Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933409G03Rik |
A |
C |
2: 68,423,934 (GRCm39) |
M46L |
|
Het |
Aars2 |
A |
G |
17: 45,827,410 (GRCm39) |
E484G |
probably benign |
Het |
Abcd2 |
C |
T |
15: 91,075,825 (GRCm39) |
|
probably benign |
Het |
Acap2 |
A |
G |
16: 30,929,901 (GRCm39) |
S361P |
possibly damaging |
Het |
Arap2 |
T |
C |
5: 62,887,900 (GRCm39) |
E482G |
probably benign |
Het |
Axin2 |
G |
T |
11: 108,833,782 (GRCm39) |
L576F |
possibly damaging |
Het |
B4galt2 |
T |
A |
4: 117,738,123 (GRCm39) |
Y161F |
probably damaging |
Het |
Cdh3 |
A |
T |
8: 107,266,425 (GRCm39) |
|
probably null |
Het |
Cfap61 |
A |
T |
2: 145,971,149 (GRCm39) |
I920F |
probably benign |
Het |
Chaf1b |
T |
C |
16: 93,681,394 (GRCm39) |
I4T |
probably benign |
Het |
Clptm1 |
T |
C |
7: 19,371,449 (GRCm39) |
N328S |
probably benign |
Het |
Cthrc1 |
A |
G |
15: 38,947,689 (GRCm39) |
N136S |
probably benign |
Het |
Dlec1 |
G |
T |
9: 118,971,652 (GRCm39) |
R1279L |
probably damaging |
Het |
Dnah5 |
A |
T |
15: 28,366,293 (GRCm39) |
T2669S |
possibly damaging |
Het |
Efcab14 |
C |
A |
4: 115,610,208 (GRCm39) |
L190I |
probably damaging |
Het |
Eml6 |
A |
T |
11: 29,769,076 (GRCm39) |
C690S |
probably damaging |
Het |
Fignl1 |
T |
C |
11: 11,751,483 (GRCm39) |
E524G |
probably damaging |
Het |
Fmo4 |
A |
G |
1: 162,631,238 (GRCm39) |
V243A |
probably benign |
Het |
Ghr |
A |
G |
15: 3,357,506 (GRCm39) |
V254A |
probably benign |
Het |
Igkv8-28 |
A |
G |
6: 70,120,691 (GRCm39) |
V84A |
probably damaging |
Het |
Itgb7 |
T |
C |
15: 102,131,989 (GRCm39) |
D198G |
probably damaging |
Het |
Klra2 |
A |
G |
6: 131,197,070 (GRCm39) |
|
probably null |
Het |
Klrc2 |
A |
T |
6: 129,633,363 (GRCm39) |
Y230N |
probably damaging |
Het |
Lacc1 |
A |
G |
14: 77,267,024 (GRCm39) |
V413A |
probably damaging |
Het |
Muc16 |
T |
C |
9: 18,508,331 (GRCm39) |
N6355S |
probably benign |
Het |
Ncor1 |
AGCTGCTGCTGCTGCTGCTGCTGCTG |
AGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
11: 62,324,437 (GRCm39) |
|
probably benign |
Het |
Ncor1 |
CTG |
CTGGTG |
11: 62,324,448 (GRCm39) |
|
probably benign |
Het |
Ndn |
A |
G |
7: 61,998,903 (GRCm39) |
K250E |
possibly damaging |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nt5e |
A |
G |
9: 88,249,416 (GRCm39) |
E450G |
probably benign |
Het |
Or4d6 |
A |
T |
19: 12,086,313 (GRCm39) |
M199K |
possibly damaging |
Het |
Or5p75-ps1 |
T |
A |
7: 108,107,790 (GRCm39) |
*176K |
probably null |
Het |
Or8k16 |
G |
T |
2: 85,520,626 (GRCm39) |
M284I |
|
Het |
Palld |
A |
G |
8: 61,968,264 (GRCm39) |
S1343P |
unknown |
Het |
Pcdha8 |
T |
A |
18: 37,126,843 (GRCm39) |
S442T |
possibly damaging |
Het |
Pole2 |
T |
C |
12: 69,255,719 (GRCm39) |
I349V |
probably benign |
Het |
Ptprb |
C |
T |
10: 116,158,390 (GRCm39) |
T487M |
probably benign |
Het |
Ptprc |
C |
T |
1: 137,993,960 (GRCm39) |
D1020N |
probably damaging |
Het |
Relch |
C |
T |
1: 105,669,039 (GRCm39) |
T1023I |
probably damaging |
Het |
Rnf26rt |
C |
T |
6: 76,473,615 (GRCm39) |
E334K |
probably benign |
Het |
Rsf1 |
GCGGCGGCG |
GCGGCGGCGACGGCGGCG |
