Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
A |
G |
6: 128,523,223 (GRCm39) |
S1238P |
probably damaging |
Het |
Akap9 |
T |
C |
5: 4,119,089 (GRCm39) |
L3532S |
probably benign |
Het |
Ankfn1 |
A |
G |
11: 89,312,042 (GRCm39) |
L701P |
|
Het |
Aph1b |
A |
C |
9: 66,686,595 (GRCm39) |
I225S |
probably benign |
Het |
Asic4 |
A |
T |
1: 75,446,469 (GRCm39) |
H337L |
possibly damaging |
Het |
Atp8b3 |
T |
C |
10: 80,368,412 (GRCm39) |
E187G |
probably damaging |
Het |
Atp9a |
A |
G |
2: 168,517,205 (GRCm39) |
M376T |
probably benign |
Het |
Bod1l |
G |
T |
5: 41,976,220 (GRCm39) |
T1698K |
probably damaging |
Het |
Cacna2d4 |
T |
C |
6: 119,313,415 (GRCm39) |
|
probably null |
Het |
Catsper1 |
C |
A |
19: 5,390,402 (GRCm39) |
|
probably benign |
Het |
Cd248 |
T |
C |
19: 5,120,140 (GRCm39) |
S663P |
probably benign |
Het |
Crispld2 |
A |
T |
8: 120,737,488 (GRCm39) |
M80L |
possibly damaging |
Het |
Cwc22 |
G |
A |
2: 77,726,659 (GRCm39) |
Q807* |
probably null |
Het |
Cyp2a4 |
T |
C |
7: 26,014,136 (GRCm39) |
Y438H |
probably benign |
Het |
Cyp2b23 |
A |
T |
7: 26,381,189 (GRCm39) |
|
probably benign |
Het |
Dsp |
T |
A |
13: 38,377,126 (GRCm39) |
V1637D |
probably benign |
Het |
Elovl1 |
A |
T |
4: 118,289,156 (GRCm39) |
Y227F |
possibly damaging |
Het |
Ern1 |
T |
C |
11: 106,300,946 (GRCm39) |
K483E |
probably benign |
Het |
Fzd2 |
T |
C |
11: 102,496,465 (GRCm39) |
F303S |
probably benign |
Het |
Gm9944 |
A |
T |
4: 144,179,763 (GRCm39) |
V42D |
unknown |
Het |
Grik5 |
G |
A |
7: 24,767,429 (GRCm39) |
|
probably benign |
Het |
Hdac4 |
T |
C |
1: 91,909,929 (GRCm39) |
D445G |
probably benign |
Het |
Hinfp |
C |
T |
9: 44,209,062 (GRCm39) |
R352H |
probably damaging |
Het |
Hrnr |
A |
G |
3: 93,231,277 (GRCm39) |
H505R |
unknown |
Het |
Hsfy2 |
C |
T |
1: 56,675,752 (GRCm39) |
D262N |
probably benign |
Het |
Hspa4 |
G |
A |
11: 53,174,463 (GRCm39) |
Q186* |
probably null |
Het |
Ipo8 |
T |
C |
6: 148,700,125 (GRCm39) |
H584R |
probably benign |
Het |
Krtap8-1 |
T |
A |
16: 89,284,636 (GRCm39) |
R54* |
probably null |
Het |
Lekr1 |
T |
A |
3: 65,591,426 (GRCm39) |
Y54* |
probably null |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Lypd10 |
A |
G |
7: 24,413,170 (GRCm39) |
D163G |
probably benign |
Het |
Lzts3 |
A |
T |
2: 130,476,865 (GRCm39) |
Y528N |
possibly damaging |
Het |
Mdn1 |
T |
A |
4: 32,676,812 (GRCm39) |
V628E |
probably benign |
Het |
Mgat5b |
A |
C |
11: 116,859,348 (GRCm39) |
|
probably benign |
Het |
Mical2 |
A |
C |
7: 111,870,589 (GRCm39) |
K26T |
possibly damaging |
Het |
Mllt10 |
C |
T |
2: 18,167,404 (GRCm39) |
S443L |
probably benign |
Het |
Mtf1 |
G |
A |
4: 124,698,913 (GRCm39) |
|
probably benign |
Het |
Myom2 |
T |
C |
8: 15,154,068 (GRCm39) |
F669L |
probably damaging |
Het |
Nlrp9c |
A |
T |
7: 26,077,428 (GRCm39) |
|
probably null |
Het |
Nog |
G |
C |
11: 89,192,602 (GRCm39) |
S82W |
probably damaging |
Het |
Ntrk2 |
A |
G |
13: 59,276,084 (GRCm39) |
T795A |
probably benign |
Het |
Or4a78 |
A |
G |
2: 89,497,930 (GRCm39) |
F100S |
probably damaging |
Het |
Or56a3b |
G |
A |
7: 104,771,223 (GRCm39) |
M186I |
probably benign |
Het |
Or5m3 |
A |
T |
2: 85,838,356 (GRCm39) |
M79L |
|
Het |
Or5w17 |
A |
T |
2: 87,584,048 (GRCm39) |
F96L |
probably benign |
Het |
Pira12 |
C |
A |
7: 3,898,500 (GRCm39) |
|
probably null |
Het |
Prl6a1 |
