Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr3 |
A |
T |
1: 90,141,565 (GRCm39) |
Y8F |
probably benign |
Het |
Acy1 |
T |
C |
9: 106,312,816 (GRCm39) |
E175G |
probably damaging |
Het |
Add2 |
T |
C |
6: 86,075,580 (GRCm39) |
L243P |
probably damaging |
Het |
Adsl |
A |
G |
15: 80,851,863 (GRCm39) |
D407G |
probably damaging |
Het |
Afg3l1 |
T |
G |
8: 124,221,575 (GRCm39) |
I478S |
probably damaging |
Het |
Aoc1l1 |
T |
A |
6: 48,953,473 (GRCm39) |
I466N |
probably damaging |
Het |
Arfrp1 |
T |
C |
2: 181,001,487 (GRCm39) |
T108A |
probably benign |
Het |
Art5 |
A |
G |
7: 101,747,407 (GRCm39) |
L124P |
possibly damaging |
Het |
Asap2 |
A |
T |
12: 21,162,084 (GRCm39) |
T14S |
probably damaging |
Het |
Atp2c2 |
A |
G |
8: 120,482,841 (GRCm39) |
N901S |
probably benign |
Het |
Bbs12 |
G |
T |
3: 37,375,309 (GRCm39) |
E586* |
probably null |
Het |
Bicd2 |
G |
T |
13: 49,533,052 (GRCm39) |
C546F |
probably damaging |
Het |
Bid |
A |
T |
6: 120,877,215 (GRCm39) |
L42Q |
probably damaging |
Het |
Bpifb9a |
A |
G |
2: 154,102,055 (GRCm39) |
K51E |
probably benign |
Het |
Calcr |
G |
T |
6: 3,687,615 (GRCm39) |
T424K |
probably benign |
Het |
Cd46 |
A |
G |
1: 194,744,721 (GRCm39) |
I339T |
probably benign |
Het |
Chek1 |
C |
A |
9: 36,635,279 (GRCm39) |
V35F |
probably damaging |
Het |
Cntn3 |
A |
G |
6: 102,183,498 (GRCm39) |
I719T |
probably damaging |
Het |
Cyb5r1 |
T |
C |
1: 134,337,363 (GRCm39) |
I163T |
possibly damaging |
Het |
Cyp2d26 |
A |
T |
15: 82,676,907 (GRCm39) |
|
probably null |
Het |
Dclk1 |
A |
G |
3: 55,154,633 (GRCm39) |
Y21C |
probably damaging |
Het |
Dgcr2 |
G |
A |
16: 17,709,351 (GRCm39) |
|
probably null |
Het |
Dhx38 |
T |
C |
8: 110,287,306 (GRCm39) |
S221G |
probably benign |
Het |
Dis3l |
T |
A |
9: 64,214,545 (GRCm39) |
N981I |
probably benign |
Het |
Dnah3 |
C |
T |
7: 119,551,236 (GRCm39) |
V3028I |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,026,149 (GRCm39) |
Y3448C |
probably benign |
Het |
Dok5 |
G |
A |
2: 170,642,816 (GRCm39) |
G38D |
probably damaging |
Het |
Epb41l1 |
A |
G |
2: 156,356,048 (GRCm39) |
D528G |
probably damaging |
Het |
Fat4 |
A |
T |
3: 39,037,544 (GRCm39) |
Y3732F |
probably damaging |
Het |
Fcsk |
T |
A |
8: 111,615,704 (GRCm39) |
T542S |
probably benign |
Het |
Fgfr4 |
A |
T |
13: 55,314,777 (GRCm39) |
Y640F |
probably damaging |
Het |
Foxo6 |
T |
A |
4: 120,125,811 (GRCm39) |
D328V |
probably benign |
Het |
Foxp1 |
A |
G |
6: 98,993,502 (GRCm39) |
L134P |
probably damaging |
Het |
Frem2 |
G |
A |
3: 53,424,450 (GRCm39) |
R2996* |
probably null |
Het |
Garem2 |
T |
C |
5: 30,313,297 (GRCm39) |
S54P |
probably damaging |
Het |
Gcn1 |
T |
A |
5: 115,747,888 (GRCm39) |
I1765N |
probably benign |
Het |
Gm4787 |
T |
A |
12: 81,423,993 (GRCm39) |