7: 97,229,120 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
T |
C |
13: 11,571,490 (GRCm39) |
N4916S |
possibly damaging |
Het |
Selp |
C |
T |
1: 163,957,674 (GRCm39) |
P268S |
probably damaging |
Het |
Sema7a |
T |
A |
9: 57,864,608 (GRCm39) |
C333S |
probably damaging |
Het |
Sh2b1 |
TGGGGACCAGCTCAGCCACGGGGACCAGCTC |
TGGGGACCAGCTCAGCCACGGGGACCAGCTCAGCCACGGGGACCAGCTC |
7: 126,066,742 (GRCm39) |
|
probably benign |
Het |
Sh2b1 |
CAGCCACGGGGACCAGCT |
CAGCCACGGGGACCAGCTAAGCCACGGGGACCAGCT |
7: 126,066,754 (GRCm39) |
|
probably null |
Het |
Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
Shisa5 |
G |
A |
9: 108,867,712 (GRCm39) |
|
probably benign |
Het |
Snx27 |
A |
G |
3: 94,489,723 (GRCm39) |
V45A |
possibly damaging |
Het |
Srcap |
T |
C |
7: 127,139,531 (GRCm39) |
V1284A |
probably damaging |
Het |
Ssrp1 |
A |
G |
2: 84,872,610 (GRCm39) |
D416G |
probably damaging |
Het |
Tcstv1b |
C |
T |
13: 120,634,061 (GRCm39) |
|
probably benign |
Het |
Tectb |
A |
G |
19: 55,181,093 (GRCm39) |
Y144C |
|
Het |
Thap12 |
G |
T |
7: 98,359,348 (GRCm39) |
V76F |
probably damaging |
Het |
Ticam2 |
G |
C |
18: 46,693,748 (GRCm39) |
P113R |
probably damaging |
Het |
Tsg101 |
A |
G |
7: 46,558,772 (GRCm39) |
Y80H |
probably benign |
Het |
Unc5cl |
T |
A |
17: 48,770,656 (GRCm39) |
M368K |
probably damaging |
Het |
Vmn1r159 |
T |
A |
7: 22,542,141 (GRCm39) |
D297V |
possibly damaging |
Het |
Vmn2r98 |
G |
T |
17: 19,287,517 (GRCm39) |
S450I |
probably benign |
Het |
Zbtb8b |
T |
C |
4: 129,326,319 (GRCm39) |
E282G |
probably benign |
Het |
Zfp831 |
T |
C |
2: 174,486,789 (GRCm39) |
V488A |
probably benign |
Het |
Zng1 |
T |
A |
19: 24,930,684 (GRCm39) |
M122L |
possibly damaging |
Het |
Zzef1 |
G |
A |
11: 72,807,251 (GRCm39) |
V2710I |
probably damaging |
Het |
|
Other mutations in Utp20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00530:Utp20
|
APN |
10 |
88,661,306 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL00858:Utp20
|
APN |
10 |
88,644,987 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL00858:Utp20
|
APN |
10 |
88,645,000 (GRCm39) |
missense |
probably benign |
|
IGL00946:Utp20
|
APN |
10 |
88,584,177 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01061:Utp20
|
APN |
10 |
88,606,566 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01399:Utp20
|
APN |
10 |
88,594,164 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01548:Utp20
|
APN |
10 |
88,600,643 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01587:Utp20
|
APN |
10 |
88,623,397 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01789:Utp20
|
APN |
10 |
88,634,141 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01819:Utp20
|
APN |
10 |
88,628,549 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02070:Utp20
|
APN |
10 |
88,657,739 (GRCm39) |
splice site |
probably benign |
|
IGL02231:Utp20
|
APN |
10 |
88,627,030 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02244:Utp20
|
APN |
10 |
88,651,818 (GRCm39) |
splice site |
probably benign |
|
IGL02367:Utp20
|
APN |
10 |
88,607,715 (GRCm39) |
unclassified |
probably benign |
|
IGL02553:Utp20
|
APN |
10 |