A |
T |
13: 27,502,064 (GRCm39) |
I144L |
|
Het |
Rab11fip5 |
A |
G |
6: 85,317,892 (GRCm39) |
V999A |
probably benign |
Het |
Serpinb6b |
TTGTTTCTGT |
TTGT |
13: 33,162,139 (GRCm39) |
|
probably benign |
Het |
Shisa6 |
A |
G |
11: 66,110,853 (GRCm39) |
M296T |
probably benign |
Het |
Slc18a1 |
T |
A |
8: 69,491,533 (GRCm39) |
T494S |
probably benign |
Het |
Slc22a29 |
T |
G |
19: 8,146,669 (GRCm39) |
I378L |
probably benign |
Het |
Slc23a2 |
C |
T |
2: 131,920,332 (GRCm39) |
|
probably null |
Het |
Slc2a7 |
G |
T |
4: 150,243,001 (GRCm39) |
R274L |
probably benign |
Het |
Spta1 |
A |
G |
1: 174,058,911 (GRCm39) |
T1949A |
possibly damaging |
Het |
Szt2 |
A |
G |
4: 118,221,866 (GRCm39) |
V3339A |
unknown |
Het |
Tcp10a |
G |
A |
17: 7,593,935 (GRCm39) |
D87N |
probably benign |
Het |
Tgm5 |
T |
G |
2: 120,877,270 (GRCm39) |
Q638P |
probably damaging |
Het |
Tmem145 |
A |
G |
7: 25,014,265 (GRCm39) |
T460A |
possibly damaging |
Het |
Ttc3 |
A |
T |
16: 94,185,208 (GRCm39) |
M50L |
probably benign |
Het |
Ush1c |
A |
G |
7: 45,854,629 (GRCm39) |
S708P |
probably benign |
Het |
Vmn1r217 |
T |
A |
13: 23,298,876 (GRCm39) |
T9S |
probably benign |
Het |
Vmn1r26 |
T |
C |
6: 57,985,373 (GRCm39) |
Y272C |
|
Het |
Vmn1r75 |
G |
T |
7: 11,614,513 (GRCm39) |
A82S |
probably benign |
Het |
Vmn2r117 |
T |
A |
17: 23,678,918 (GRCm39) |
R769* |
probably null |
Het |
Vps13b |
C |
A |
15: 35,448,793 (GRCm39) |
A589E |
probably damaging |
Het |
Vps13d |
G |
A |
4: 144,898,249 (GRCm39) |
R304W |
|
Het |
Vps41 |
A |
G |
13: 19,011,775 (GRCm39) |
E294G |
probably benign |
Het |
Xpo7 |
T |
C |
14: 70,909,113 (GRCm39) |
T802A |
probably benign |
Het |
Ylpm1 |
T |
A |
12: 85,104,052 (GRCm39) |
D2022E |
|
Het |
Zfp433 |
T |
A |
10: 81,555,724 (GRCm39) |
C75* |
probably null |
Het |
Zyg11a |
A |
T |
4: 108,039,009 (GRCm39) |
S737T |
probably benign |
Het |
|
Other mutations in Lama4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Lama4
|
APN |
10 |
38,941,591 (GRCm39) |
splice site |
probably benign |
|
IGL00091:Lama4
|
APN |
10 |
38,948,801 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00429:Lama4
|
APN |
10 |
38,887,022 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL00430:Lama4
|
APN |
10 |
38,921,700 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL01074:Lama4
|
APN |
10 |
38,974,484 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01386:Lama4
|
APN |
10 |
38,887,060 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01603:Lama4
|
APN |
10 |
38,941,642 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01643:Lama4
|
APN |
10 |
38,932,846 (GRCm39) |
missense |
probably benign |
|
IGL01655:Lama4
|
APN |
10 |
38,936,209 (GRCm39) |
missense |
probably benign |
|
IGL01954:Lama4
|
APN |
10 |
38,963,295 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01984:Lama4
|
APN |
10 |
38,951,525 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02193:Lama4
|
APN |
10 |
38,918,670 (GRCm39) |
missense |
probably benign |
|
IGL02290:Lama4
|
APN |
10 |
38,893,360 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02441:Lama4
|
APN |
10 |
38,937,441 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02549:Lama4
|
APN |
10 |
38,936,200 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02797:Lama4
|
APN |
10 |
38,932,920 (GRCm39) |
missense |
probably null |
0.00 |
