Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aars1 |
T |
G |
8: 111,768,206 (GRCm39) |
Y192* |
probably null |
Het |
Abcc6 |
T |
C |
7: 45,634,677 (GRCm39) |
Y1100C |
probably damaging |
Het |
Adamtsl2 |
T |
C |
2: 26,974,092 (GRCm39) |
W132R |
probably damaging |
Het |
Adgra2 |
T |
A |
8: 27,604,416 (GRCm39) |
V497E |
probably damaging |
Het |
Adtrp |
T |
G |
13: 41,981,813 (GRCm39) |
|
probably benign |
Het |
Alg9 |
T |
A |
9: 50,700,833 (GRCm39) |
L201Q |
possibly damaging |
Het |
Ap4e1 |
T |
A |
2: 126,856,121 (GRCm39) |
I84K |
probably damaging |
Het |
Atrnl1 |
T |
C |
19: 57,638,725 (GRCm39) |
S288P |
probably damaging |
Het |
Bltp1 |
T |
A |
3: 36,949,452 (GRCm39) |
L366Q |
possibly damaging |
Het |
Cacna1a |
A |
G |
8: 85,306,846 (GRCm39) |
D1367G |
probably damaging |
Het |
Card19 |
C |
T |
13: 49,358,727 (GRCm39) |
R82Q |
probably damaging |
Het |
Cep128 |
T |
C |
12: 91,292,372 (GRCm39) |
I226V |
possibly damaging |
Het |
Ces1f |
A |
C |
8: 93,994,633 (GRCm39) |
D259E |
probably benign |
Het |
Ckap5 |
T |
A |
2: 91,416,611 (GRCm39) |
M1072K |
probably benign |
Het |
Dcpp2 |
T |
A |
17: 24,119,468 (GRCm39) |
V94D |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,337,474 (GRCm39) |
D3209G |
possibly damaging |
Het |
Dsg1c |
A |
G |
18: 20,416,255 (GRCm39) |
T719A |
probably damaging |
Het |
Dsp |
G |
A |
13: 38,375,716 (GRCm39) |
W1167* |
probably null |
Het |
Eml5 |
T |
C |
12: 98,758,305 (GRCm39) |
I1874V |
probably benign |
Het |
Epg5 |
A |
G |
18: 78,003,926 (GRCm39) |
T645A |
probably damaging |
Het |
F2rl2 |
T |
C |
13: 95,837,621 (GRCm39) |
L222S |
probably damaging |
Het |
Fam114a1 |
T |
A |
5: 65,191,731 (GRCm39) |
C495S |
probably damaging |
Het |
Fbn1 |
A |
T |
2: 125,163,537 (GRCm39) |
D2106E |
probably benign |
Het |
Fgf14 |
T |
A |
14: 124,913,936 (GRCm39) |
N65I |
probably benign |
Het |
Fip1l1 |
T |
C |
5: 74,755,763 (GRCm39) |
Y497H |
probably damaging |
Het |
Fn1 |
A |
C |
1: 71,625,404 (GRCm39) |
D2376E |
probably damaging |
Het |
Foxd2 |
T |
C |
4: 114,764,662 (GRCm39) |
T453A |
possibly damaging |
Het |
Galnt1 |
G |
T |
18: 24,404,647 (GRCm39) |
W328L |
probably damaging |
Het |
Gapt |
A |
G |
13: 110,490,372 (GRCm39) |
V97A |
possibly damaging |
Het |
Gatad1 |
A |
G |
5: 3,693,707 (GRCm39) |
V154A |
possibly damaging |
Het |
Gdf15 |
A |
G |
8: 71,084,202 (GRCm39) |
F21L |
probably benign |
Het |
Igdcc4 |
T |
C |
9: 65,029,182 (GRCm39) |
F273S |
possibly damaging |
Het |
Invs |
A |
T |
4: 48,421,725 (GRCm39) |
R786W |
possibly damaging |
Het |
Itfg1 |
T |
G |
8: 86,507,152 (GRCm39) |
E236A |
probably benign |
Het |
Jak3 |
A |
T |
8: 72,137,194 (GRCm39) |
I752F |
probably damaging |
Het |
Kcnip3 |
C |
A |
2: 127,306,985 (GRCm39) |
G144W |
probably damaging |
Het |
Kctd19 |
T |
C |
8: 106,109,598 (GRCm39) |
H925R |
probably benign |
Het |
Kdr |
C |
T |
5: 76,107,511 (GRCm39) |
A1011T |
probably damaging |
Het |
Kif13b |
C |
A |
14: 65,019,826 (GRCm39) |
H1398Q |
probably benign |
Het |
Lrp4 |
A |
T |
2: 91,307,864 (GRCm39) |
|
probably null |
Het |
Lrtm2 |
T |
C |
6: 119,297,846 (GRCm39) |
D65G |
probably benign |
Het |
Lyz1 |
A |
G |
10: 117,128,715 (GRCm39) |
L10P |
probably damaging |
Het |
Metap2 |
A |
T |
10: 93,706,046 (GRCm39) |
N245K |
probably damaging |
Het |
Mms19 |
T |
C |
19: 41,943,270 (GRCm39) |
