Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700113H08Rik |
T |
C |
10: 87,062,083 (GRCm39) |
S178P |
probably damaging |
Het |
2610008E11Rik |
C |
T |
10: 78,903,681 (GRCm39) |
E212K |
probably damaging |
Het |
Abcc4 |
A |
T |
14: 118,832,197 (GRCm39) |
L736* |
probably null |
Het |
Acmsd |
A |
T |
1: 127,681,570 (GRCm39) |
M178L |
probably benign |
Het |
Adpgk |
T |
A |
9: 59,220,476 (GRCm39) |
M266K |
possibly damaging |
Het |
Aldh1b1 |
G |
A |
4: 45,802,909 (GRCm39) |
R149H |
possibly damaging |
Het |
Aox1 |
A |
G |
1: 58,338,927 (GRCm39) |
T307A |
probably benign |
Het |
C1galt1 |
T |
C |
6: 7,866,585 (GRCm39) |
Y144H |
probably damaging |
Het |
Cabin1 |
G |
C |
10: 75,579,117 (GRCm39) |
Q440E |
probably benign |
Het |
Casq2 |
A |
G |
3: 102,049,561 (GRCm39) |
S231G |
probably damaging |
Het |
Catsper2 |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
TAGGATGGCTTTTCTCAGGATAGCTTTTCTCAGGATGGCTTTTCTCAGGATAGCTTTTCT |
2: 121,228,053 (GRCm39) |
|
probably benign |
Het |
Cdan1 |
A |
G |
2: 120,558,342 (GRCm39) |
I490T |
probably damaging |
Het |
Cep170b |
T |
A |
12: 112,702,149 (GRCm39) |
V314E |
probably damaging |
Het |
Col4a4 |
T |
C |
1: 82,496,757 (GRCm39) |
E413G |
unknown |
Het |
Cyp3a25 |
A |
C |
5: 145,929,801 (GRCm39) |
F189L |
probably benign |
Het |
Dido1 |
T |
A |
2: 180,303,002 (GRCm39) |
H1634L |
probably benign |
Het |
Dnaja2 |
A |
C |
8: 86,275,303 (GRCm39) |
V156G |
probably benign |
Het |
Dpy19l4 |
T |
C |
4: 11,290,291 (GRCm39) |
|
probably null |
Het |
Eomes |
A |
T |
9: 118,309,567 (GRCm39) |
N240I |
possibly damaging |
Het |
Fads6 |
A |
G |
11: 115,176,229 (GRCm39) |
F199L |
probably benign |
Het |
Fbrs |
T |
C |
7: 127,086,956 (GRCm39) |
|
probably null |
Het |
Fndc4 |
T |
C |
5: 31,451,522 (GRCm39) |
E153G |
probably benign |
Het |
Fv1 |
TTCTCTCTCTCTCTC |
TTCTCTCTCTCTCTCTC |
4: 147,954,775 (GRCm39) |
|
probably null |
Het |
Fzr1 |
T |
C |
10: 81,206,057 (GRCm39) |
Y210C |
probably damaging |
Het |
Gjc2 |
T |
A |
11: 59,067,856 (GRCm39) |
M209L |
unknown |
Het |
Gpr33 |
A |
G |
12: 52,071,036 (GRCm39) |
M1T |
probably null |
Het |
Gtf2a1 |
A |
T |
12: 91,553,523 (GRCm39) |
I28N |
possibly damaging |
Het |
Ivd |
C |
T |
2: 118,703,730 (GRCm39) |
T212I |
probably damaging |
Het |
Jag1 |
A |
G |
2: 136,957,409 (GRCm39) |
V101A |
probably benign |
Het |
Kansl3 |
A |
T |
1: 36,404,701 (GRCm39) |
V83D |
possibly damaging |
Het |
Krt81 |
T |
A |
15: 101,359,006 (GRCm39) |
I249F |
probably benign |
Het |
Krtap21-1 |
G |
A |
16: 89,200,591 (GRCm39) |
S17L |
unknown |
Het |
Macf1 |
A |
T |
4: 123,302,989 (GRCm39) |
H504Q |
probably benign |
Het |
Map2 |
A |
G |
1: 66,455,983 (GRCm39) |
T1499A |
probably damaging |
Het |
Map3k9 |
T |
C |
12: 81,770,982 (GRCm39) |
T892A |
probably damaging |
Het |
Mcl1 |
G |
A |
3: 95,567,110 (GRCm39) |
V178I |
probably benign |
Het |
Mrs2 |
T |
A |
13: 25,188,937 (GRCm39) |
M126L |
probably benign |
Het |
Msantd1 |
C |
A |
5: 35,075,005 (GRCm39) |
N9K |
probably benign |
Het |
Myh9 |
C |
T |
15: 77,659,398 (GRCm39) |
R116H |
probably damaging |
Het |
Nfib |
A |
T |
4: 82,248,662 (GRCm39) |
D308E |
probably benign |
Het |
Nme2 |
T |
A |
11: 93,846,416 (GRCm39) |
I11F |
probably damaging |
Het |
Nmnat3 |
A |
G |
9: 98,292,286 (GRCm39) |
D111G |
probably benign |
Het |
Or5d37 |
T |
A |
2: 87,924,045 (GRCm39) |
L78F |
probably damaging |
Het |
Papss2 |
T |
C |
19: 32,641,827 (GRCm39) |
W501R |
probably damaging |
Het |
Parn |
A |
G |
16: 13,443,998 (GRCm39) |
I384T |
possibly damaging |
Het |
Pcdhb18 |
A |
G |
18: 37,623,864 (GRCm39) |
D398G |
possibly damaging |
Het |
Pdcl2 |
T |
C |
5: 76,465,771 (GRCm39) |
N102D |
probably benign |
Het |
Pdzrn3 |
C |
A |
6: 101,128,735 (GRCm39) |
E644* |
probably null |
Het |
