Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arid2 |
A |
G |
15: 96,259,680 (GRCm39) |
D280G |
probably damaging |
Het |
Atosa |
A |
G |
9: 74,917,672 (GRCm39) |
D757G |
probably damaging |
Het |
Azi2 |
C |
T |
9: 117,878,390 (GRCm39) |
R77* |
probably null |
Het |
Chd8 |
T |
C |
14: 52,468,950 (GRCm39) |
D556G |
probably benign |
Het |
Cit |
T |
C |
5: 116,085,983 (GRCm39) |
M849T |
probably damaging |
Het |
Cit |
T |
C |
5: 116,143,899 (GRCm39) |
S1923P |
probably damaging |
Het |
Col17a1 |
T |
A |
19: 47,639,185 (GRCm39) |
H1120L |
probably benign |
Het |
Col6a5 |
G |
T |
9: 105,814,193 (GRCm39) |
H606Q |
unknown |
Het |
Dnajc2 |
A |
C |
5: 21,981,788 (GRCm39) |
H45Q |
probably damaging |
Het |
Dpp6 |
A |
G |
5: 27,914,457 (GRCm39) |
D514G |
possibly damaging |
Het |
Dync2h1 |
A |
G |
9: 7,129,062 (GRCm39) |
S1818P |
probably damaging |
Het |
Efemp1 |
A |
T |
11: 28,864,696 (GRCm39) |
Y250F |
possibly damaging |
Het |
Emc1 |
G |
A |
4: 139,088,257 (GRCm39) |
E342K |
possibly damaging |
Het |
Fam3c |
T |
C |
6: 22,329,592 (GRCm39) |
D45G |
probably benign |
Het |
Fchsd2 |
A |
C |
7: 100,847,740 (GRCm39) |
D210A |
possibly damaging |
Het |
Flg |
T |
A |
3: 93,186,722 (GRCm39) |
M58K |
probably damaging |
Het |
Gabra5 |
G |
A |
7: 57,138,698 (GRCm39) |
R117C |
probably damaging |
Het |
Gm6741 |
G |
A |
17: 91,544,309 (GRCm39) |
S24N |
probably benign |
Het |
Grin2a |
T |
C |
16: 9,462,107 (GRCm39) |
D675G |
possibly damaging |
Het |
Hectd4 |
T |
G |
5: 121,419,981 (GRCm39) |
V642G |
possibly damaging |
Het |
Herc6 |
C |
T |
6: 57,560,317 (GRCm39) |
T119M |
probably benign |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Hmgcs2 |
T |
C |
3: 98,206,530 (GRCm39) |
S371P |
probably damaging |
Het |
Idua |
C |
T |
5: 108,828,600 (GRCm39) |
A271V |
probably damaging |
Het |
Inpp5d |
T |
A |
1: 87,623,072 (GRCm39) |
C125* |
probably null |
Het |
Krt14 |
C |
T |
11: 100,098,044 (GRCm39) |
G80R |
unknown |
Het |
Lama5 |
T |
C |
2: 179,820,923 (GRCm39) |
Y3176C |
probably benign |
Het |
Lce1k |
C |
T |
3: 92,713,809 (GRCm39) |
C125Y |
unknown |
Het |
Lig4 |
A |
T |
8: 10,022,436 (GRCm39) |
L448Q |
probably damaging |
Het |
Macf1 |
C |
T |
4: 123,265,711 (GRCm39) |
A4821T |
probably damaging |
Het |
Meioc |
C |
T |
11: 102,566,184 (GRCm39) |
A600V |
probably benign |
Het |
Mepe |
T |
C |
5: 104,474,957 (GRCm39) |
S13P |
possibly damaging |
Het |
Mms22l |
A |
G |
4: 24,588,365 (GRCm39) |
Y999C |
probably damaging |
Het |
Ncbp3 |
T |
A |
11: 72,944,346 (GRCm39) |
M116K |
possibly damaging |
Het |
Ndufa10 |
A |
G |
1: 92,367,614 (GRCm39) |
Y339H |
probably damaging |
Het |
Nkx3-1 |
T |
C |
14: 69,428,266 (GRCm39) |
I38T |
probably damaging |
Het |
Nup155 |
A |
T |
15: 8,187,244 (GRCm39) |
H1391L |
probably damaging |
Het |
Or4k49 |
T |
A |
2: 111,495,168 (GRCm39) |
M199K |
possibly damaging |
Het |
Padi6 |
T |
G |
4: 140,456,279 (GRCm39) |
I572L |
possibly damaging |
Het |
Pdss2 |
A |
T |
10: 43,269,871 (GRCm39) |
N238I |
possibly damaging |
Het |
Pkd1l2 |
A |
G |
8: 117,746,272 (GRCm39) |
V1906A |
probably benign |
Het |
Pom121 |
T |
C |
5: 135,410,404 (GRCm39) |
|
probably benign |
Het |
Psmd9 |
T |
C |
5: 123,379,925 (GRCm39) |
F115L |
probably damaging |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Rai1 |
T |
C |
11: 60,076,415 (GRCm39) |
F160L |
probably damaging |
Het |
Rhbdl2 |
A |
T |
4: 123,720,665 (GRCm39) |
R234S |
probably damaging |
Het |
Rnase2a |
T |