88,600,657 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02748:Utp20
|
APN |
10 |
88,653,157 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02831:Utp20
|
APN |
10 |
88,651,770 (GRCm39) |
missense |
probably benign |
|
IGL02986:Utp20
|
APN |
10 |
88,611,147 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02997:Utp20
|
APN |
10 |
88,649,896 (GRCm39) |
missense |
probably benign |
|
IGL03105:Utp20
|
APN |
10 |
88,626,958 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03251:Utp20
|
APN |
10 |
88,653,188 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03337:Utp20
|
APN |
10 |
88,590,428 (GRCm39) |
missense |
probably benign |
|
IGL03348:Utp20
|
APN |
10 |
88,594,179 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03381:Utp20
|
APN |
10 |
88,657,867 (GRCm39) |
missense |
probably damaging |
0.99 |
Bell
|
UTSW |
10 |
88,628,487 (GRCm39) |
missense |
probably benign |
0.29 |
elite
|
UTSW |
10 |
88,606,670 (GRCm39) |
missense |
probably benign |
|
Margin
|
UTSW |
10 |
88,604,541 (GRCm39) |
missense |
probably benign |
0.04 |
Percentile
|
UTSW |
10 |
88,611,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R0037:Utp20
|
UTSW |
10 |
88,634,266 (GRCm39) |
missense |
probably benign |
0.05 |
R0107:Utp20
|
UTSW |
10 |
88,614,253 (GRCm39) |
missense |
probably benign |
0.03 |
R0197:Utp20
|
UTSW |
10 |
88,613,378 (GRCm39) |
missense |
probably benign |
0.22 |
R0219:Utp20
|
UTSW |
10 |
88,600,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R0315:Utp20
|
UTSW |
10 |
88,643,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R0328:Utp20
|
UTSW |
10 |
88,602,969 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0329:Utp20
|
UTSW |
10 |
88,653,841 (GRCm39) |
missense |
probably benign |
0.00 |
R0330:Utp20
|
UTSW |
10 |
88,653,841 (GRCm39) |
missense |
probably benign |
0.00 |
R0395:Utp20
|
UTSW |
10 |
88,654,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R0399:Utp20
|
UTSW |
10 |
88,656,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Utp20
|
UTSW |
10 |
88,657,931 (GRCm39) |
missense |
probably benign |
0.00 |
R0456:Utp20
|
UTSW |
10 |
88,590,435 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0491:Utp20
|
UTSW |
10 |
88,596,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R0557:Utp20
|
UTSW |
10 |
88,584,173 (GRCm39) |
missense |
probably damaging |
0.99 |
R0600:Utp20
|
UTSW |
10 |
88,603,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Utp20
|
UTSW |
10 |
88,606,613 (GRCm39) |
missense |
probably benign |
0.14 |
R1076:Utp20
|
UTSW |
10 |
88,608,405 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1076:Utp20
|
UTSW |
10 |
88,608,321 (GRCm39) |
missense |
probably benign |
0.36 |
R1330:Utp20
|
UTSW |
10 |
88,637,051 (GRCm39) |
missense |
probably damaging |
0.96 |
R1440:Utp20
|
UTSW |
10 |
88,655,201 (GRCm39) |
missense |
probably benign |
0.19 |
R1529:Utp20
|
UTSW |
10 |
88,588,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R1554:Utp20
|
UTSW |
10 |
88,600,599 (GRCm39) |
nonsense |
probably null |
|
R1621:Utp20
|
UTSW |
10 |
88,598,733 (GRCm39) |
missense |
probably benign |
|
R1641:Utp20
|
UTSW |