I722F |
probably benign |
Het |
Gpc6 |
G |
T |
14: 117,163,504 (GRCm39) |
A53S |
probably benign |
Het |
Gtpbp8 |
A |
G |
16: 44,560,390 (GRCm39) |
|
probably null |
Het |
H2-Q2 |
T |
C |
17: 35,564,252 (GRCm39) |
|
probably null |
Het |
Hapln2 |
C |
A |
3: 87,930,920 (GRCm39) |
R157L |
probably benign |
Het |
Hemgn |
C |
A |
4: 46,396,607 (GRCm39) |
E210* |
probably null |
Het |
Hpse |
T |
A |
5: 100,839,269 (GRCm39) |
K360* |
probably null |
Het |
Iqcj |
A |
T |
3: 67,962,643 (GRCm39) |
E68V |
probably damaging |
Het |
Kat2a |
T |
C |
11: 100,603,172 (GRCm39) |
|
probably benign |
Het |
Kat6b |
A |
T |
14: 21,718,735 (GRCm39) |
H1138L |
probably benign |
Het |
Kcnab1 |
A |
T |
3: 65,278,861 (GRCm39) |
I371F |
probably damaging |
Het |
Klhl30 |
C |
A |
1: 91,285,546 (GRCm39) |
A356D |
probably benign |
Het |
Klra3 |
G |
C |
6: 130,310,107 (GRCm39) |
R138G |
probably benign |
Het |
Micu1 |
G |
T |
10: 59,699,110 (GRCm39) |
M468I |
probably benign |
Het |
Mrc1 |
A |
G |
2: 14,332,675 (GRCm39) |
T1292A |
probably damaging |
Het |
Myh8 |
G |
A |
11: 67,185,295 (GRCm39) |
E849K |
probably damaging |
Het |
Myom3 |
G |
T |
4: 135,530,544 (GRCm39) |
R1152L |
probably benign |
Het |
Nedd4l |
T |
A |
18: 65,343,401 (GRCm39) |
H820Q |
probably damaging |
Het |
Nlrp4g |
T |
A |
9: 124,353,339 (GRCm38) |
|
noncoding transcript |
Het |
Oga |
A |
T |
19: 45,746,461 (GRCm39) |
Y779* |
probably null |
Het |
Or13p5 |
C |
T |
4: 118,592,446 (GRCm39) |
A240V |
possibly damaging |
Het |
Or1m1 |
T |
C |
9: 18,666,391 (GRCm39) |
D180G |
probably damaging |
Het |
Or2a51 |
A |
G |
6: 43,179,003 (GRCm39) |
I142V |
probably benign |
Het |
Or51a39 |
G |
T |
7: 102,362,788 (GRCm39) |
H277Q |
probably benign |
Het |
Or52j3 |
A |
T |
7: 102,835,847 (GRCm39) |
D13V |
probably benign |
Het |
Or8b49 |
G |
T |
9: 38,505,707 (GRCm39) |
L63F |
probably damaging |
Het |
Or8g54 |
A |
T |
9: 39,706,943 (GRCm39) |
I91F |
probably benign |
Het |
Or9s23 |
T |
C |
1: 92,501,630 (GRCm39) |
S246P |
probably damaging |
Het |
Otop1 |
T |
A |
5: 38,460,194 (GRCm39) |
M587K |
probably damaging |
Het |
Pgm5 |
T |
A |
19: 24,812,179 (GRCm39) |
I118F |
probably damaging |
Het |
Phc2 |
A |
G |
4: 128,638,859 (GRCm39) |
*41W |
probably null |
Het |
Phf8-ps |
T |
A |
17: 33,285,908 (GRCm39) |
D298V |
probably damaging |
Het |
Piezo2 |
A |
T |
18: 63,247,112 (GRCm39) |
M532K |
probably damaging |
Het |
Pjvk |
A |
T |
2: 76,488,713 (GRCm39) |
I295F |
probably benign |
Het |
Popdc2 |
A |
G |
16: 38,183,482 (GRCm39) |
N155S |
possibly damaging |
Het |
Ppp4r3a |
G |
T |
12: 101,008,826 (GRCm39) |
N684K |
probably damaging |
Het |
Prpf4b |
T |
A |
13: 35,084,402 (GRCm39) |
M930K |
probably benign |
Het |
Ptpn12 |
C |
A |
5: 21,207,466 (GRCm39) |
Q297H |
