Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm5 |
T |
C |
4: 144,504,332 (GRCm39) |
D273G |
probably damaging |
Het |
Acacb |
T |
C |
5: 114,333,703 (GRCm39) |
V542A |
possibly damaging |
Het |
Adprhl1 |
C |
T |
8: 13,273,069 (GRCm39) |
V1230I |
probably benign |
Het |
Agpat1 |
T |
A |
17: 34,829,883 (GRCm39) |
Y77N |
probably damaging |
Het |
Apc |
T |
A |
18: 34,445,126 (GRCm39) |
I674K |
probably damaging |
Het |
Arpc5 |
T |
C |
1: 152,647,187 (GRCm39) |
S97P |
probably damaging |
Het |
Arrdc5 |
A |
G |
17: 56,604,931 (GRCm39) |
F119L |
probably benign |
Het |
Asap1 |
A |
G |
15: 64,002,105 (GRCm39) |
V402A |
probably damaging |
Het |
Aspg |
T |
C |
12: 112,091,255 (GRCm39) |
V479A |
possibly damaging |
Het |
B3galnt2 |
G |
A |
13: 14,169,070 (GRCm39) |
V368M |
probably benign |
Het |
Bcl3 |
T |
C |
7: 19,556,536 (GRCm39) |
T23A |
probably benign |
Het |
Bpifb5 |
A |
G |
2: 154,070,853 (GRCm39) |
K215E |
possibly damaging |
Het |
Coa4 |
T |
A |
7: 100,188,478 (GRCm39) |
C64S |
probably damaging |
Het |
Dcun1d4 |
T |
C |
5: 73,648,879 (GRCm39) |
|
probably null |
Het |
Dnaaf5 |
T |
G |
5: 139,151,868 (GRCm39) |
C506W |
probably damaging |
Het |
Dock3 |
A |
G |
9: 106,900,931 (GRCm39) |
Y345H |
probably damaging |
Het |
Dscaml1 |
A |
G |
9: 45,621,624 (GRCm39) |
N1024S |
possibly damaging |
Het |
Dsp |
T |
C |
13: 38,360,478 (GRCm39) |
|
probably null |
Het |
Dsp |
A |
G |
13: 38,379,425 (GRCm39) |
T2057A |
probably benign |
Het |
Dync1h1 |
T |
G |
12: 110,602,887 (GRCm39) |
L2176R |
probably damaging |
Het |
Eif5b |
A |
C |
1: 38,090,718 (GRCm39) |
D1192A |
probably benign |
Het |
Epn2 |
A |
T |
11: 61,437,674 (GRCm39) |
|
probably benign |
Het |
Exoc1 |
T |
A |
5: 76,693,195 (GRCm39) |
N360K |
probably benign |
Het |
Fam135b |
A |
T |
15: 71,335,529 (GRCm39) |
V555E |
probably damaging |
Het |
Fmn1 |
A |
T |
2: 113,271,956 (GRCm39) |
Q108L |
unknown |
Het |
Gcc2 |
A |
G |
10: 58,092,723 (GRCm39) |
T48A |
probably benign |
Het |
Gm6619 |
T |
G |
6: 131,467,354 (GRCm39) |
I73S |
possibly damaging |
Het |
Gm8267 |
T |
A |
14: 44,960,397 (GRCm39) |
D116V |
probably damaging |
Het |
Hapln3 |
T |
A |
7: 78,767,017 (GRCm39) |
T341S |
probably benign |
Het |
Lamb3 |
C |
A |
1: 193,014,474 (GRCm39) |
D544E |
possibly damaging |
Het |
Lhx5 |
T |
A |
5: 120,578,349 (GRCm39) |
S390T |
probably benign |
Het |
Lrrc63 |
A |
G |
14: 75,363,697 (GRCm39) |
S145P |
possibly damaging |
Het |
Lrriq1 |
T |
C |
10: 103,050,380 (GRCm39) |
M791V |
probably benign |
Het |
Lyg2 |
A |
G |
1: 37,950,218 (GRCm39) |
Y37H |
possibly damaging |
Het |
Lyz3 |
G |
A |
10: 117,074,602 (GRCm39) |
|
probably benign |
Het |
Nrbp1 |
T |
A |
5: 31,402,300 (GRCm39) |
M172K |
probably damaging |
Het |
Or2l13b |
T |
G |
16: 19,349,650 (GRCm39) |
S7R |
probably benign |
Het |
Or4c126 |
A |
G |
2: 89,824,183 (GRCm39) |
I149V |
probably benign |
Het |
Or8u9 |
T |
A |
2: 86,001,354 (GRCm39) |
D269V |
probably damaging |
Het |
Pcyt2 |
A |
T |
11: 120,502,209 (GRCm39) |
Y308N |
possibly damaging |
Het |
Peg10 |
C |
CTCA |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Phf21b |
A |
G |
15: 84,689,104 (GRCm39) |
S141P |
probably damaging |
Het |
Pigh |
G |
A |
12: 79,136,324 (GRCm39) |
P24S |
probably benign |
Het |
Plekhg3 |
A |
G |
12: 76,623,259 (GRCm39) |
D834G |
probably damaging |
Het |
Plekhg5 |
T |
A |
4: 152,198,392 (GRCm39) |
V860D |
probably benign |
Het |
Pon1 |
A |
G |
6: 5,177,399 (GRCm39) |
I170T |
probably damaging |
Het |
Ptpn9 |
T |
A |
9: 56,934,717 (GRCm39) |
Y160* |
probably null |
Het |
Ptprj |
T |
C |
2: 90,280,163 (GRCm39) |
K1045R |
possibly damaging |