10 |
88,593,834 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1709:Utp20
|
UTSW |
10 |
88,585,159 (GRCm39) |
missense |
probably benign |
0.29 |
R1734:Utp20
|
UTSW |
10 |
88,603,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R1755:Utp20
|
UTSW |
10 |
88,645,631 (GRCm39) |
missense |
probably benign |
0.01 |
R1775:Utp20
|
UTSW |
10 |
88,606,670 (GRCm39) |
missense |
probably benign |
|
R1866:Utp20
|
UTSW |
10 |
88,598,632 (GRCm39) |
nonsense |
probably null |
|
R1867:Utp20
|
UTSW |
10 |
88,585,305 (GRCm39) |
missense |
probably benign |
|
R1901:Utp20
|
UTSW |
10 |
88,588,888 (GRCm39) |
missense |
probably benign |
0.02 |
R1902:Utp20
|
UTSW |
10 |
88,588,888 (GRCm39) |
missense |
probably benign |
0.02 |
R1967:Utp20
|
UTSW |
10 |
88,652,841 (GRCm39) |
missense |
probably benign |
0.03 |
R2060:Utp20
|
UTSW |
10 |
88,610,657 (GRCm39) |
missense |
probably damaging |
0.98 |
R2102:Utp20
|
UTSW |
10 |
88,608,779 (GRCm39) |
missense |
probably damaging |
0.99 |
R2110:Utp20
|
UTSW |
10 |
88,603,313 (GRCm39) |
critical splice donor site |
probably null |
|
R2115:Utp20
|
UTSW |
10 |
88,621,865 (GRCm39) |
missense |
probably benign |
0.02 |
R2128:Utp20
|
UTSW |
10 |
88,649,917 (GRCm39) |
missense |
probably damaging |
0.99 |
R2129:Utp20
|
UTSW |
10 |
88,649,917 (GRCm39) |
missense |
probably damaging |
0.99 |
R2180:Utp20
|
UTSW |
10 |
88,656,801 (GRCm39) |
missense |
probably damaging |
0.98 |
R2280:Utp20
|
UTSW |
10 |
88,661,365 (GRCm39) |
splice site |
probably null |
|
R2435:Utp20
|
UTSW |
10 |
88,656,753 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2914:Utp20
|
UTSW |
10 |
88,590,337 (GRCm39) |
critical splice donor site |
probably null |
|
R3005:Utp20
|
UTSW |
10 |
88,613,317 (GRCm39) |
missense |
probably damaging |
0.97 |
R3546:Utp20
|
UTSW |
10 |
88,618,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R3547:Utp20
|
UTSW |
10 |
88,618,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R3622:Utp20
|
UTSW |
10 |
88,593,855 (GRCm39) |
unclassified |
probably benign |
|
R3737:Utp20
|
UTSW |
10 |
88,598,668 (GRCm39) |
missense |
probably benign |
0.00 |
R3738:Utp20
|
UTSW |
10 |
88,598,668 (GRCm39) |
missense |
probably benign |
0.00 |
R3841:Utp20
|
UTSW |
10 |
88,611,065 (GRCm39) |
unclassified |
probably benign |
|
R4034:Utp20
|
UTSW |
10 |
88,598,668 (GRCm39) |
missense |
probably benign |
0.00 |
R4035:Utp20
|
UTSW |
10 |
88,598,668 (GRCm39) |
missense |
probably benign |
0.00 |
R4157:Utp20
|
UTSW |
10 |
88,597,729 (GRCm39) |
missense |
probably benign |
|
R4243:Utp20
|
UTSW |
10 |
88,643,187 (GRCm39) |
critical splice donor site |
probably null |
|
R4295:Utp20
|
UTSW |
10 |
88,590,381 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4632:Utp20
|
UTSW |
10 |
88,614,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R4633:Utp20
|
UTSW |
10 |
88,588,814 (GRCm39) |
missense |
probably benign |
|
R4684:Utp20
|
UTSW |
10 |
88,643,307 (GRCm39) |
nonsense |
probably null |
|
R4731:Utp20
|
UTSW |
10 |
88,590,382 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4735:Utp20
|
UTSW |
10 |
88,652,780 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4772:Utp20
