Other mutations in this stock |
Total: 118 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm1 |
A |
G |
3: 59,843,771 (GRCm39) |
H155R |
possibly damaging |
Het |
Abca13 |
G |
T |
11: 9,244,559 (GRCm39) |
V2141L |
probably benign |
Het |
Adam17 |
T |
C |
12: 21,390,459 (GRCm39) |
|
probably benign |
Het |
Adam3 |
A |
T |
8: 25,185,331 (GRCm39) |
C456S |
probably damaging |
Het |
Aldh4a1 |
G |
T |
4: 139,369,882 (GRCm39) |
|
probably benign |
Het |
Anapc4 |
A |
G |
5: 52,999,359 (GRCm39) |
|
probably benign |
Het |
Ank3 |
A |
T |
10: 69,718,198 (GRCm39) |
Q483L |
probably damaging |
Het |
Ankle2 |
A |
G |
5: 110,389,925 (GRCm39) |
|
probably benign |
Het |
Ankrd13b |
T |
A |
11: 77,364,114 (GRCm39) |
T150S |
possibly damaging |
Het |
Apeh |
A |
G |
9: 107,964,254 (GRCm39) |
M524T |
probably benign |
Het |
Arl14epl |
T |
A |
18: 47,059,484 (GRCm39) |
|
probably null |
Het |
Atg2a |
T |
C |
19: 6,302,569 (GRCm39) |
F964S |
possibly damaging |
Het |
Atg2b |
C |
T |
12: 105,583,412 (GRCm39) |
V2050M |
probably damaging |
Het |
Atp2b4 |
A |
T |
1: 133,659,956 (GRCm39) |
|
probably benign |
Het |
Bbof1 |
T |
A |
12: 84,477,045 (GRCm39) |
S512T |
probably benign |
Het |
Camta1 |
C |
A |
4: 151,159,597 (GRCm39) |
R1614L |
probably damaging |
Het |
Car10 |
T |
C |
11: 93,381,408 (GRCm39) |
Y100H |
probably damaging |
Het |
Ccdc81 |
T |
A |
7: 89,542,504 (GRCm39) |
E124V |
probably damaging |
Het |
Cd84 |
A |
G |
1: 171,700,494 (GRCm39) |
T204A |
probably benign |
Het |
Celf2 |
A |
G |
2: 6,608,987 (GRCm39) |
S178P |
probably damaging |
Het |
Chat |
G |
A |
14: 32,130,976 (GRCm39) |
T555M |
probably damaging |
Het |
Chd6 |
A |
G |
2: 160,834,111 (GRCm39) |
F917S |
probably damaging |
Het |
Chrna2 |
C |
A |
14: 66,386,553 (GRCm39) |
T233N |
probably damaging |
Het |
Cnpy2 |
T |
C |
10: 128,162,054 (GRCm39) |
V109A |
probably benign |
Het |
Col4a1 |
T |
C |
8: 11,258,333 (GRCm39) |
|
probably null |
Het |
Csmd1 |
C |
T |
8: 15,982,529 (GRCm39) |
V2713M |
possibly damaging |
Het |
Cuedc1 |
G |
A |
11: 88,074,231 (GRCm39) |
R255Q |
probably damaging |
Het |
Cxcl15 |
A |
T |
5: 90,945,897 (GRCm39) |
|
probably benign |
Het |
Dach1 |
A |
T |
14: 98,138,765 (GRCm39) |
H559Q |
possibly damaging |
Het |
Dele1 |
T |
C |
18: 38,387,124 (GRCm39) |
|
probably null |
Het |
Dennd4c |
C |
T |
4: 86,744,259 (GRCm39) |
T1367M |
probably damaging |
Het |
Depdc5 |
T |
A |
5: 33,102,372 (GRCm39) |
Y365* |
probably null |
Het |
Dicer1 |
T |
C |
12: 104,669,100 (GRCm39) |
Y1194C |
possibly damaging |
Het |
Dmxl1 |
C |
G |
18: 50,024,534 (GRCm39) |
S1736* |
probably null |
Het |
Dnah7a |
C |
T |
1: 53,536,285 (GRCm39) |
R2586K |
probably benign |
Het |
Dnajb8 |
T |
C |
6: 88,199,467 (GRCm39) |
M1T |
probably null |
Het |
Dync2h1 |
G |
A |
9: 7,122,692 (GRCm39) |
P2088L |
probably benign |
Het |
Eftud2 |
T |
G |
11: 102,735,048 (GRCm39) |
H617P |
probably damaging |
Het |
Ephb1 |
A |
G |
9: 101,873,179 (GRCm39) |
|
probably benign |
Het |
Fam184a |
G |
T |
10: 53,574,975 (GRCm39) |
H155Q |
probably benign |
Het |
Firrm |
T |
C |
1: 163,799,412 (GRCm39) |
|
probably null |
Het |
Ganc |
G |
T |
2: 120,278,882 (GRCm39) |
E700* |
probably null |
Het |
Gm10912 |
A |
G |
2: 103,897,290 (GRCm39) |
|
probably benign |
Het |
Haus5 |
A |
T |
7: 30,358,492 (GRCm39) |
I294N |
probably damaging |
Het |
Hmgcr |
G |
T |
13: 96,796,651 (GRCm39) |
|
probably null |
Het |
Hr |
T |
A |
14: 70,799,352 (GRCm39) |
C641* |
probably null |
Het |
Itga10 |
A |
G |
3: 96,565,490 (GRCm39) |
N1038S |
probably damaging |
Het |
Itgb1bp1 |
T |
G |
12: 21,321,436 (GRCm39) |