IGL02819:Lama4
|
APN |
10 |
38,902,565 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL03122:Lama4
|
APN |
10 |
38,943,959 (GRCm39) |
missense |
probably benign |
|
IGL03184:Lama4
|
APN |
10 |
38,954,839 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03307:Lama4
|
APN |
10 |
38,893,379 (GRCm39) |
missense |
probably benign |
|
BB006:Lama4
|
UTSW |
10 |
38,954,843 (GRCm39) |
missense |
probably damaging |
1.00 |
BB016:Lama4
|
UTSW |
10 |
38,954,843 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4585001:Lama4
|
UTSW |
10 |
38,950,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R0003:Lama4
|
UTSW |
10 |
38,936,218 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0015:Lama4
|
UTSW |
10 |
38,951,432 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0015:Lama4
|
UTSW |
10 |
38,951,432 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0035:Lama4
|
UTSW |
10 |
38,948,734 (GRCm39) |
missense |
probably benign |
0.01 |
R0141:Lama4
|
UTSW |
10 |
38,968,274 (GRCm39) |
missense |
probably benign |
0.05 |
R0257:Lama4
|
UTSW |
10 |
38,970,880 (GRCm39) |
splice site |
probably benign |
|
R0267:Lama4
|
UTSW |
10 |
38,904,635 (GRCm39) |
missense |
probably damaging |
0.96 |
R0557:Lama4
|
UTSW |
10 |
38,964,393 (GRCm39) |
missense |
probably benign |
0.38 |
R1052:Lama4
|
UTSW |
10 |
38,968,241 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1248:Lama4
|
UTSW |
10 |
38,932,843 (GRCm39) |
missense |
probably damaging |
0.99 |
R1249:Lama4
|
UTSW |
10 |
38,951,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R1291:Lama4
|
UTSW |
10 |
38,924,065 (GRCm39) |
missense |
probably benign |
0.00 |
R1307:Lama4
|
UTSW |
10 |
38,946,028 (GRCm39) |
missense |
probably benign |
0.06 |
R1404:Lama4
|
UTSW |
10 |
38,937,387 (GRCm39) |
missense |
probably benign |
0.09 |
R1404:Lama4
|
UTSW |
10 |
38,937,387 (GRCm39) |
missense |
probably benign |
0.09 |
R1443:Lama4
|
UTSW |
10 |
38,949,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R1499:Lama4
|
UTSW |
10 |
38,964,876 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1616:Lama4
|
UTSW |
10 |
38,951,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1691:Lama4
|
UTSW |
10 |
38,956,559 (GRCm39) |
missense |
probably benign |
0.09 |
R1748:Lama4
|
UTSW |
10 |
38,941,615 (GRCm39) |
missense |
probably benign |
0.01 |
R1768:Lama4
|
UTSW |
10 |
38,979,497 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1772:Lama4
|
UTSW |
10 |
38,936,220 (GRCm39) |
missense |
probably benign |
0.00 |
R1813:Lama4
|
UTSW |
10 |
38,936,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1813:Lama4
|
UTSW |
10 |
38,909,121 (GRCm39) |
splice site |
probably benign |
|
R1897:Lama4
|
UTSW |
10 |
38,936,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1907:Lama4
|
UTSW |
10 |
38,948,754 (GRCm39) |
missense |
probably benign |
0.13 |
R1943:Lama4
|
UTSW |
10 |
38,973,134 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2041:Lama4
|
UTSW |
10 |
38,945,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R2242:Lama4
|
UTSW |
10 |
38,902,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R2300:Lama4
|
UTSW |
10 |
38,963,316 (GRCm39) |
missense |
probably benign |
|
R2326:Lama4
|
UTSW |
10 |
38,918,563 (GRCm39) |
splice site |
probably null |
|
R2570:Lama4
|
UTSW |
10 |
38,982,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R2570:Lama4