|
UTSW |
10 |
88,645,797 (GRCm39) |
missense |
probably benign |
0.09 |
R4912:Utp20
|
UTSW |
10 |
88,607,822 (GRCm39) |
missense |
probably benign |
0.01 |
R4974:Utp20
|
UTSW |
10 |
88,652,811 (GRCm39) |
missense |
probably benign |
0.08 |
R4991:Utp20
|
UTSW |
10 |
88,582,796 (GRCm39) |
missense |
probably benign |
0.09 |
R5004:Utp20
|
UTSW |
10 |
88,584,135 (GRCm39) |
missense |
probably damaging |
0.98 |
R5037:Utp20
|
UTSW |
10 |
88,611,192 (GRCm39) |
missense |
probably benign |
0.00 |
R5043:Utp20
|
UTSW |
10 |
88,634,608 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5108:Utp20
|
UTSW |
10 |
88,604,735 (GRCm39) |
missense |
probably benign |
0.00 |
R5138:Utp20
|
UTSW |
10 |
88,583,239 (GRCm39) |
missense |
probably damaging |
0.96 |
R5252:Utp20
|
UTSW |
10 |
88,586,532 (GRCm39) |
missense |
probably benign |
0.01 |
R5394:Utp20
|
UTSW |
10 |
88,608,777 (GRCm39) |
nonsense |
probably null |
|
R5470:Utp20
|
UTSW |
10 |
88,653,758 (GRCm39) |
missense |
probably benign |
0.14 |
R5558:Utp20
|
UTSW |
10 |
88,587,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R5678:Utp20
|
UTSW |
10 |
88,644,979 (GRCm39) |
missense |
probably benign |
0.00 |
R5822:Utp20
|
UTSW |
10 |
88,653,147 (GRCm39) |
missense |
probably benign |
0.00 |
R5866:Utp20
|
UTSW |
10 |
88,608,421 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5924:Utp20
|
UTSW |
10 |
88,651,784 (GRCm39) |
missense |
probably benign |
0.00 |
R6026:Utp20
|
UTSW |
10 |
88,604,541 (GRCm39) |
missense |
probably benign |
0.04 |
R6363:Utp20
|
UTSW |
10 |
88,592,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R6434:Utp20
|
UTSW |
10 |
88,608,395 (GRCm39) |
nonsense |
probably null |
|
R6477:Utp20
|
UTSW |
10 |
88,604,780 (GRCm39) |
missense |
probably benign |
0.05 |
R6480:Utp20
|
UTSW |
10 |
88,591,048 (GRCm39) |
critical splice donor site |
probably null |
|
R6989:Utp20
|
UTSW |
10 |
88,614,102 (GRCm39) |
missense |
probably benign |
0.00 |
R7033:Utp20
|
UTSW |
10 |
88,590,337 (GRCm39) |
critical splice donor site |
probably null |
|
R7192:Utp20
|
UTSW |
10 |
88,608,321 (GRCm39) |
missense |
probably benign |
0.09 |
R7236:Utp20
|
UTSW |
10 |
88,585,204 (GRCm39) |
missense |
probably benign |
0.28 |
R7260:Utp20
|
UTSW |
10 |
88,587,334 (GRCm39) |
missense |
probably benign |
0.39 |
R7296:Utp20
|
UTSW |
10 |
88,606,586 (GRCm39) |
missense |
probably benign |
0.21 |
R7317:Utp20
|
UTSW |
10 |
88,598,797 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7318:Utp20
|
UTSW |
10 |
88,649,811 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7330:Utp20
|
UTSW |
10 |
88,623,424 (GRCm39) |
frame shift |
probably null |
|
R7367:Utp20
|
UTSW |
10 |
88,631,305 (GRCm39) |
missense |
probably benign |
0.21 |
R7432:Utp20
|
UTSW |
10 |
88,634,260 (GRCm39) |
missense |
probably benign |
0.00 |
R7447:Utp20
|
UTSW |
10 |
88,608,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7473:Utp20
|
UTSW |
10 |
88,656,572 (GRCm39) |
splice site |
probably null |
|
R7520:Utp20
|
UTSW |
10 |
88,654,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R7530:Utp20
|
UTSW |