Y172S |
probably damaging |
Het |
Kprp |
T |
C |
3: 92,732,030 (GRCm39) |
N340S |
probably damaging |
Het |
Kremen1 |
A |
G |
11: 5,165,447 (GRCm39) |
I41T |
probably damaging |
Het |
Krt6b |
A |
G |
15: 101,586,042 (GRCm39) |
|
probably benign |
Het |
Krt81 |
C |
A |
15: 101,361,508 (GRCm39) |
R24L |
possibly damaging |
Het |
Ldhd |
A |
G |
8: 112,356,309 (GRCm39) |
Y86H |
probably benign |
Het |
Lilra6 |
A |
T |
7: 3,915,784 (GRCm39) |
I76N |
possibly damaging |
Het |
Mak |
T |
C |
13: 41,199,743 (GRCm39) |
T299A |
probably benign |
Het |
Med25 |
A |
G |
7: 44,534,502 (GRCm39) |
|
probably null |
Het |
Mpg |
A |
T |
11: 32,180,039 (GRCm39) |
N189I |
probably damaging |
Het |
Mroh8 |
A |
G |
2: 157,071,838 (GRCm39) |
Y556H |
probably damaging |
Het |
Myh8 |
T |
A |
11: 67,175,333 (GRCm39) |
S294T |
probably benign |
Het |
Myom1 |
T |
A |
17: 71,391,312 (GRCm39) |
D842E |
probably benign |
Het |
Myorg |
A |
G |
4: 41,498,538 (GRCm39) |
F364S |
probably damaging |
Het |
Nat2 |
C |
T |
8: 67,953,982 (GRCm39) |
Q31* |
probably null |
Het |
Nf1 |
T |
A |
11: 79,329,595 (GRCm39) |
M653K |
probably benign |
Het |
Nhs |
C |
A |
X: 160,620,355 (GRCm39) |
R1467I |
probably damaging |
Het |
Npr2 |
A |
G |
4: 43,632,801 (GRCm39) |
E206G |
probably benign |
Het |
Nsd3 |
G |
A |
8: 26,168,732 (GRCm39) |
G629D |
possibly damaging |
Het |
Nwd1 |
G |
A |
8: 73,408,633 (GRCm39) |
C831Y |
probably damaging |
Het |
Or52r1c |
T |
C |
7: 102,735,058 (GRCm39) |
I111T |
probably damaging |
Het |
Or5t9 |
A |
G |
2: 86,659,950 (GRCm39) |
I285V |
probably benign |
Het |
P2ry14 |
A |
G |
3: 59,023,449 (GRCm39) |
S4P |
possibly damaging |
Het |
Parp4 |
A |
G |
14: 56,873,172 (GRCm39) |
|
probably benign |
Het |
Pate14 |
A |
T |
9: 36,549,873 (GRCm39) |
|
probably null |
Het |
Pclo |
A |
G |
5: 14,728,299 (GRCm39) |
|
probably benign |
Het |
Pclo |
T |
C |
5: 14,729,412 (GRCm39) |
|
probably benign |
Het |
Pcnt |
A |
T |
10: 76,240,429 (GRCm39) |
S1202T |
possibly damaging |
Het |
Pfkfb4 |
A |
G |
9: 108,856,825 (GRCm39) |
Y412C |
probably damaging |
Het |
Pgm2 |
T |
A |
5: 64,267,898 (GRCm39) |
V449D |
probably damaging |
Het |
Poldip3 |
T |
A |
15: 83,022,436 (GRCm39) |
D116V |
probably damaging |
Het |
Pom121 |
G |
T |
5: 135,410,686 (GRCm39) |
Q824K |
unknown |
Het |
Prkdc |
G |
T |
16: 15,649,146 (GRCm39) |
G3707* |
probably null |
Het |
Prr14l |
T |
C |
5: 33,001,560 (GRCm39) |
|
probably benign |
Het |
Ptbp2 |
T |
G |
3: 119,514,613 (GRCm39) |
I405L |
probably benign |
Het |
Rad21l |
A |
T |
2: 151,490,989 (GRCm39) |
|
probably benign |
Het |
Rbm6 |
G |
A |
9: 107,724,488 (GRCm39) |
Q488* |
probably null |
Het |
Rdh1 |
T |
A |
10: 127,600,652 (GRCm39) |
M225K |
probably benign |
Het |
Recql5 |
T |
C |
11: 115,819,209 (GRCm39) |
D119G |
probably benign |
Het |
Robo1 |
T |
C |
16: 72,810,013 (GRCm39) |
|
probably null |
Het |
Samd12 |
G |
A |
15: 53,723,567 (GRCm39) |
T42I |
probably benign |
Het |
Scn10a |
A |
T |
9: 119,442,766 (GRCm39) |
M1494K |
probably damaging |
Het |
Sec31a |
G |
A |
5: 100,523,099 (GRCm39) |
P864L |
probably benign |
Het |
Senp2 |
T |
C |
16: 21,855,320 (GRCm39) |
V344A |
probably benign |
Het |
Serpina5 |
G |
A |
12: 104,069,621 (GRCm39) |
D278N |
probably benign |
Het |
Sh3tc1 |
A |
T |
5: 35,860,806 (GRCm39) |
V1017D |
probably damaging |
Het |
Sin3a |
T |
A |
9: 57,004,179 (GRCm39) |
Y310* |
probably null |
Het |
Slc25a32 |
T |
C |
15: 38,960,940 (GRCm39) |
T248A |
probably benign |
Het |
Slc35e1 |
T |
C |
8: 73,246,415 (GRCm39) |
|
probably benign |
Het |
Slc4a10 |
G |
A |
2: 62,117,206 (GRCm39) |
V722M |
