Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
C |
T |
5: 113,245,502 (GRCm39) |
V1584I |
probably benign |
Het |
Adamts12 |
A |
G |
15: 11,285,987 (GRCm39) |
D732G |
probably benign |
Het |
Agpat4 |
A |
G |
17: 12,370,637 (GRCm39) |
|
probably benign |
Het |
AI182371 |
T |
C |
2: 34,985,829 (GRCm39) |
D140G |
possibly damaging |
Het |
Apol11b |
T |
A |
15: 77,519,133 (GRCm39) |
T316S |
probably benign |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Bard1 |
T |
C |
1: 71,114,333 (GRCm39) |
E216G |
probably benign |
Het |
Bdp1 |
C |
A |
13: 100,186,376 (GRCm39) |
R1692L |
probably damaging |
Het |
Capn10 |
T |
C |
1: 92,871,141 (GRCm39) |
I101T |
probably damaging |
Het |
Ccdc175 |
C |
T |
12: 72,158,979 (GRCm39) |
M653I |
probably benign |
Het |
Ccdc9b |
C |
A |
2: 118,590,058 (GRCm39) |
R262L |
probably damaging |
Het |
Ccr8 |
G |
A |
9: 119,923,530 (GRCm39) |
C215Y |
probably damaging |
Het |
Cct3 |
T |
A |
3: 88,219,092 (GRCm39) |
L241* |
probably null |
Het |
Cd2ap |
A |
T |
17: 43,163,350 (GRCm39) |
I25N |
probably damaging |
Het |
Cdh19 |
T |
C |
1: 110,820,990 (GRCm39) |
K583E |
probably benign |
Het |
Cela3a |
A |
G |
4: 137,129,986 (GRCm39) |
S212P |
unknown |
Het |
Cfap44 |
T |
A |
16: 44,236,246 (GRCm39) |
|
probably null |
Het |
Clca3a1 |
A |
T |
3: 144,455,473 (GRCm39) |
L440Q |
probably damaging |
Het |
Crybg2 |
A |
G |
4: 133,816,663 (GRCm39) |
Y1676C |
probably damaging |
Het |
Dscam |
T |
C |
16: 96,445,188 (GRCm39) |
D1501G |
probably benign |
Het |
Eml6 |
C |
A |
11: 29,755,757 (GRCm39) |
L832F |
probably benign |
Het |
Enpp3 |
A |
G |
10: 24,649,825 (GRCm39) |
L867P |
probably damaging |
Het |
Erbb3 |
A |
G |
10: 128,422,107 (GRCm39) |
Y46H |
possibly damaging |
Het |
Fads3 |
T |
C |
19: 10,033,384 (GRCm39) |
I342T |
possibly damaging |
Het |
Flvcr1 |
A |
T |
1: 190,753,303 (GRCm39) |
S290T |
probably benign |
Het |
Fut9 |
A |
G |
4: 25,799,191 (GRCm39) |
|
probably benign |
Het |
Gad2 |
C |
T |
2: 22,512,679 (GRCm39) |
A2V |
probably damaging |
Het |
Gkn3 |
C |
T |
6: 87,360,507 (GRCm39) |
A163T |
probably damaging |
Het |
Gm10715 |
T |
G |
9: 3,038,073 (GRCm39) |
|
probably benign |
Het |
Herc1 |
T |
G |
9: 66,349,211 (GRCm39) |
D2023E |
probably benign |
Het |
Hsd3b3 |
A |
G |
3: 98,649,801 (GRCm39) |
L174P |
probably damaging |
Het |
Impg2 |
TACCACCACCACCACCACCACCACCA |
TACCACCACCACCACCACCACCA |
16: 56,078,302 (GRCm39) |
|
probably benign |
Het |
Iqcf3 |
A |
G |
9: 106,438,148 (GRCm39) |
|
probably null |
Het |
Kcna4 |
G |
A |
2: 107,126,888 (GRCm39) |
V541M |
probably damaging |
Het |
Kcnj11 |
T |
C |
7: 45,749,240 (GRCm39) |
T28A |
probably benign |
Het |
Kcnmb2 |
T |
A |
3: 32,236,016 (GRCm39) |
N88K |
probably damaging |
Het |
Kdm2a |
TTCCTCCTCCTCCTCCTCTTCCTCCTCCTC |
TTCCTCCTCCTCCTCTTCCTCCTCCTC |
19: 4,374,535 (GRCm39) |
|
probably benign |
Het |
Krt1c |
T |
C |
15: 101,722,395 (GRCm39) |
E430G |
probably damaging |
Het |
Lins1 |
C |
T |
7: 66,360,389 (GRCm39) |
L384F |
possibly damaging |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Mfge8 |