|
UTSW |
10 |
38,951,354 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2571:Lama4
|
UTSW |
10 |
38,918,671 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2887:Lama4
|
UTSW |
10 |
38,968,250 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2926:Lama4
|
UTSW |
10 |
38,954,828 (GRCm39) |
missense |
probably benign |
0.16 |
R3237:Lama4
|
UTSW |
10 |
38,973,175 (GRCm39) |
missense |
probably damaging |
0.97 |
R4095:Lama4
|
UTSW |
10 |
38,973,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R4151:Lama4
|
UTSW |
10 |
38,881,424 (GRCm39) |
missense |
probably benign |
0.00 |
R4470:Lama4
|
UTSW |
10 |
38,956,492 (GRCm39) |
nonsense |
probably null |
|
R4812:Lama4
|
UTSW |
10 |
38,948,765 (GRCm39) |
missense |
probably benign |
|
R4822:Lama4
|
UTSW |
10 |
38,909,049 (GRCm39) |
missense |
probably benign |
0.01 |
R4997:Lama4
|
UTSW |
10 |
38,968,262 (GRCm39) |
missense |
probably damaging |
0.99 |
R5119:Lama4
|
UTSW |
10 |
38,924,050 (GRCm39) |
missense |
probably benign |
0.00 |
R5468:Lama4
|
UTSW |
10 |
38,948,678 (GRCm39) |
splice site |
probably null |
|
R5909:Lama4
|
UTSW |
10 |
38,948,855 (GRCm39) |
missense |
probably benign |
0.00 |
R5917:Lama4
|
UTSW |
10 |
38,924,028 (GRCm39) |
missense |
probably benign |
0.10 |
R5927:Lama4
|
UTSW |
10 |
38,948,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R5950:Lama4
|
UTSW |
10 |
38,906,444 (GRCm39) |
missense |
probably benign |
0.03 |
R6051:Lama4
|
UTSW |
10 |
38,943,898 (GRCm39) |
missense |
probably benign |
0.01 |
R6277:Lama4
|
UTSW |
10 |
38,982,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R6294:Lama4
|
UTSW |
10 |
38,951,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R6372:Lama4
|
UTSW |
10 |
38,943,948 (GRCm39) |
missense |
probably benign |
|
R6532:Lama4
|
UTSW |
10 |
38,924,073 (GRCm39) |
missense |
possibly damaging |
0.58 |
R6547:Lama4
|
UTSW |
10 |
38,949,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R6578:Lama4
|
UTSW |
10 |
38,893,361 (GRCm39) |
missense |
probably benign |
0.01 |
R6737:Lama4
|
UTSW |
10 |
38,970,907 (GRCm39) |
missense |
probably damaging |
0.96 |
R6987:Lama4
|
UTSW |
10 |
38,950,275 (GRCm39) |
missense |
probably benign |
0.00 |
R7040:Lama4
|
UTSW |
10 |
38,936,158 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7139:Lama4
|
UTSW |
10 |
38,951,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R7188:Lama4
|
UTSW |
10 |
38,841,729 (GRCm39) |
start gained |
probably benign |
|
R7189:Lama4
|
UTSW |
10 |
38,841,729 (GRCm39) |
start gained |
probably benign |
|
R7199:Lama4
|
UTSW |
10 |
38,956,536 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7211:Lama4
|
UTSW |
10 |
38,881,491 (GRCm39) |
missense |
probably damaging |
0.98 |
R7262:Lama4
|
UTSW |
10 |
38,970,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R7274:Lama4
|
UTSW |
10 |
38,968,295 (GRCm39) |
missense |
probably benign |
0.00 |
R7311:Lama4
|
UTSW |
10 |
38,902,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R7391:Lama4
|
UTSW |
10 |
38,963,383 (GRCm39) |
critical splice donor site |
probably null |
|
R7399:Lama4
|
UTSW |
10 |
38,923,944 (GRCm39) |
missense |
probably damaging |
0.98 |
R7426:Lama4
|
UTSW |
10 |
38,921,751 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7472:Lama4
|
UTSW |
10 |
38,963,369 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7635:Lama4