Het |
Rilpl2 |
T |
A |
5: 124,601,851 (GRCm39) |
H196L |
probably benign |
Het |
Rnf112 |
C |
T |
11: 61,341,854 (GRCm39) |
V317I |
possibly damaging |
Het |
Rundc3a |
G |
T |
11: 102,290,872 (GRCm39) |
|
probably null |
Het |
Sgsm1 |
T |
C |
5: 113,422,187 (GRCm39) |
Y489C |
probably damaging |
Het |
Slc26a9 |
A |
G |
1: 131,690,556 (GRCm39) |
Y520C |
probably damaging |
Het |
Smc5 |
A |
G |
19: 23,220,064 (GRCm39) |
V467A |
probably damaging |
Het |
Spata20 |
G |
A |
11: 94,374,867 (GRCm39) |
A245V |
probably benign |
Het |
Steap3 |
A |
C |
1: 120,169,248 (GRCm39) |
F350V |
probably benign |
Het |
Sucnr1 |
A |
G |
3: 59,994,117 (GRCm39) |
Q215R |
probably benign |
Het |
Supv3l1 |
G |
A |
10: 62,266,394 (GRCm39) |
A594V |
probably damaging |
Het |
Swt1 |
A |
T |
1: 151,286,815 (GRCm39) |
F226I |
probably benign |
Het |
Taar7f |
A |
G |
10: 23,925,885 (GRCm39) |
T160A |
possibly damaging |
Het |
Tada2a |
A |
T |
11: 84,017,812 (GRCm39) |
|
probably null |
Het |
Taok3 |
C |
A |
5: 117,388,974 (GRCm39) |
Q460K |
probably damaging |
Het |
Tasor |
T |
A |
14: 27,193,602 (GRCm39) |
V934E |
probably damaging |
Het |
Twf2 |
A |
G |
9: 106,091,597 (GRCm39) |
E268G |
probably damaging |
Het |
Upf2 |
A |
T |
2: 6,023,743 (GRCm39) |
I698F |
unknown |
Het |
Vmn2r35 |
T |
A |
7: 7,820,013 (GRCm39) |
N86Y |
probably damaging |
Het |
Vmn2r84 |
T |
C |
10: 130,227,982 (GRCm39) |
T85A |
possibly damaging |
Het |
Vps13d |
A |
G |
4: 144,832,426 (GRCm39) |
S2833P |
|
Het |
Xrn1 |
T |
C |
9: 95,933,682 (GRCm39) |
S1584P |
probably benign |
Het |
Zfp354b |
T |
C |
11: 50,813,224 (GRCm39) |
Y567C |
probably damaging |
Het |
Zfp52 |
A |
T |
17: 21,781,132 (GRCm39) |
R327* |
probably null |
Het |
|
Other mutations in Sis |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00582:Sis
|
APN |
3 |
72,853,969 (GRCm39) |
missense |
probably benign |
|
IGL00715:Sis
|
APN |
3 |
72,841,457 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00721:Sis
|
APN |
3 |
72,850,912 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00766:Sis
|
APN |
3 |
72,814,570 (GRCm39) |
splice site |
probably benign |
|
IGL00783:Sis
|
APN |
3 |
72,853,965 (GRCm39) |
missense |
probably benign |
|
IGL00805:Sis
|
APN |
3 |
72,841,532 (GRCm39) |
missense |
probably benign |
0.05 |
IGL00932:Sis
|
APN |
3 |
72,848,289 (GRCm39) |
splice site |
probably benign |
|
IGL01020:Sis
|
APN |
3 |
72,874,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01024:Sis
|
APN |
3 |
72,819,209 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01286:Sis
|
APN |
3 |
72,848,358 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01457:Sis
|
APN |
3 |
72,868,354 (GRCm39) |
missense |
probably benign |
|
IGL01514:Sis
|
APN |
3 |
72,843,253 (GRCm39) |
splice site |
probably benign |
|
IGL01986:Sis
|
APN |
3 |
72,852,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02110:Sis
|
APN |
3 |
72,836,032 (GRCm39) |
nonsense |
probably null |
|
IGL02132:Sis
|
APN |
3 |
72,854,804 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02152:Sis
|
APN |
3 |
72,796,319 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02200:Sis
|
APN |
3 |
72,850,937 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02244:Sis
|
APN |
3 |
72,863,523 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02307:Sis
|
APN |
3 |
72,819,167 (GRCm39) |
splice site |
probably benign |
|
IGL02374:Sis
|
APN |
3 |
72,832,789 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02437:Sis
|
APN |
3 |
72,826,947 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02571:Sis
|
APN |
3 |
72,863,637 (GRCm39) |
splice site |
probably benign |
|