D297G |
possibly damaging |
Het |
Mocs3 |
A |
G |
2: 168,073,573 (GRCm39) |
D340G |
possibly damaging |
Het |
Mtfr1l |
A |
G |
4: 134,256,436 (GRCm39) |
L243P |
probably damaging |
Het |
Mtss1 |
A |
G |
15: 58,842,897 (GRCm39) |
I105T |
probably damaging |
Het |
Myo18a |
T |
C |
11: 77,748,571 (GRCm39) |
S1967P |
probably damaging |
Het |
Ncor2 |
T |
C |
5: 125,100,585 (GRCm39) |
N2248S |
possibly damaging |
Het |
Nfatc2 |
T |
C |
2: 168,432,008 (GRCm39) |
D35G |
possibly damaging |
Het |
Or10a3n |
A |
G |
7: 108,492,948 (GRCm39) |
L222P |
probably damaging |
Het |
Otof |
T |
C |
5: 30,529,256 (GRCm39) |
S1753G |
probably damaging |
Het |
Otog |
G |
A |
7: 45,939,179 (GRCm39) |
V2070I |
probably benign |
Het |
Piezo2 |
A |
G |
18: 63,219,824 (GRCm39) |
V961A |
probably damaging |
Het |
Pofut1 |
C |
T |
2: 153,103,158 (GRCm39) |
S169L |
probably benign |
Het |
Ppp1r10 |
T |
A |
17: 36,240,335 (GRCm39) |
S542T |
possibly damaging |
Het |
Prpf8 |
T |
C |
11: 75,381,156 (GRCm39) |
Y219H |
possibly damaging |
Het |
Ptges3l |
T |
C |
11: 101,312,731 (GRCm39) |
D113G |
possibly damaging |
Het |
Pycr3 |
G |
A |
15: 75,790,647 (GRCm39) |
L71F |
probably benign |
Het |
Ramp3 |
A |
G |
11: 6,624,867 (GRCm39) |
K54E |
possibly damaging |
Het |
Rbpms |
C |
A |
8: 34,294,100 (GRCm39) |
Q214H |
possibly damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Robo4 |
C |
A |
9: 37,319,348 (GRCm39) |
D565E |
probably damaging |
Het |
S100a1 |
C |
T |
3: 90,418,641 (GRCm39) |
V58I |
probably benign |
Het |
Setx |
T |
A |
2: 29,070,104 (GRCm39) |
D2636E |
probably benign |
Het |
Sun2 |
A |
T |
15: 79,612,669 (GRCm39) |
V417E |
probably damaging |
Het |
Tbccd1 |
T |
C |
16: 22,660,519 (GRCm39) |
N99S |
probably benign |
Het |
Tex15 |
A |
G |
8: 34,064,893 (GRCm39) |
D1441G |
probably benign |
Het |
Tmc2 |
T |
A |
2: 130,089,896 (GRCm39) |
M627K |
probably damaging |
Het |
Trim32 |
A |
G |
4: 65,532,628 (GRCm39) |
Y395C |
probably benign |
Het |
Trpm2 |
A |
G |
10: 77,759,398 (GRCm39) |
Y1129H |
probably damaging |
Het |
Trpm8 |
A |
T |
1: 88,275,813 (GRCm39) |
R470S |
probably damaging |
Het |
Tsg101 |
G |
T |
7: 46,539,372 (GRCm39) |
D389E |
probably benign |
Het |
Ubn1 |
T |
C |
16: 4,882,406 (GRCm39) |
L46P |
probably damaging |
Het |
Ubr5 |
T |
C |
15: 37,997,419 (GRCm39) |
I1745V |
possibly damaging |
Het |
Usp20 |
T |
C |
2: 30,901,797 (GRCm39) |
Y521H |
probably benign |
Het |
Vmn1r159 |
A |
T |
7: 22,543,019 (GRCm39) |
H4Q |
probably null |
Het |
Vmn2r27 |
T |
A |
6: 124,177,491 (GRCm39) |
E504D |
probably benign |
Het |
Wdr72 |
A |
T |
9: 74,086,867 (GRCm39) |
I612F |
probably benign |
Het |
Zbtb8a |
T |
C |
4: 129,251,520 (GRCm39) |
H317R |
possibly damaging |
Het |
Zfp507 |
T |
C |
7: 35,494,315 (GRCm39) |
S243G |
probably damaging |
Het |
Zfp764 |
A |
G |
7: 127,005,419 (GRCm39) |
W73R |
probably damaging |
Het |
Zmym4 |
A |
T |
4: 126,819,632 (GRCm39) |
D90E |
probably damaging |
Het |
|
Other mutations in Nup210l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00780:Nup210l
|
APN |
3 |
90,098,156 (GRCm39) |
splice site |
probably benign |
|
IGL00813:Nup210l
|
APN |
3 |
90,039,725 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01375:Nup210l
|
APN |
3 |
90,067,200 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01731:Nup210l
|
APN |
3 |