T |
C |
7: 78,784,273 (GRCm39) |
N389D |
probably damaging |
Het |
Mug1 |
C |
T |
6: 121,861,213 (GRCm39) |
T1278I |
probably benign |
Het |
Myh9 |
T |
C |
15: 77,692,077 (GRCm39) |
M161V |
probably damaging |
Het |
Myl7 |
T |
A |
11: 5,848,171 (GRCm39) |
Y61F |
probably benign |
Het |
Nlrp4d |
A |
T |
7: 10,096,706 (GRCm39) |
|
unknown |
Het |
Nol3 |
A |
G |
8: 106,008,565 (GRCm39) |
|
probably null |
Het |
Nup85 |
T |
A |
11: 115,468,751 (GRCm39) |
|
probably null |
Het |
Obscn |
T |
A |
11: 58,903,568 (GRCm39) |
T7619S |
probably damaging |
Het |
Or2t49 |
T |
A |
11: 58,392,494 (GRCm39) |
N296I |
probably damaging |
Het |
Or4k48 |
T |
C |
2: 111,476,226 (GRCm39) |
M39V |
probably benign |
Het |
Or52a24 |
C |
T |
7: 103,381,457 (GRCm39) |
T108I |
possibly damaging |
Het |
Or7g26 |
G |
A |
9: 19,230,141 (GRCm39) |
V104I |
probably benign |
Het |
Pax5 |
T |
A |
4: 44,679,494 (GRCm39) |
I184F |
probably damaging |
Het |
Pcdha7 |
T |
A |
18: 37,107,560 (GRCm39) |
V195D |
probably damaging |
Het |
Phf3 |
A |
T |
1: 30,853,020 (GRCm39) |
|
probably benign |
Het |
Pla2g15 |
G |
T |
8: 106,889,703 (GRCm39) |
G325V |
probably damaging |
Het |
Ppp1r21 |
T |
C |
17: 88,880,043 (GRCm39) |
F487L |
probably benign |
Het |
Ppp1r9a |
A |
G |
6: 5,157,016 (GRCm39) |
I965V |
probably benign |
Het |
Ptpru |
A |
G |
4: 131,548,275 (GRCm39) |
V74A |
probably damaging |
Het |
Rps25 |
T |
A |
9: 44,320,046 (GRCm39) |
Y23N |
possibly damaging |
Het |
Ryr1 |
T |
C |
7: 28,785,258 (GRCm39) |
D1811G |
probably damaging |
Het |
Scamp5 |
T |
G |
9: 57,359,319 (GRCm39) |
|
probably null |
Het |
Senp1 |
T |
C |
15: 97,943,777 (GRCm39) |
D602G |
probably damaging |
Het |
Sh2b2 |
T |
G |
5: 136,260,811 (GRCm39) |
D135A |
probably damaging |
Het |
Slc26a8 |
G |
A |
17: 28,857,635 (GRCm39) |
T836M |
probably benign |
Het |
Slfn4 |
T |
G |
11: 83,077,647 (GRCm39) |
I145S |
possibly damaging |
Het |
Spag6l |
G |
A |
16: 16,595,254 (GRCm39) |
T377I |
probably benign |
Het |
Spdye4b |
T |
C |
5: 143,182,089 (GRCm39) |
F129S |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,447,514 (GRCm39) |
G2360E |
probably benign |
Het |
Taar2 |
A |
T |
10: 23,816,669 (GRCm39) |
I70F |
probably damaging |
Het |
Taar7e |
A |
G |
10: 23,914,464 (GRCm39) |
N318S |
probably damaging |
Het |
Tor1a |
C |
A |
2: 30,857,742 (GRCm39) |
R42L |
probably benign |
Het |
Trdn |
A |
T |
10: 33,350,502 (GRCm39) |
Q690H |
probably benign |
Het |
Trim56 |
C |
A |
5: 137,141,579 (GRCm39) |
V646L |
probably benign |
Het |
Tspan15 |
T |
A |
10: 62,027,323 (GRCm39) |
K165I |
probably benign |
Het |
Usp24 |
A |
G |
4: 106,273,245 (GRCm39) |
Y2210C |
probably damaging |
Het |
Usp45 |
A |
G |
4: 21,797,307 (GRCm39) |
T76A |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,785,506 (GRCm39) |
|
probably null |
Het |
Zfp512b |
T |
C |
2: 181,226,888 (GRCm39) |
|
probably benign |
Het |
Zyx |
C |
A |
6: 42,333,093 (GRCm39) |
|
probably null |
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 |
|
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 |
|