Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf3 |
C |
T |
16: 20,371,201 (GRCm39) |
H436Y |
possibly damaging |
Het |
Acad10 |
A |
T |
5: 121,772,864 (GRCm39) |
H472Q |
possibly damaging |
Het |
Ano8 |
G |
A |
8: 71,935,024 (GRCm39) |
R393C |
probably damaging |
Het |
Arhgap18 |
T |
A |
10: 26,736,646 (GRCm39) |
V163E |
probably damaging |
Het |
AW209491 |
C |
T |
13: 14,812,365 (GRCm39) |
A406V |
probably benign |
Het |
Brix1 |
C |
T |
15: 10,476,675 (GRCm39) |
R267H |
probably benign |
Het |
Cacng5 |
T |
C |
11: 107,775,214 (GRCm39) |
M52V |
probably benign |
Het |
Casz1 |
T |
C |
4: 149,031,495 (GRCm39) |
C1249R |
probably damaging |
Het |
Cenpj |
C |
T |
14: 56,772,272 (GRCm39) |
S1086N |
probably benign |
Het |
Chi3l1 |
T |
C |
1: 134,117,310 (GRCm39) |
F367S |
probably benign |
Het |
Copg2 |
A |
T |
6: 30,787,868 (GRCm39) |
I610N |
possibly damaging |
Het |
Cpa6 |
T |
C |
1: 10,665,868 (GRCm39) |
K57E |
possibly damaging |
Het |
D5Ertd579e |
C |
T |
5: 36,787,036 (GRCm39) |
A111T |
possibly damaging |
Het |
Dgat2 |
A |
G |
7: 98,803,838 (GRCm39) |
M361T |
probably benign |
Het |
Dnm3 |
G |
T |
1: 161,962,070 (GRCm39) |
F46L |
probably damaging |
Het |
Dph7 |
T |
A |
2: 24,853,552 (GRCm39) |
C122* |
probably null |
Het |
Dspp |
A |
T |
5: 104,325,905 (GRCm39) |
D756V |
unknown |
Het |
Efcab3 |
T |
C |
11: 104,933,728 (GRCm39) |
|
probably null |
Het |
Ep300 |
T |
A |
15: 81,525,583 (GRCm39) |
M1469K |
unknown |
Het |
Fsip2 |
T |
C |
2: 82,818,283 (GRCm39) |
I4672T |
possibly damaging |
Het |
Gapdh |
A |
T |
6: 125,139,996 (GRCm39) |
L67* |
probably null |
Het |
Gpr75 |
A |
G |
11: 30,841,640 (GRCm39) |
R182G |
probably benign |
Het |
Gsr |
G |
T |
8: 34,183,835 (GRCm39) |
A366S |
probably damaging |
Het |
Gypc |
A |
G |
18: 32,663,248 (GRCm39) |
I33T |
probably damaging |
Het |
Hapln1 |
A |
G |
13: 89,756,219 (GRCm39) |
D341G |
probably benign |
Het |
Hnrnpd |
A |
G |
5: 100,115,095 (GRCm39) |
S148P |
probably benign |
Het |
Hydin |
A |
T |
8: 111,293,252 (GRCm39) |
T3450S |
probably benign |
Het |
Kif20b |
T |
C |
19: 34,927,864 (GRCm39) |
V1002A |
probably benign |
Het |
Kif5c |
T |
C |
2: 49,625,521 (GRCm39) |
V597A |
probably benign |
Het |
Kntc1 |
A |
G |
5: 123,900,579 (GRCm39) |
T226A |
probably benign |
Het |
Krt75 |
C |
A |
15: 101,482,158 (GRCm39) |
V37L |
probably benign |
Het |
L3mbtl2 |
A |
G |
15: 81,571,143 (GRCm39) |
I668V |
probably benign |
Het |
Lrp1b |
G |
A |
2: 41,192,982 (GRCm39) |
A480V |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 41,366,821 (GRCm39) |
D485V |
probably damaging |
Het |
Lrrc37a |
T |
C |
11: 103,347,422 (GRCm39) |
H3091R |
unknown |
Het |
Msi1 |
A |
G |
5: 115,589,550 (GRCm39) |
Y361C |
probably damaging |
Het |
Mtus1 |
G |
T |
8: 41,536,077 (GRCm39) |
N546K |
probably benign |
Het |
Mup17 |
T |
A |
4: 61,511,936 (GRCm39) |
T113S |
probably benign |
Het |
Myh11 |
T |
A |
16: 14,023,938 (GRCm39) |
D1479V |
probably damaging |
Het |
Ncor1 |
C |
T |
11: 62,263,987 (GRCm39) |
E198K |
probably benign |
Het |
Nrde2 |
A |
G |
12: 100,098,501 (GRCm39) |
V722A |
probably benign |
Het |
Or13a28 |
T |
C |
7: 140,217,925 (GRCm39) |
F104L |
probably benign |
Het |