90,061,873 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01786:Nup210l
|
APN |
3 |
90,030,083 (GRCm39) |
nonsense |
probably null |
|
IGL01958:Nup210l
|
APN |
3 |
90,111,231 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02094:Nup210l
|
APN |
3 |
90,087,520 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02120:Nup210l
|
APN |
3 |
90,044,169 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02313:Nup210l
|
APN |
3 |
90,030,099 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02336:Nup210l
|
APN |
3 |
90,088,859 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02348:Nup210l
|
APN |
3 |
90,011,471 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL02372:Nup210l
|
APN |
3 |
90,109,278 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02557:Nup210l
|
APN |
3 |
90,031,537 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02559:Nup210l
|
APN |
3 |
90,067,260 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02738:Nup210l
|
APN |
3 |
90,044,157 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03231:Nup210l
|
APN |
3 |
90,096,852 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03257:Nup210l
|
APN |
3 |
90,087,455 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03388:Nup210l
|
APN |
3 |
90,077,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03134:Nup210l
|
UTSW |
3 |
90,098,194 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0003:Nup210l
|
UTSW |
3 |
90,027,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R0040:Nup210l
|
UTSW |
3 |
90,089,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R0083:Nup210l
|
UTSW |
3 |
90,096,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R0090:Nup210l
|
UTSW |
3 |
90,119,086 (GRCm39) |
missense |
probably benign |
0.00 |
R0108:Nup210l
|
UTSW |
3 |
90,096,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R0142:Nup210l
|
UTSW |
3 |
90,079,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R0306:Nup210l
|
UTSW |
3 |
90,114,675 (GRCm39) |
missense |
probably benign |
0.13 |
R0332:Nup210l
|
UTSW |
3 |
90,039,616 (GRCm39) |
splice site |
probably benign |
|
R0346:Nup210l
|
UTSW |
3 |
90,096,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R0463:Nup210l
|
UTSW |
3 |
90,087,518 (GRCm39) |
missense |
probably null |
1.00 |
R0622:Nup210l
|
UTSW |
3 |
90,075,047 (GRCm39) |
missense |
probably damaging |
0.98 |
R0765:Nup210l
|
UTSW |
3 |
90,027,184 (GRCm39) |
missense |
probably damaging |
0.99 |
R0990:Nup210l
|
UTSW |
3 |
90,119,232 (GRCm39) |
missense |
probably benign |
0.00 |
R1014:Nup210l
|
UTSW |
3 |
90,077,355 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1036:Nup210l
|
UTSW |
3 |
90,100,247 (GRCm39) |
splice site |
probably benign |
|
R1177:Nup210l
|
UTSW |
3 |
90,109,310 (GRCm39) |
missense |
probably benign |
0.11 |
R1188:Nup210l
|
UTSW |
3 |
90,105,486 (GRCm39) |
missense |
probably benign |
0.16 |
R1457:Nup210l
|
UTSW |
3 |
90,098,279 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1471:Nup210l
|
UTSW |
3 |
90,077,869 (GRCm39) |
missense |
probably benign |
|
R1627:Nup210l
|
UTSW |
3 |
90,051,476 (GRCm39) |
missense |
probably benign |
0.15 |
R1778:Nup210l
|
UTSW |
3 |
90,096,793 (GRCm39) |
missense |
probably damaging |
0.99 |
R1827:Nup210l
|
UTSW |
3 |
90,061,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R1843:Nup210l
|
UTSW |
3 |