A |
14: 51,493,245 (GRCm39) |
Y40F |
probably damaging |
Het |
Setd2 |
T |
C |
9: 110,378,201 (GRCm39) |
V672A |
possibly damaging |
Het |
Sgpp2 |
A |
G |
1: 78,393,857 (GRCm39) |
I287V |
probably benign |
Het |
Sh3pxd2a |
T |
C |
19: 47,255,703 (GRCm39) |
E1033G |
probably benign |
Het |
Slc5a9 |
G |
A |
4: 111,747,728 (GRCm39) |
T284I |
probably damaging |
Het |
Slfn9 |
A |
G |
11: 82,872,507 (GRCm39) |
L743P |
probably damaging |
Het |
Smchd1 |
T |
A |
17: 71,677,923 (GRCm39) |
N1473I |
probably benign |
Het |
Stx1b |
A |
T |
7: 127,414,575 (GRCm39) |
D16E |
probably benign |
Het |
Tectb |
T |
C |
19: 55,170,361 (GRCm39) |
F71L |
probably damaging |
Het |
Tmem220 |
T |
C |
11: 66,924,979 (GRCm39) |
I138T |
possibly damaging |
Het |
Tmtc4 |
T |
C |
14: 123,158,677 (GRCm39) |
N682S |
probably benign |
Het |
Ubn1 |
T |
G |
16: 4,882,487 (GRCm39) |
L316W |
probably damaging |
Het |
Vwa5a |
T |
C |
9: 38,647,357 (GRCm39) |
S579P |
probably damaging |
Het |
Xdh |
A |
G |
17: 74,228,300 (GRCm39) |
L367P |
possibly damaging |
Het |
Zfp280b |
T |
C |
10: 75,874,328 (GRCm39) |
L69S |
probably damaging |
Het |
Zfp990 |
A |
C |
4: 145,263,974 (GRCm39) |
Y324S |
possibly damaging |
Het |
|
Other mutations in Tnc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Tnc
|
APN |
4 |
63,935,061 (GRCm39) |
splice site |
probably benign |
|
IGL00531:Tnc
|
APN |
4 |
63,889,390 (GRCm39) |
splice site |
probably benign |
|
IGL00674:Tnc
|
APN |
4 |
63,883,844 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01015:Tnc
|
APN |
4 |
63,935,571 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01090:Tnc
|
APN |
4 |
63,918,317 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01310:Tnc
|
APN |
4 |
63,931,314 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01331:Tnc
|
APN |
4 |
63,901,112 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01393:Tnc
|
APN |
4 |
63,932,291 (GRCm39) |
splice site |
probably benign |
|
IGL01411:Tnc
|
APN |
4 |
63,918,959 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01472:Tnc
|
APN |
4 |
63,924,656 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01552:Tnc
|
APN |
4 |
63,888,645 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01661:Tnc
|
APN |
4 |
63,888,544 (GRCm39) |
splice site |
probably benign |
|
IGL01669:Tnc
|
APN |
4 |
63,918,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01912:Tnc
|
APN |
4 |
63,926,977 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02028:Tnc
|
APN |
4 |
63,884,909 (GRCm39) |
splice site |
probably benign |
|
IGL02100:Tnc
|
APN |
4 |
63,918,398 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02549:Tnc
|
APN |
4 |
63,933,309 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02642:Tnc
|
APN |
4 |
63,883,816 (GRCm39) |
splice site |
probably benign |
|
IGL02712:Tnc
|
APN |
4 |
63,893,493 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02876:Tnc
|
APN |
4 |
63,933,338 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02886:Tnc
|
APN |
4 |
63,918,344 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02972:Tnc
|
APN |
4 |
63,894,715 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03073:Tnc
|
APN |
4 |
63,889,461 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL03116:Tnc
|
APN |
4 |
63,932,270 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03181:Tnc
|
APN |
4 |
63,885,543 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03358:Tnc
|
APN |
4 |
63,935,852 (GRCm39) |