Or51f23 |
C |
T |
7: 102,453,491 (GRCm39) |
R269* |
probably null |
Het |
Or5ac24 |
C |
T |
16: 59,165,798 (GRCm39) |
D89N |
possibly damaging |
Het |
Otog |
A |
G |
7: 45,938,374 (GRCm39) |
M2028V |
probably benign |
Het |
Paox |
T |
A |
7: 139,711,655 (GRCm39) |
V169E |
probably damaging |
Het |
Pcsk9 |
T |
G |
4: 106,314,073 (GRCm39) |
D174A |
probably benign |
Het |
Pde4b |
A |
G |
4: 102,427,966 (GRCm39) |
E41G |
possibly damaging |
Het |
Pip4k2c |
A |
G |
10: 127,034,943 (GRCm39) |
I419T |
probably damaging |
Het |
Plekhg3 |
G |
T |
12: 76,624,715 (GRCm39) |
E1186* |
probably null |
Het |
Pole |
C |
A |
5: 110,472,380 (GRCm39) |
P1548T |
probably benign |
Het |
Pole |
C |
T |
5: 110,472,381 (GRCm39) |
P1548L |
probably benign |
Het |
Polq |
A |
G |
16: 36,882,126 (GRCm39) |
E1430G |
probably damaging |
Het |
Potefam3c |
A |
T |
8: 69,881,966 (GRCm39) |
C337S |
probably benign |
Het |
Pramel47 |
G |
A |
5: 95,488,072 (GRCm39) |
S2N |
probably damaging |
Het |
Ptgr2 |
T |
C |
12: 84,344,920 (GRCm39) |
S98P |
probably damaging |
Het |
Ralgapa1 |
A |
G |
12: 55,730,827 (GRCm39) |
Y1903H |
possibly damaging |
Het |
Rasgrp1 |
T |
C |
2: 117,122,376 (GRCm39) |
D338G |
probably damaging |
Het |
Rnase13 |
C |
T |
14: 52,159,860 (GRCm39) |
C93Y |
probably damaging |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
S100z |
T |
A |
13: 95,613,934 (GRCm39) |
M59L |
probably benign |
Het |
Ska1 |
T |
A |
18: 74,332,992 (GRCm39) |
D142V |
probably benign |
Het |
Slc16a3 |
T |
C |
11: 120,847,931 (GRCm39) |
|
probably null |
Het |
Snd1 |
T |
C |
6: 28,880,233 (GRCm39) |
V669A |
probably benign |
Het |
Snrpd3 |
A |
T |
10: 75,368,029 (GRCm39) |
T49S |
probably damaging |
Het |
Sort1 |
T |
C |
3: 108,264,549 (GRCm39) |
L856P |
possibly damaging |
Het |
Srek1ip1 |
T |
A |
13: 104,970,830 (GRCm39) |
|
probably null |
Het |
Ssrp1 |
T |
C |
2: 84,875,796 (GRCm39) |
S552P |
probably damaging |
Het |
Stab2 |
A |
G |
10: 86,838,886 (GRCm39) |
V60A |
probably benign |
Het |
Stard9 |
GCCC |
GCC |
2: 120,524,196 (GRCm39) |
|
probably null |
Het |
Tll1 |
A |
C |
8: 64,494,525 (GRCm39) |
H743Q |
possibly damaging |
Het |
Tpo |
G |
T |
12: 30,144,980 (GRCm39) |
R590S |
possibly damaging |
Het |
Trbv12-1 |
A |
T |
6: 41,090,780 (GRCm39) |
T51S |
probably benign |
Het |
Trbv30 |
C |
T |
6: 41,258,708 (GRCm39) |
A40V |
probably benign |
Het |
Tulp4 |
T |
A |
17: 6,283,490 (GRCm39) |
V1173E |
possibly damaging |
Het |
Upk1a |
A |
T |
7: 30,311,810 (GRCm39) |
|
probably null |
Het |
Vinac1 |
T |
C |
2: 128,879,610 (GRCm39) |
Q772R |
probably benign |
Het |
Vmn1r199 |
A |
G |
13: 22,566,769 (GRCm39) |
D21G |
possibly damaging |
Het |
Vmn2r7 |
T |
C |
3: 64,623,643 (GRCm39) |
T317A |
probably damaging |
Het |
Wdfy3 |
A |
G |
5: 101,997,289 (GRCm39) |
V3112A |
probably damaging |
Het |
Zbtb8os |
T |
C |
4: 129,234,542 (GRCm39) |
V40A |
possibly damaging |
Het |
Zfp1002 |
T |
A |
2: 150,097,132 (GRCm39) |
H99L |
probably damaging |
Het |
Zwint |
A |
G |
10: 72,492,685 (GRCm39) |
K108E |
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 |
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 |
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 |
|