90,079,393 (GRCm39) |
missense |
probably damaging |
0.96 |
R1858:Nup210l
|
UTSW |
3 |
90,061,806 (GRCm39) |
missense |
probably damaging |
0.97 |
R1942:Nup210l
|
UTSW |
3 |
90,058,544 (GRCm39) |
missense |
probably benign |
0.01 |
R2015:Nup210l
|
UTSW |
3 |
90,092,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R2113:Nup210l
|
UTSW |
3 |
90,098,281 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2944:Nup210l
|
UTSW |
3 |
90,088,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R3736:Nup210l
|
UTSW |
3 |
90,027,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R3740:Nup210l
|
UTSW |
3 |
90,114,701 (GRCm39) |
missense |
probably benign |
0.08 |
R3741:Nup210l
|
UTSW |
3 |
90,114,701 (GRCm39) |
missense |
probably benign |
0.08 |
R3742:Nup210l
|
UTSW |
3 |
90,114,701 (GRCm39) |
missense |
probably benign |
0.08 |
R3771:Nup210l
|
UTSW |
3 |
90,027,201 (GRCm39) |
nonsense |
probably null |
|
R3773:Nup210l
|
UTSW |
3 |
90,027,201 (GRCm39) |
nonsense |
probably null |
|
R3879:Nup210l
|
UTSW |
3 |
90,092,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R3882:Nup210l
|
UTSW |
3 |
90,031,517 (GRCm39) |
missense |
probably benign |
0.19 |
R3953:Nup210l
|
UTSW |
3 |
90,100,361 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3954:Nup210l
|
UTSW |
3 |
90,100,361 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3955:Nup210l
|
UTSW |
3 |
90,100,361 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3956:Nup210l
|
UTSW |
3 |
90,100,361 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4200:Nup210l
|
UTSW |
3 |
90,027,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R4290:Nup210l
|
UTSW |
3 |
90,114,633 (GRCm39) |
missense |
probably benign |
0.00 |
R4328:Nup210l
|
UTSW |
3 |
90,083,142 (GRCm39) |
splice site |
probably null |
|
R4629:Nup210l
|
UTSW |
3 |
90,098,181 (GRCm39) |
nonsense |
probably null |
|
R4629:Nup210l
|
UTSW |
3 |
90,075,182 (GRCm39) |
missense |
probably benign |
0.21 |
R4897:Nup210l
|
UTSW |
3 |
90,100,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R4906:Nup210l
|
UTSW |
3 |
90,077,337 (GRCm39) |
missense |
probably benign |
0.06 |
R4966:Nup210l
|
UTSW |
3 |
90,014,208 (GRCm39) |
missense |
probably benign |
0.00 |
R5004:Nup210l
|
UTSW |
3 |
90,087,472 (GRCm39) |
nonsense |
probably null |
|
R5237:Nup210l
|
UTSW |
3 |
90,087,505 (GRCm39) |
missense |
probably benign |
0.00 |
R5499:Nup210l
|
UTSW |
3 |
90,081,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R5522:Nup210l
|
UTSW |
3 |
90,061,972 (GRCm39) |
missense |
probably benign |
0.10 |
R5627:Nup210l
|
UTSW |
3 |
90,051,557 (GRCm39) |
missense |
probably damaging |
0.97 |
R5678:Nup210l
|
UTSW |
3 |
90,098,266 (GRCm39) |
missense |
probably damaging |
0.99 |
R5726:Nup210l
|
UTSW |
3 |
90,036,514 (GRCm39) |
splice site |
probably null |
|
R5792:Nup210l
|
UTSW |
3 |
90,107,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R6129:Nup210l
|
UTSW |
3 |
90,011,483 (GRCm39) |
missense |
probably benign |
0.00 |
R6272:Nup210l
|
UTSW |
3 |
90,077,331 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6290:Nup210l
|
UTSW |
3 |
90,027,216 (GRCm39) |
nonsense |
probably null |
|
R6293:Nup210l
|
UTSW |
3 |
90,022,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R6446:Nup210l
|
UTSW |
3 |
90,079,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R6698:Nup210l
|