IGL02601:Sis
|
APN |
3 |
72,820,543 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03063:Sis
|
APN |
3 |
72,835,630 (GRCm39) |
missense |
probably benign |
|
IGL03382:Sis
|
APN |
3 |
72,836,052 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03397:Sis
|
APN |
3 |
72,843,212 (GRCm39) |
missense |
probably benign |
0.44 |
PIT1430001:Sis
|
UTSW |
3 |
72,830,162 (GRCm39) |
missense |
probably damaging |
0.97 |
R0013:Sis
|
UTSW |
3 |
72,817,809 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0013:Sis
|
UTSW |
3 |
72,817,809 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0046:Sis
|
UTSW |
3 |
72,839,427 (GRCm39) |
missense |
probably benign |
0.01 |
R0094:Sis
|
UTSW |
3 |
72,828,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R0096:Sis
|
UTSW |
3 |
72,835,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R0505:Sis
|
UTSW |
3 |
72,867,629 (GRCm39) |
missense |
probably benign |
0.29 |
R0544:Sis
|
UTSW |
3 |
72,858,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R0551:Sis
|
UTSW |
3 |
72,832,740 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0617:Sis
|
UTSW |
3 |
72,872,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R0698:Sis
|
UTSW |
3 |
72,817,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0701:Sis
|
UTSW |
3 |
72,848,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R0704:Sis
|
UTSW |
3 |
72,857,155 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0706:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0710:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0752:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0753:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0754:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0767:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0769:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0772:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0774:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0776:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0818:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0819:Sis
|
UTSW |
3 |
72,859,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R0885:Sis
|
UTSW |
3 |
72,819,282 (GRCm39) |
nonsense |
probably null |
|
R1076:Sis
|
UTSW |
3 |
72,841,431 (GRCm39) |
missense |
probably damaging |
0.97 |
R1140:Sis
|
UTSW |
3 |
72,858,949 (GRCm39) |
missense |
probably damaging |
0.98 |
R1175:Sis
|
UTSW |
3 |
72,865,437 (GRCm39) |
splice site |
probably benign |
|
R1301:Sis
|
UTSW |
3 |
72,853,915 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1437:Sis
|
UTSW |
3 |
72,841,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Sis
|
UTSW |
3 |
72,839,393 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1466:Sis
|
UTSW |
3 |
72,839,393 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1472:Sis
|
UTSW |
3 |
72,796,360 (GRCm39) |
missense |
probably benign |
0.12 |
R1584:Sis
|
UTSW |
3 |
72,839,393 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1707:Sis
|
UTSW |
3 |
72,816,420 (GRCm39) |
splice site |
probably benign |
|
R1715:Sis
|
UTSW |
3 |
72,796,343 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1719:Sis
|
UTSW |
3 |
72,872,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R1728:Sis
|
UTSW |
3 |
72,872,978 (GRCm39) |
nonsense |
probably null |
|
R1784:Sis
|
UTSW |
3 |
72,872,978 (GRCm39) |
nonsense |
probably null |
|
R1820:Sis
|
UTSW |
3 |
72,828,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R1972:Sis
|
UTSW |
3 |
72,828,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R1973:Sis
|
UTSW |
3 |
72,828,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R2054:Sis
