) |
missense |
probably benign |
0.31 |
R9282:Mcm3ap
|
UTSW |
10 |
76,342,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R9319:Mcm3ap
|
UTSW |
10 |
76,318,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R9339:Mcm3ap
|
UTSW |
10 |
76,306,358 (GRCm39) |
missense |
probably benign |
0.04 |
R9554:Mcm3ap
|
UTSW |
10 |
76,332,310 (GRCm39) |
missense |
probably damaging |
0.97 |
R9706:Mcm3ap
|
UTSW |
10 |
76,312,352 (GRCm39) |
missense |
probably damaging |
1.00 |
X0026:Mcm3ap
|
UTSW |
10 |
76,318,619 (GRCm39) |
nonsense |
probably null |
|
|