probably damaging |
Het |
Slco1a4 |
A |
G |
6: 141,776,586 (GRCm39) |
|
probably benign |
Het |
Smg6 |
T |
A |
11: 74,819,884 (GRCm39) |
Y52N |
probably damaging |
Het |
Sncb |
T |
G |
13: 54,913,400 (GRCm39) |
T33P |
probably damaging |
Het |
Spef2 |
A |
G |
15: 9,584,070 (GRCm39) |
|
probably null |
Het |
Spmip1 |
G |
T |
6: 29,478,169 (GRCm39) |
|
probably benign |
Het |
Sugp1 |
A |
G |
8: 70,512,013 (GRCm39) |
E203G |
probably damaging |
Het |
Suv39h2 |
A |
T |
2: 3,473,616 (GRCm39) |
C105S |
probably damaging |
Het |
Tlr1 |
A |
T |
5: 65,083,963 (GRCm39) |
F205I |
probably damaging |
Het |
Tnip1 |
A |
T |
11: 54,808,699 (GRCm39) |
M496K |
probably damaging |
Het |
Tnxb |
G |
A |
17: 34,937,219 (GRCm39) |
E2889K |
probably damaging |
Het |
Trim30b |
T |
A |
7: 104,015,010 (GRCm39) |
H126L |
possibly damaging |
Het |
Trpm7 |
A |
T |
2: 126,668,638 (GRCm39) |
Y759* |
probably null |
Het |
Ttc17 |
A |
G |
2: 94,153,465 (GRCm39) |
I1000T |
possibly damaging |
Het |
Ttc27 |
A |
T |
17: 75,025,710 (GRCm39) |
N61I |
probably benign |
Het |
Uba6 |
T |
C |
5: 86,260,609 (GRCm39) |
Y990C |
probably damaging |
Het |
Vav3 |
A |
G |
3: 109,571,756 (GRCm39) |
|
probably benign |
Het |
Vmn2r55 |
C |
T |
7: 12,404,945 (GRCm39) |
A153T |
possibly damaging |
Het |
Wars2 |
A |
G |
3: 99,123,865 (GRCm39) |
D242G |
probably damaging |
Het |
Xylt2 |
G |
A |
11: 94,560,762 (GRCm39) |
Q259* |
probably null |
Het |
Zfp27 |
G |
A |
7: 29,593,947 (GRCm39) |
P673S |
probably damaging |
Het |
Zgrf1 |
T |
C |
3: 127,378,309 (GRCm39) |
I1023T |
possibly damaging |
Het |
|
Other mutations in Rif1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00465:Rif1
|
APN |
2 |
52,011,019 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00711:Rif1
|
APN |
2 |
52,001,082 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00721:Rif1
|
APN |
2 |
52,009,129 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01085:Rif1
|
APN |
2 |
51,975,152 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01093:Rif1
|
APN |
2 |
51,985,960 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01107:Rif1
|
APN |
2 |
52,001,315 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01138:Rif1
|
APN |
2 |
52,001,534 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01844:Rif1
|
APN |
2 |
52,002,555 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02441:Rif1
|
APN |
2 |
51,995,527 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02448:Rif1
|
APN |
2 |
52,006,708 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02563:Rif1
|
APN |
2 |
51,967,077 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02704:Rif1
|
APN |
2 |
51,983,588 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02946:Rif1
|
APN |
2 |
52,000,137 (GRCm39) |
nonsense |
probably null |
|
IGL03060:Rif1
|
APN |
2 |
52,002,149 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03206:Rif1
|
APN |
2 |
51,993,634 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03263:Rif1
|
APN |
2 |
51,980,273 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03267:Rif1
|
APN |
2 |
51,967,000 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03280:Rif1
|
APN |
2 |
52,002,611 (GRCm39) |
missense |
probably benign |
0.32 |
hifi
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
nietzsche
|
UTSW |
2 |
51,967,032 (GRCm39) |
missense |
probably benign |
0.08 |
PIT4305001:Rif1
|
UTSW |
2 |
52,001,970 (GRCm39) |
missense |
|
|
R0017:Rif1
|
UTSW |
2 |
52,006,686 (GRCm39) |
missense |
probably benign |
0.18 |
R0017:Rif1
|
UTSW |
2 |
52,006,686 (GRCm39) |
missense |
probably benign |
0.18 |
R0060:Rif1
|