|
UTSW |
3 |
72,820,570 (GRCm39) |
missense |
probably benign |
0.01 |
R2233:Sis
|
UTSW |
3 |
72,820,527 (GRCm39) |
missense |
probably benign |
0.03 |
R2235:Sis
|
UTSW |
3 |
72,820,527 (GRCm39) |
missense |
probably benign |
0.03 |
R2276:Sis
|
UTSW |
3 |
72,821,934 (GRCm39) |
nonsense |
probably null |
|
R2435:Sis
|
UTSW |
3 |
72,819,237 (GRCm39) |
missense |
probably benign |
0.01 |
R2885:Sis
|
UTSW |
3 |
72,816,506 (GRCm39) |
missense |
probably benign |
0.01 |
R2966:Sis
|
UTSW |
3 |
72,796,343 (GRCm39) |
missense |
probably benign |
0.30 |
R3708:Sis
|
UTSW |
3 |
72,850,856 (GRCm39) |
missense |
probably benign |
0.02 |
R3790:Sis
|
UTSW |
3 |
72,828,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R3807:Sis
|
UTSW |
3 |
72,832,929 (GRCm39) |
missense |
probably benign |
0.01 |
R3858:Sis
|
UTSW |
3 |
72,835,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R3974:Sis
|
UTSW |
3 |
72,850,968 (GRCm39) |
missense |
probably damaging |
0.96 |
R3975:Sis
|
UTSW |
3 |
72,850,968 (GRCm39) |
missense |
probably damaging |
0.96 |
R4037:Sis
|
UTSW |
3 |
72,835,935 (GRCm39) |
missense |
probably benign |
|
R4080:Sis
|
UTSW |
3 |
72,828,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R4204:Sis
|
UTSW |
3 |
72,868,415 (GRCm39) |
missense |
probably benign |
|
R4394:Sis
|
UTSW |
3 |
72,863,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R4470:Sis
|
UTSW |
3 |
72,835,492 (GRCm39) |
splice site |
probably null |
|
R4573:Sis
|
UTSW |
3 |
72,835,570 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4868:Sis
|
UTSW |
3 |
72,850,881 (GRCm39) |
missense |
probably benign |
0.09 |
R5023:Sis
|
UTSW |
3 |
72,841,455 (GRCm39) |
missense |
probably benign |
0.05 |
R5264:Sis
|
UTSW |
3 |
72,857,089 (GRCm39) |
missense |
probably damaging |
0.98 |
R5414:Sis
|
UTSW |
3 |
72,859,826 (GRCm39) |
missense |
probably benign |
|
R5462:Sis
|
UTSW |
3 |
72,857,171 (GRCm39) |
missense |
probably damaging |
0.96 |
R5523:Sis
|
UTSW |
3 |
72,798,754 (GRCm39) |
missense |
probably benign |
0.00 |
R5584:Sis
|
UTSW |
3 |
72,817,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R5587:Sis
|
UTSW |
3 |
72,821,909 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5725:Sis
|
UTSW |
3 |
72,872,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R5769:Sis
|
UTSW |
3 |
72,835,568 (GRCm39) |
missense |
probably damaging |
0.98 |
R5790:Sis
|
UTSW |
3 |
72,835,507 (GRCm39) |
missense |
probably benign |
|
R5864:Sis
|
UTSW |
3 |
72,857,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R5902:Sis
|
UTSW |
3 |
72,867,589 (GRCm39) |
critical splice donor site |
probably null |
|
R5925:Sis
|
UTSW |
3 |
72,828,713 (GRCm39) |
splice site |
probably null |
|
R6018:Sis
|
UTSW |
3 |
72,820,525 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6029:Sis
|
UTSW |
3 |
72,835,641 (GRCm39) |
missense |
probably benign |
0.30 |
R6124:Sis
|
UTSW |
3 |
72,860,544 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6171:Sis
|
UTSW |
3 |
72,868,360 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6182:Sis
|
UTSW |
3 |
72,811,626 (GRCm39) |
missense |
probably benign |
0.05 |
R6295:Sis
|
UTSW |
3 |
72,874,103 (GRCm39) |
missense |
probably damaging |
0.99 |
R6416:Sis
|
UTSW |
3 |
72,819,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R6431:Sis
|
UTSW |
3 |
72,865,507 (GRCm39) |
missense |
probably benign |
0.00 |
R6472:Sis
|
UTSW |
3 |
72,846,067 (GRCm39) |
nonsense |
probably null |
|
R6517:Sis
|
UTSW |
3 |
72,814,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R6701:Sis
|
UTSW |
3 |
72,856,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R6796:Sis