UTSW |
3 |
90,089,815 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6855:Nup210l
|
UTSW |
3 |
90,044,231 (GRCm39) |
missense |
probably benign |
0.01 |
R6895:Nup210l
|
UTSW |
3 |
90,067,231 (GRCm39) |
missense |
probably damaging |
0.97 |
R6899:Nup210l
|
UTSW |
3 |
90,075,204 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6978:Nup210l
|
UTSW |
3 |
90,061,873 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6980:Nup210l
|
UTSW |
3 |
90,027,234 (GRCm39) |
missense |
probably benign |
0.04 |
R7038:Nup210l
|
UTSW |
3 |
90,067,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R7273:Nup210l
|
UTSW |
3 |
90,025,854 (GRCm39) |
missense |
probably benign |
0.04 |
R7450:Nup210l
|
UTSW |
3 |
90,022,495 (GRCm39) |
critical splice donor site |
probably null |
|
R7514:Nup210l
|
UTSW |
3 |
90,117,766 (GRCm39) |
critical splice donor site |
probably null |
|
R7658:Nup210l
|
UTSW |
3 |
90,119,300 (GRCm39) |
missense |
probably benign |
0.43 |
R7735:Nup210l
|
UTSW |
3 |
90,092,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R7772:Nup210l
|
UTSW |
3 |
90,067,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R7800:Nup210l
|
UTSW |
3 |
90,041,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R7840:Nup210l
|
UTSW |
3 |
90,030,036 (GRCm39) |
missense |
probably benign |
0.08 |
R7847:Nup210l
|
UTSW |
3 |
90,058,430 (GRCm39) |
missense |
probably benign |
|
R7848:Nup210l
|
UTSW |
3 |
90,111,212 (GRCm39) |
missense |
probably benign |
0.01 |
R8084:Nup210l
|
UTSW |
3 |
90,043,365 (GRCm39) |
missense |
probably benign |
0.15 |
R8121:Nup210l
|
UTSW |
3 |
90,022,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R8421:Nup210l
|
UTSW |
3 |
90,111,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R8458:Nup210l
|
UTSW |
3 |
90,092,874 (GRCm39) |
missense |
probably null |
1.00 |
R8701:Nup210l
|
UTSW |
3 |
90,030,121 (GRCm39) |
missense |
probably benign |
0.41 |
R8720:Nup210l
|
UTSW |
3 |
90,117,681 (GRCm39) |
missense |
probably benign |
0.00 |
R8770:Nup210l
|
UTSW |
3 |
90,025,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R8896:Nup210l
|
UTSW |
3 |
90,025,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R9033:Nup210l
|
UTSW |
3 |
90,105,396 (GRCm39) |
missense |
probably benign |
|
R9371:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9373:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9381:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9426:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9427:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9501:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9523:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9574:Nup210l
|
UTSW |
3 |
90,117,693 (GRCm39) |
missense |
probably benign |
|
R9612:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9654:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9660:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9660:Nup210l
|
UTSW |
3 |
90,105,402 (GRCm39) |
missense |
probably benign |
0.30 |
R9662:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9682:Nup210l
|
UTSW |
3 |
90,051,469 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9729:Nup210l
|
UTSW |
3 |
90,107,173 (GRCm39) |
missense |
probably benign |
0.01 |
R9750:Nup210l
|
UTSW |
3 |
90,117,659 (GRCm39) |
critical splice acceptor site |
probably null |
|
|