|
UTSW |
10 |
38,968,184 (GRCm39) |
missense |
probably benign |
|
R7775:Lama4
|
UTSW |
10 |
38,954,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R7805:Lama4
|
UTSW |
10 |
38,902,747 (GRCm39) |
critical splice donor site |
probably null |
|
R7885:Lama4
|
UTSW |
10 |
38,964,840 (GRCm39) |
missense |
probably benign |
0.01 |
R7895:Lama4
|
UTSW |
10 |
38,964,325 (GRCm39) |
missense |
probably damaging |
0.96 |
R7910:Lama4
|
UTSW |
10 |
38,946,005 (GRCm39) |
missense |
probably damaging |
0.99 |
R7929:Lama4
|
UTSW |
10 |
38,954,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R7952:Lama4
|
UTSW |
10 |
38,906,486 (GRCm39) |
missense |
probably benign |
0.39 |
R7991:Lama4
|
UTSW |
10 |
38,921,805 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8059:Lama4
|
UTSW |
10 |
38,842,057 (GRCm39) |
missense |
probably benign |
0.00 |
R8194:Lama4
|
UTSW |
10 |
38,954,716 (GRCm39) |
missense |
probably damaging |
0.99 |
R8248:Lama4
|
UTSW |
10 |
38,937,375 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8252:Lama4
|
UTSW |
10 |
38,936,142 (GRCm39) |
missense |
probably benign |
0.00 |
R8265:Lama4
|
UTSW |
10 |
38,981,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R8275:Lama4
|
UTSW |
10 |
38,948,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R8426:Lama4
|
UTSW |
10 |
38,979,487 (GRCm39) |
missense |
probably damaging |
0.98 |
R8434:Lama4
|
UTSW |
10 |
38,902,703 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8720:Lama4
|
UTSW |
10 |
38,971,079 (GRCm39) |
missense |
probably damaging |
0.97 |
R8792:Lama4
|
UTSW |
10 |
38,924,048 (GRCm39) |
missense |
probably benign |
0.00 |
R8836:Lama4
|
UTSW |
10 |
38,902,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R8867:Lama4
|
UTSW |
10 |
38,923,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R8892:Lama4
|
UTSW |
10 |
38,973,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R8913:Lama4
|
UTSW |
10 |
38,982,039 (GRCm39) |
missense |
probably benign |
0.10 |
R9177:Lama4
|
UTSW |
10 |
38,950,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R9187:Lama4
|
UTSW |
10 |
38,924,124 (GRCm39) |
critical splice donor site |
probably null |
|
R9193:Lama4
|
UTSW |
10 |
38,951,444 (GRCm39) |
missense |
probably benign |
0.03 |
R9268:Lama4
|
UTSW |
10 |
38,950,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R9287:Lama4
|
UTSW |
10 |
38,981,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R9295:Lama4
|
UTSW |
10 |
38,948,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R9303:Lama4
|
UTSW |
10 |
38,973,137 (GRCm39) |
missense |
probably damaging |
0.99 |
R9330:Lama4
|
UTSW |
10 |
38,954,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R9430:Lama4
|
UTSW |
10 |
38,921,802 (GRCm39) |
missense |
probably null |
|
R9572:Lama4
|
UTSW |
10 |
38,959,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R9636:Lama4
|
UTSW |
10 |
38,956,500 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9663:Lama4
|
UTSW |
10 |
38,923,944 (GRCm39) |
missense |
probably damaging |
0.98 |
R9777:Lama4
|
UTSW |
10 |
38,924,101 (GRCm39) |
missense |
probably benign |
0.00 |
X0067:Lama4
|
UTSW |
10 |
38,921,688 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Lama4
|
UTSW |
10 |
38,881,421 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Lama4
|
UTSW |
10 |
38,881,420 (GRCm39) |
nonsense |
probably null |
|
|