|
UTSW |
3 |
72,872,951 (GRCm39) |
missense |
probably benign |
0.06 |
R6853:Sis
|
UTSW |
3 |
72,798,759 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6906:Sis
|
UTSW |
3 |
72,826,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R7058:Sis
|
UTSW |
3 |
72,810,940 (GRCm39) |
missense |
probably damaging |
0.98 |
R7357:Sis
|
UTSW |
3 |
72,832,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R7381:Sis
|
UTSW |
3 |
72,820,625 (GRCm39) |
splice site |
probably null |
|
R7742:Sis
|
UTSW |
3 |
72,832,431 (GRCm39) |
missense |
probably benign |
0.19 |
R7813:Sis
|
UTSW |
3 |
72,832,801 (GRCm39) |
missense |
probably benign |
0.01 |
R7883:Sis
|
UTSW |
3 |
72,828,329 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7899:Sis
|
UTSW |
3 |
72,844,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R7915:Sis
|
UTSW |
3 |
72,828,471 (GRCm39) |
missense |
probably damaging |
0.99 |
R7985:Sis
|
UTSW |
3 |
72,844,294 (GRCm39) |
splice site |
probably null |
|
R8020:Sis
|
UTSW |
3 |
72,816,298 (GRCm39) |
critical splice donor site |
probably null |
|
R8023:Sis
|
UTSW |
3 |
72,859,813 (GRCm39) |
missense |
probably damaging |
0.97 |
R8029:Sis
|
UTSW |
3 |
72,828,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R8053:Sis
|
UTSW |
3 |
72,856,901 (GRCm39) |
nonsense |
probably null |
|
R8062:Sis
|
UTSW |
3 |
72,828,321 (GRCm39) |
nonsense |
probably null |
|
R8074:Sis
|
UTSW |
3 |
72,824,531 (GRCm39) |
missense |
probably damaging |
1.00 |
R8085:Sis
|
UTSW |
3 |
72,814,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R8137:Sis
|
UTSW |
3 |
72,796,378 (GRCm39) |
missense |
probably benign |
0.22 |
R8349:Sis
|
UTSW |
3 |
72,810,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R8354:Sis
|
UTSW |
3 |
72,854,834 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8366:Sis
|
UTSW |
3 |
72,865,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R8449:Sis
|
UTSW |
3 |
72,810,984 (GRCm39) |
missense |
probably damaging |
1.00 |
R8454:Sis
|
UTSW |
3 |
72,854,834 (GRCm39) |
missense |
possibly damaging |
0.84 |
R8474:Sis
|
UTSW |
3 |
72,836,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R8515:Sis
|
UTSW |
3 |
72,836,742 (GRCm39) |
missense |
probably benign |
0.00 |
R8680:Sis
|
UTSW |
3 |
72,867,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R8703:Sis
|
UTSW |
3 |
72,867,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R9098:Sis
|
UTSW |
3 |
72,844,578 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9466:Sis
|
UTSW |
3 |
72,872,910 (GRCm39) |
critical splice donor site |
probably null |
|
R9574:Sis
|
UTSW |
3 |
72,828,490 (GRCm39) |
missense |
probably benign |
0.05 |
R9630:Sis
|
UTSW |
3 |
72,828,722 (GRCm39) |
missense |
probably benign |
0.11 |
R9680:Sis
|
UTSW |
3 |
72,863,621 (GRCm39) |
missense |
probably benign |
0.12 |
R9709:Sis
|
UTSW |
3 |
72,799,074 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9731:Sis
|
UTSW |
3 |
72,835,543 (GRCm39) |
missense |
probably benign |
0.01 |
X0009:Sis
|
UTSW |
3 |
72,796,355 (GRCm39) |
missense |
probably damaging |
0.99 |
X0024:Sis
|
UTSW |
3 |
72,836,003 (GRCm39) |
missense |
probably benign |
|
X0060:Sis
|
UTSW |
3 |
72,828,239 (GRCm39) |
intron |
probably benign |
|
Z1176:Sis
|
UTSW |
3 |
72,850,890 (GRCm39) |
missense |
probably benign |
0.25 |
Z1176:Sis
|
UTSW |
3 |
72,811,606 (GRCm39) |
missense |
probably benign |
0.05 |
Z1177:Sis
|
UTSW |
3 |
72,850,902 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sis
|
UTSW |
3 |
72,817,807 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sis
|
UTSW |
3 |
72,816,505 (GRCm39) |
missense |
possibly damaging |
0.88 |
|