nonsense |
probably null |
|
tancredo
|
UTSW |
4 |
63,911,534 (GRCm39) |
nonsense |
probably null |
|
BB009:Tnc
|
UTSW |
4 |
63,926,857 (GRCm39) |
missense |
probably benign |
|
BB019:Tnc
|
UTSW |
4 |
63,926,857 (GRCm39) |
missense |
probably benign |
|
P0020:Tnc
|
UTSW |
4 |
63,927,094 (GRCm39) |
missense |
possibly damaging |
0.63 |
PIT4377001:Tnc
|
UTSW |
4 |
63,935,973 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4403001:Tnc
|
UTSW |
4 |
63,882,904 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4468001:Tnc
|
UTSW |
4 |
63,882,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R0243:Tnc
|
UTSW |
4 |
63,888,657 (GRCm39) |
missense |
probably damaging |
0.98 |
R0362:Tnc
|
UTSW |
4 |
63,935,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0410:Tnc
|
UTSW |
4 |
63,925,931 (GRCm39) |
missense |
probably benign |
0.00 |
R0420:Tnc
|
UTSW |
4 |
63,918,396 (GRCm39) |
missense |
probably benign |
0.00 |
R0540:Tnc
|
UTSW |
4 |
63,938,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R0650:Tnc
|
UTSW |
4 |
63,926,971 (GRCm39) |
missense |
probably benign |
0.00 |
R1019:Tnc
|
UTSW |
4 |
63,880,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R1102:Tnc
|
UTSW |
4 |
63,938,705 (GRCm39) |
missense |
probably benign |
0.05 |
R1126:Tnc
|
UTSW |
4 |
63,936,357 (GRCm39) |
missense |
probably damaging |
0.99 |
R1141:Tnc
|
UTSW |
4 |
63,932,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R1142:Tnc
|
UTSW |
4 |
63,932,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R1307:Tnc
|
UTSW |
4 |
63,927,096 (GRCm39) |
missense |
probably damaging |
0.98 |
R1322:Tnc
|
UTSW |
4 |
63,932,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R1414:Tnc
|
UTSW |
4 |
63,883,932 (GRCm39) |
splice site |
probably benign |
|
R1470:Tnc
|
UTSW |
4 |
63,884,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Tnc
|
UTSW |
4 |
63,884,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R1499:Tnc
|
UTSW |
4 |
63,882,991 (GRCm39) |
missense |
probably benign |
0.15 |
R1506:Tnc
|
UTSW |
4 |
63,925,921 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1597:Tnc
|
UTSW |
4 |
63,924,621 (GRCm39) |
missense |
probably benign |
|
R1750:Tnc
|
UTSW |
4 |
63,890,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R1765:Tnc
|
UTSW |
4 |
63,932,231 (GRCm39) |
missense |
probably damaging |
1.00 |
R1783:Tnc
|
UTSW |
4 |
63,936,333 (GRCm39) |
missense |
probably damaging |
0.98 |
R1808:Tnc
|
UTSW |
4 |
63,918,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Tnc
|
UTSW |
4 |
63,918,299 (GRCm39) |
missense |
probably benign |
0.00 |
R1932:Tnc
|
UTSW |
4 |
63,911,262 (GRCm39) |
critical splice donor site |
probably null |
|
R1941:Tnc
|
UTSW |
4 |
63,933,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Tnc
|
UTSW |
4 |
63,902,867 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2075:Tnc
|
UTSW |
4 |
63,913,903 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2327:Tnc
|
UTSW |
4 |
63,893,475 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2444:Tnc
|
UTSW |
4 |
63,933,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R2982:Tnc
|
UTSW |
4 |
63,938,756 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3874:Tnc
|
UTSW |
4 |
63,926,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R4110:Tnc
|
UTSW |
4 |
63,933,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R4360:Tnc
|
UTSW |
4 |
63,935,161 (GRCm39) |
missense |
probably benign |
0.35 |
R4371:Tnc
|
UTSW |
4 |