UTSW |
2 |
52,001,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Rif1
|
UTSW |
2 |
52,001,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R0104:Rif1
|
UTSW |
2 |
52,000,104 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0268:Rif1
|
UTSW |
2 |
51,980,298 (GRCm39) |
critical splice donor site |
probably null |
|
R0276:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0278:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0288:Rif1
|
UTSW |
2 |
52,000,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R0314:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0345:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0346:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0383:Rif1
|
UTSW |
2 |
51,975,153 (GRCm39) |
missense |
probably damaging |
0.96 |
R0384:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0387:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0388:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0456:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0477:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0505:Rif1
|
UTSW |
2 |
52,000,749 (GRCm39) |
missense |
probably damaging |
0.99 |
R0510:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0512:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0633:Rif1
|
UTSW |
2 |
52,002,575 (GRCm39) |
missense |
probably benign |
0.00 |
R0637:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0638:Rif1
|
UTSW |
2 |
52,001,600 (GRCm39) |
missense |
probably benign |
0.12 |
R0666:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0675:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0707:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0726:Rif1
|
UTSW |
2 |
52,000,365 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0743:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0744:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0938:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0939:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0940:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0941:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0942:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R0943:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1006:Rif1
|
UTSW |
2 |
51,975,041 (GRCm39) |
missense |
probably damaging |
0.99 |
R1052:Rif1
|
UTSW |
2 |
52,001,574 (GRCm39) |
missense |
probably benign |
0.01 |
R1061:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1175:Rif1
|
UTSW |
2 |
51,997,640 (GRCm39) |
unclassified |
probably benign |
|
R1183:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1184:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1271:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1332:Rif1
|
UTSW |
2 |
51,968,326 (GRCm39) |
missense |
probably benign |
0.06 |
R1336:Rif1
|
UTSW |
2 |
51,968,326 (GRCm39) |
missense |
probably benign |
0.06 |
R1351:Rif1
|
UTSW |
2 |
52,001,567 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1517:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1527:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1560:Rif1
|
UTSW |
2 |
52,001,143 (GRCm39) |
missense |
probably damaging |
1.00 |
R1563:Rif1
|
UTSW |
2 |
51,963,235 (GRCm39) |
missense |
probably damaging |
0.99 |
R1571:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1625:Rif1
|
UTSW |
2 |
51,993,652 (GRCm39) |
missense |
probably benign |
0.25 |
R1679:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1689:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1731:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1744:Rif1
|
UTSW |
2 |