probably damaging |
Het |
Ptprz1 |
C |
A |
6: 23,030,670 (GRCm39) |
L1010I |
probably damaging |
Het |
Rabepk |
A |
T |
2: 34,674,562 (GRCm39) |
D232E |
possibly damaging |
Het |
Rad51ap2 |
A |
G |
12: 11,507,986 (GRCm39) |
H636R |
probably benign |
Het |
Rb1 |
T |
C |
14: 73,526,165 (GRCm39) |
T169A |
probably benign |
Het |
Rcc2 |
T |
C |
4: 140,444,428 (GRCm39) |
L373P |
probably damaging |
Het |
Rrbp1 |
A |
G |
2: 143,796,118 (GRCm39) |
L1200P |
possibly damaging |
Het |
Sdk1 |
A |
G |
5: 141,778,699 (GRCm39) |
N226D |
probably damaging |
Het |
Selenbp1 |
G |
A |
3: 94,851,441 (GRCm39) |
R398H |
probably damaging |
Het |
Selenoo |
A |
G |
15: 88,983,485 (GRCm39) |
M509V |
probably benign |
Het |
Sidt2 |
T |
C |
9: 45,856,638 (GRCm39) |
D477G |
probably damaging |
Het |
Slc2a5 |
T |
G |
4: 150,210,095 (GRCm39) |
S27A |
probably damaging |
Het |
Slc30a5 |
A |
T |
13: 100,940,457 (GRCm39) |
H619Q |
probably damaging |
Het |
Slc5a9 |
A |
G |
4: 111,750,420 (GRCm39) |
I146T |
possibly damaging |
Het |
Slc6a1 |
G |
T |
6: 114,284,731 (GRCm39) |
G263V |
probably damaging |
Het |
Slmap |
A |
G |
14: 26,139,402 (GRCm39) |
Y771H |
probably damaging |
Het |
Snx29 |
A |
G |
16: 11,218,707 (GRCm39) |
D181G |
possibly damaging |
Het |
Spata31d1c |
G |
A |
13: 65,181,779 (GRCm39) |
|
probably null |
Het |
Stat5a |
C |
A |
11: 100,764,916 (GRCm39) |
T213N |
probably benign |
Het |
Stt3a |
A |
T |
9: 36,659,292 (GRCm39) |
V349D |
probably damaging |
Het |
Tcf20 |
A |
T |
15: 82,739,803 (GRCm39) |
D549E |
probably damaging |
Het |
Thbs2 |
T |
A |
17: 14,893,471 (GRCm39) |
D903V |
probably damaging |
Het |
Tln2 |
T |
C |
9: 67,209,842 (GRCm39) |
T432A |
probably damaging |
Het |
Tmc1 |
A |
T |
19: 20,834,039 (GRCm39) |
N241K |
probably benign |
Het |
Tmem260 |
G |
T |
14: 48,715,066 (GRCm39) |
R240L |
possibly damaging |
Het |
Tnfaip6 |
A |
T |
2: 51,933,742 (GRCm39) |
E32D |
probably damaging |
Het |
Trpa1 |
A |
T |
1: 14,969,625 (GRCm39) |
H381Q |
probably damaging |
Het |
Tsen2 |
T |
C |
6: 115,524,936 (GRCm39) |
I45T |
possibly damaging |
Het |
Ttc6 |
G |
A |
12: 57,752,338 (GRCm39) |
V1415I |
probably damaging |
Het |
Ttll7 |
G |
T |
3: 146,635,944 (GRCm39) |
R426L |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,570,482 (GRCm39) |
S26804A |
probably damaging |
Het |
Ubqlnl |
A |
T |
7: 103,797,890 (GRCm39) |
C536S |
probably benign |
Het |
Vmn2r73 |
A |
G |
7: 85,506,936 (GRCm39) |
V792A |
probably benign |
Het |
Zfp345 |
T |
C |
2: 150,314,578 (GRCm39) |
T320A |
probably benign |
Het |
Zfp407 |
T |
C |
18: 84,227,774 (GRCm39) |
D1945G |
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 |
|
R0511: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 |
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 |
|