63,888,588 (GRCm39) |
missense |
probably damaging |
1.00 |
R4434:Tnc
|
UTSW |
4 |
63,926,066 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4438:Tnc
|
UTSW |
4 |
63,926,066 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4570:Tnc
|
UTSW |
4 |
63,913,909 (GRCm39) |
missense |
probably damaging |
0.99 |
R4595:Tnc
|
UTSW |
4 |
63,913,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R4749:Tnc
|
UTSW |
4 |
63,913,876 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4756:Tnc
|
UTSW |
4 |
63,885,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R4824:Tnc
|
UTSW |
4 |
63,935,857 (GRCm39) |
nonsense |
probably null |
|
R4957:Tnc
|
UTSW |
4 |
63,894,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R4977:Tnc
|
UTSW |
4 |
63,924,485 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5001:Tnc
|
UTSW |
4 |
63,918,299 (GRCm39) |
missense |
probably benign |
0.16 |
R5001:Tnc
|
UTSW |
4 |
63,902,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R5015:Tnc
|
UTSW |
4 |
63,924,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R5049:Tnc
|
UTSW |
4 |
63,936,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R5066:Tnc
|
UTSW |
4 |
63,893,466 (GRCm39) |
missense |
probably damaging |
0.96 |
R5073:Tnc
|
UTSW |
4 |
63,938,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R5116:Tnc
|
UTSW |
4 |
63,885,452 (GRCm39) |
critical splice donor site |
probably null |
|
R5195:Tnc
|
UTSW |
4 |
63,885,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5200:Tnc
|
UTSW |
4 |
63,889,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R5221:Tnc
|
UTSW |
4 |
63,911,534 (GRCm39) |
nonsense |
probably null |
|
R5237:Tnc
|
UTSW |
4 |
63,880,333 (GRCm39) |
missense |
probably damaging |
1.00 |
R5265:Tnc
|
UTSW |
4 |
63,911,443 (GRCm39) |
missense |
probably benign |
0.00 |
R5275:Tnc
|
UTSW |
4 |
63,882,967 (GRCm39) |
nonsense |
probably null |
|
R5346:Tnc
|
UTSW |
4 |
63,926,892 (GRCm39) |
missense |
probably benign |
|
R5409:Tnc
|
UTSW |
4 |
63,925,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R5409:Tnc
|
UTSW |
4 |
63,884,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R5469:Tnc
|
UTSW |
4 |
63,932,162 (GRCm39) |
splice site |
probably null |
|
R5518:Tnc
|
UTSW |
4 |
63,935,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Tnc
|
UTSW |
4 |
63,926,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R5588:Tnc
|
UTSW |
4 |
63,924,659 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5686:Tnc
|
UTSW |
4 |
63,925,967 (GRCm39) |
splice site |
probably null |
|
R5686:Tnc
|
UTSW |
4 |
63,927,032 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5837:Tnc
|
UTSW |
4 |
63,931,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R5976:Tnc
|
UTSW |
4 |
63,936,403 (GRCm39) |
missense |
probably benign |
0.17 |
R6156:Tnc
|
UTSW |
4 |
63,888,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R6182:Tnc
|
UTSW |
4 |
63,927,033 (GRCm39) |
missense |
probably damaging |
0.99 |
R6360:Tnc
|
UTSW |
4 |
63,918,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R6416:Tnc
|
UTSW |
4 |
63,926,053 (GRCm39) |
missense |
probably benign |
0.05 |
R6778:Tnc
|
UTSW |
4 |
63,913,835 (GRCm39) |
missense |
probably benign |
0.12 |
R6798:Tnc
|
UTSW |
4 |
63,883,841 (GRCm39) |
missense |
probably benign |
0.02 |
R6799:Tnc
|
UTSW |
4 |
63,883,841 (GRCm39) |
missense |
probably benign |
0.02 |
R6943:Tnc
|
UTSW |
4 |
63,900,982 (GRCm39) |
missense |
probably damaging |
0.97 |
R7027:Tnc
|
UTSW |
4 |