52,002,404 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1746:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1748:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R1831:Rif1
|
UTSW |
2 |
51,968,507 (GRCm39) |
nonsense |
probably null |
|
R1902:Rif1
|
UTSW |
2 |
52,006,685 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1964:Rif1
|
UTSW |
2 |
51,988,421 (GRCm39) |
missense |
probably benign |
0.01 |
R1978:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2000:Rif1
|
UTSW |
2 |
51,971,310 (GRCm39) |
missense |
probably damaging |
0.99 |
R2030:Rif1
|
UTSW |
2 |
51,982,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R2056:Rif1
|
UTSW |
2 |
51,983,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R2106:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2109:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2125:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2126:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2145:Rif1
|
UTSW |
2 |
52,001,412 (GRCm39) |
missense |
possibly damaging |
0.63 |
R2152:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2153:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2213:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2327:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2512:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2513:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2516:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2520:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R2905:Rif1
|
UTSW |
2 |
51,988,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R3005:Rif1
|
UTSW |
2 |
51,972,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R3155:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R3156:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R3429:Rif1
|
UTSW |
2 |
52,000,336 (GRCm39) |
unclassified |
probably benign |
|
R3707:Rif1
|
UTSW |
2 |
51,983,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3907:Rif1
|
UTSW |
2 |
52,002,557 (GRCm39) |
missense |
probably benign |
0.03 |
R3978:Rif1
|
UTSW |
2 |
52,006,759 (GRCm39) |
critical splice donor site |
probably null |
|
R4023:Rif1
|
UTSW |
2 |
52,011,099 (GRCm39) |
missense |
probably benign |
0.01 |
R4052:Rif1
|
UTSW |
2 |
51,988,483 (GRCm39) |
nonsense |
probably null |
|
R4668:Rif1
|
UTSW |
2 |
52,001,964 (GRCm39) |
missense |
probably benign |
0.01 |
R4674:Rif1
|
UTSW |
2 |
51,996,954 (GRCm39) |
missense |
probably null |
1.00 |
R4715:Rif1
|
UTSW |
2 |
51,963,151 (GRCm39) |
utr 5 prime |
probably benign |
|
R4766:Rif1
|
UTSW |
2 |
51,988,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R4783:Rif1
|
UTSW |
2 |
52,002,759 (GRCm39) |
missense |
probably damaging |
0.96 |
R4785:Rif1
|
UTSW |
2 |
52,002,759 (GRCm39) |
missense |
probably damaging |
0.96 |
R4869:Rif1
|
UTSW |
2 |
51,983,623 (GRCm39) |
intron |
probably benign |
|
R4911:Rif1
|
UTSW |
2 |
52,000,530 (GRCm39) |
missense |
probably damaging |
0.98 |
R4951:Rif1
|
UTSW |
2 |
51,974,998 (GRCm39) |
splice site |
probably null |
|
R5044:Rif1
|
UTSW |
2 |
51,999,940 (GRCm39) |
missense |
probably damaging |
0.99 |
R5088:Rif1
|
UTSW |
2 |
51,982,307 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5151:Rif1
|
UTSW |
2 |
52,010,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R5187:Rif1
|
UTSW |
2 |
51,971,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R5222:Rif1
|
UTSW |
2 |
51,967,032 (GRCm39) |
missense |
probably benign |
0.08 |
R5243:Rif1
|
UTSW |
2 |
52,001,836 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5436:Rif1
|
UTSW |
2 |
52,010,983 (GRCm39) |