10 |
88,588,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R7539:Utp20
|
UTSW |
10 |
88,627,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R7651:Utp20
|
UTSW |
10 |
88,590,457 (GRCm39) |
missense |
probably benign |
0.41 |
R7728:Utp20
|
UTSW |
10 |
88,634,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R7831:Utp20
|
UTSW |
10 |
88,598,632 (GRCm39) |
nonsense |
probably null |
|
R7833:Utp20
|
UTSW |
10 |
88,636,998 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7909:Utp20
|
UTSW |
10 |
88,611,192 (GRCm39) |
missense |
probably benign |
|
R7956:Utp20
|
UTSW |
10 |
88,618,476 (GRCm39) |
missense |
probably benign |
0.23 |
R7999:Utp20
|
UTSW |
10 |
88,606,250 (GRCm39) |
missense |
probably benign |
|
R8080:Utp20
|
UTSW |
10 |
88,618,577 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8098:Utp20
|
UTSW |
10 |
88,588,810 (GRCm39) |
missense |
probably benign |
0.13 |
R8104:Utp20
|
UTSW |
10 |
88,593,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R8129:Utp20
|
UTSW |
10 |
88,628,487 (GRCm39) |
missense |
probably benign |
0.29 |
R8147:Utp20
|
UTSW |
10 |
88,594,306 (GRCm39) |
missense |
probably benign |
0.02 |
R8199:Utp20
|
UTSW |
10 |
88,634,337 (GRCm39) |
missense |
probably benign |
|
R8222:Utp20
|
UTSW |
10 |
88,614,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R8415:Utp20
|
UTSW |
10 |
88,662,466 (GRCm39) |
critical splice donor site |
probably null |
|
R8466:Utp20
|
UTSW |
10 |
88,654,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R8505:Utp20
|
UTSW |
10 |
88,653,870 (GRCm39) |
missense |
probably benign |
0.03 |
R8774:Utp20
|
UTSW |
10 |
88,588,763 (GRCm39) |
splice site |
probably benign |
|
R8802:Utp20
|
UTSW |
10 |
88,583,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R8923:Utp20
|
UTSW |
10 |
88,627,604 (GRCm39) |
nonsense |
probably null |
|
R8945:Utp20
|
UTSW |
10 |
88,628,532 (GRCm39) |
nonsense |
probably null |
|
R9065:Utp20
|
UTSW |
10 |
88,592,972 (GRCm39) |
missense |
probably benign |
0.32 |
R9092:Utp20
|
UTSW |
10 |
88,611,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R9092:Utp20
|
UTSW |
10 |
88,604,679 (GRCm39) |
missense |
probably benign |
|
R9094:Utp20
|
UTSW |
10 |
88,611,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R9095:Utp20
|
UTSW |
10 |
88,611,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R9096:Utp20
|
UTSW |
10 |
88,611,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R9229:Utp20
|
UTSW |
10 |
88,594,239 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9323:Utp20
|
UTSW |
10 |
88,583,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R9336:Utp20
|
UTSW |
10 |
88,649,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R9545:Utp20
|
UTSW |
10 |
88,618,511 (GRCm39) |
missense |
probably benign |
0.38 |
R9659:Utp20
|
UTSW |
10 |
88,653,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R9788:Utp20
|
UTSW |
10 |
88,653,171 (GRCm39) |
missense |
probably damaging |
1.00 |
RF005:Utp20
|
UTSW |
10 |
88,661,319 (GRCm39) |
missense |
probably damaging |
1.00 |
RF024:Utp20
|
UTSW |
10 |
88,661,319 (GRCm39) |
missense |
probably damaging |
1.00 |
|