63,902,826 (GRCm39) |
missense |
probably benign |
0.02 |
R7183:Tnc
|
UTSW |
4 |
63,931,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R7204:Tnc
|
UTSW |
4 |
63,889,392 (GRCm39) |
splice site |
probably null |
|
R7317:Tnc
|
UTSW |
4 |
63,890,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R7323:Tnc
|
UTSW |
4 |
63,889,469 (GRCm39) |
missense |
probably damaging |
0.96 |
R7327:Tnc
|
UTSW |
4 |
63,882,999 (GRCm39) |
splice site |
probably null |
|
R7382:Tnc
|
UTSW |
4 |
63,932,280 (GRCm39) |
nonsense |
probably null |
|
R7399:Tnc
|
UTSW |
4 |
63,938,894 (GRCm39) |
start gained |
probably benign |
|
R7479:Tnc
|
UTSW |
4 |
63,935,865 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7585:Tnc
|
UTSW |
4 |
63,938,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R7932:Tnc
|
UTSW |
4 |
63,926,857 (GRCm39) |
missense |
probably benign |
|
R7947:Tnc
|
UTSW |
4 |
63,935,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R7974:Tnc
|
UTSW |
4 |
63,918,961 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7991:Tnc
|
UTSW |
4 |
63,926,983 (GRCm39) |
missense |
probably benign |
0.42 |
R8004:Tnc
|
UTSW |
4 |
63,902,894 (GRCm39) |
missense |
probably benign |
0.04 |
R8080:Tnc
|
UTSW |
4 |
63,894,706 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8109:Tnc
|
UTSW |
4 |
63,927,000 (GRCm39) |
missense |
probably benign |
0.11 |
R8145:Tnc
|
UTSW |
4 |
63,935,716 (GRCm39) |
missense |
probably benign |
|
R8340:Tnc
|
UTSW |
4 |
63,926,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R8360:Tnc
|
UTSW |
4 |
63,885,511 (GRCm39) |
missense |
probably benign |
0.00 |
R8671:Tnc
|
UTSW |
4 |
63,935,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R8691:Tnc
|
UTSW |
4 |
63,880,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R8759:Tnc
|
UTSW |
4 |
63,924,501 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8864:Tnc
|
UTSW |
4 |
63,911,296 (GRCm39) |
missense |
probably damaging |
0.98 |
R8927:Tnc
|
UTSW |
4 |
63,925,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R8928:Tnc
|
UTSW |
4 |
63,925,595 (GRCm39) |
missense |
probably damaging |
1.00 |
R8949:Tnc
|
UTSW |
4 |
63,927,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R8956:Tnc
|
UTSW |
4 |
63,918,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R9016:Tnc
|
UTSW |
4 |
63,935,331 (GRCm39) |
missense |
probably benign |
0.23 |
R9049:Tnc
|
UTSW |
4 |
63,918,247 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9097:Tnc
|
UTSW |
4 |
63,888,622 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9114:Tnc
|
UTSW |
4 |
63,890,973 (GRCm39) |
missense |
probably benign |
0.03 |
R9151:Tnc
|
UTSW |
4 |
63,938,686 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9488:Tnc
|
UTSW |
4 |
63,913,942 (GRCm39) |
missense |
probably damaging |
0.99 |
R9537:Tnc
|
UTSW |
4 |
63,884,821 (GRCm39) |
missense |
probably damaging |
0.99 |
R9666:Tnc
|
UTSW |
4 |
63,926,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R9700:Tnc
|
UTSW |
4 |
63,933,186 (GRCm39) |
missense |
probably damaging |
0.99 |
R9703:Tnc
|
UTSW |
4 |
63,889,412 (GRCm39) |
missense |
probably benign |
0.00 |
R9771:Tnc
|
UTSW |
4 |
63,925,600 (GRCm39) |
missense |
probably damaging |
1.00 |
S24628:Tnc
|
UTSW |
4 |
63,936,249 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tnc
|
UTSW |
4 |
63,925,663 (GRCm39) |
nonsense |
probably null |
|
Z1177:Tnc
|
UTSW |
4 |
63,878,781 (GRCm39) |
critical splice acceptor site |
probably null |
|
|