intron |
probably benign |
|
R5476:Rif1
|
UTSW |
2 |
51,979,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R5496:Rif1
|
UTSW |
2 |
51,988,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R5641:Rif1
|
UTSW |
2 |
52,011,170 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5883:Rif1
|
UTSW |
2 |
51,995,651 (GRCm39) |
critical splice donor site |
probably null |
|
R5987:Rif1
|
UTSW |
2 |
51,985,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R5990:Rif1
|
UTSW |
2 |
51,985,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R5992:Rif1
|
UTSW |
2 |
51,985,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R6019:Rif1
|
UTSW |
2 |
51,985,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R6020:Rif1
|
UTSW |
2 |
51,985,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R6255:Rif1
|
UTSW |
2 |
51,975,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R6342:Rif1
|
UTSW |
2 |
52,009,168 (GRCm39) |
missense |
probably damaging |
0.97 |
R6364:Rif1
|
UTSW |
2 |
51,997,681 (GRCm39) |
missense |
probably damaging |
0.97 |
R6747:Rif1
|
UTSW |
2 |
51,968,275 (GRCm39) |
splice site |
probably null |
|
R6928:Rif1
|
UTSW |
2 |
51,985,973 (GRCm39) |
missense |
probably damaging |
1.00 |
R6954:Rif1
|
UTSW |
2 |
52,002,703 (GRCm39) |
missense |
probably benign |
0.00 |
R7003:Rif1
|
UTSW |
2 |
51,967,001 (GRCm39) |
missense |
probably benign |
0.06 |
R7310:Rif1
|
UTSW |
2 |
51,995,631 (GRCm39) |
missense |
probably benign |
0.12 |
R7549:Rif1
|
UTSW |
2 |
51,968,519 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7603:Rif1
|
UTSW |
2 |
51,966,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R7673:Rif1
|
UTSW |
2 |
51,978,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R7741:Rif1
|
UTSW |
2 |
51,975,153 (GRCm39) |
missense |
probably damaging |
0.96 |
R7777:Rif1
|
UTSW |
2 |
52,006,368 (GRCm39) |
missense |
probably benign |
0.00 |
R7910:Rif1
|
UTSW |
2 |
51,968,399 (GRCm39) |
nonsense |
probably null |
|
R7962:Rif1
|
UTSW |
2 |
51,964,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R8264:Rif1
|
UTSW |
2 |
51,980,290 (GRCm39) |
missense |
noncoding transcript |
|
R8390:Rif1
|
UTSW |
2 |
52,000,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R8479:Rif1
|
UTSW |
2 |
52,002,563 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8490:Rif1
|
UTSW |
2 |
52,001,011 (GRCm39) |
missense |
probably damaging |
0.96 |
R8762:Rif1
|
UTSW |
2 |
52,001,742 (GRCm39) |
missense |
|
|
R8785:Rif1
|
UTSW |
2 |
52,000,493 (GRCm39) |
missense |
probably benign |
0.06 |
R8890:Rif1
|
UTSW |
2 |
51,988,875 (GRCm39) |
missense |
probably damaging |
0.99 |
R9081:Rif1
|
UTSW |
2 |
52,000,989 (GRCm39) |
missense |
probably damaging |
0.99 |
R9225:Rif1
|
UTSW |
2 |
52,001,862 (GRCm39) |
missense |
probably benign |
0.22 |
R9284:Rif1
|
UTSW |
2 |
51,998,564 (GRCm39) |
missense |
probably benign |
0.00 |
R9300:Rif1
|
UTSW |
2 |
52,001,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R9366:Rif1
|
UTSW |
2 |
52,010,356 (GRCm39) |
missense |
|
|
R9477:Rif1
|
UTSW |
2 |
52,001,342 (GRCm39) |
missense |
probably benign |
0.02 |
R9522:Rif1
|
UTSW |
2 |
51,971,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R9573:Rif1
|
UTSW |
2 |
52,000,466 (GRCm39) |
missense |
probably benign |
0.29 |
R9630:Rif1
|
UTSW |
2 |
51,979,607 (GRCm39) |
missense |
probably damaging |
1.00 |
X0064:Rif1
|
UTSW |
2 |
51,984,645 (GRCm39) |
missense |
probably damaging |
0.96 |
X0064:Rif1
|
UTSW |
2 |
51,964,327 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Rif1
|
UTSW |
2 |
51,978,660 (GRCm39) |
missense |
probably damaging |
1.00 |
|