Pi4ka |
T |
A |
16: 17,134,879 (GRCm39) |
|
probably benign |
Het |
Polg2 |
A |
G |
11: 106,668,040 (GRCm39) |
F216L |
probably damaging |
Het |
Prkcsh |
A |
G |
9: 21,924,457 (GRCm39) |
*522W |
probably null |
Het |
Prkcz |
G |
T |
4: 155,374,091 (GRCm39) |
D108E |
probably benign |
Het |
Pros1 |
T |
C |
16: 62,748,465 (GRCm39) |
V646A |
possibly damaging |
Het |
Ptprc |
A |
G |
1: 138,017,309 (GRCm39) |
I483T |
probably damaging |
Het |
Rabep2 |
T |
C |
7: 126,044,485 (GRCm39) |
I527T |
possibly damaging |
Het |
Rad50 |
T |
C |
11: 53,578,929 (GRCm39) |
K543R |
probably benign |
Het |
Samd4b |
A |
G |
7: 28,103,458 (GRCm39) |
I553T |
probably benign |
Het |
Sbpl |
A |
T |
17: 24,172,276 (GRCm39) |
N214K |
unknown |
Het |
Scgb2b11 |
C |
T |
7: 31,909,907 (GRCm39) |
E60K |
possibly damaging |
Het |
Sgk3 |
G |
A |
1: 9,956,284 (GRCm39) |
E331K |
probably damaging |
Het |
Snx6 |
A |
T |
12: 54,830,864 (GRCm39) |
L32Q |
probably damaging |
Het |
Srgap3 |
T |
A |
6: 112,723,924 (GRCm39) |
Q512L |
probably damaging |
Het |
Srsf12 |
A |
G |
4: 33,226,157 (GRCm39) |
D135G |
probably damaging |
Het |
Steap4 |
A |
G |
5: 8,026,858 (GRCm39) |
T274A |
probably damaging |
Het |
Svep1 |
A |
T |
4: 58,064,275 (GRCm39) |
V3236D |
probably benign |
Het |
Svep1 |
A |
T |
4: 58,120,642 (GRCm39) |
F797Y |
probably benign |
Het |
Tmem116 |
T |
C |
5: 121,605,987 (GRCm39) |
L113P |
probably damaging |
Het |
Tnfrsf1b |
A |
G |
4: 144,951,457 (GRCm39) |
V161A |
probably damaging |
Het |
Tnpo1 |
G |
T |
13: 98,991,987 (GRCm39) |
Q622K |
possibly damaging |
Het |
Top1mt |
A |
G |
15: 75,550,523 (GRCm39) |
V28A |
probably benign |
Het |
Trim25 |
T |
C |
11: 88,890,750 (GRCm39) |
S146P |
probably benign |
Het |
Tuba3b |
A |
G |
6: 145,566,935 (GRCm39) |
D392G |
possibly damaging |
Het |
Utrn |
C |
T |
10: 12,623,665 (GRCm39) |
R191Q |
probably benign |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Wdfy2 |
T |
A |
14: 63,137,748 (GRCm39) |
S84T |
probably benign |
Het |
Zfp873 |
T |
A |
10: 81,895,832 (GRCm39) |
F225I |
probably damaging |
Het |
|
Other mutations in Igf2r |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00161:Igf2r
|
APN |
17 |
12,932,877 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00534:Igf2r
|
APN |
17 |
12,958,215 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00902:Igf2r
|
APN |
17 |
12,919,245 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00903:Igf2r
|
APN |
17 |
12,902,754 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01160:Igf2r
|
APN |
17 |
12,923,662 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01380:Igf2r
|
APN |
17 |
12,914,261 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01392:Igf2r
|
APN |
17 |
12,923,236 (GRCm39) |
missense |
probably benign |
|
IGL01557:Igf2r
|
APN |
17 |
12,923,522 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01568:Igf2r
|
APN |
17 |
12,902,872 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01611:Igf2r
|
APN |
17 |
12,944,302 (GRCm39) |
nonsense |
probably null |
|
IGL01720:Igf2r
|
APN |
17 |
12,920,200 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01756:Igf2r
|
APN |
17 |
12,902,709 (GRCm39) |
missense |
probably benign |
|
IGL01839:Igf2r
|
APN |
17 |
12,923,909 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01904:Igf2r
|
APN |
17 |
12,933,798 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01965:Igf2r
|
APN |
17 |
12,923,225 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02083:Igf2r
|
APN |
17 |
12,912,079 (GRCm39) |
nonsense |
probably null |
|
IGL02095:Igf2r
|
APN |
17 |
12,920,892 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02183:Igf2r
|
APN |
17 |
12,917,403 (GRCm39) |
unclassified |
probably benign |
|
IGL02576:Igf2r
|
APN |
17 |
12,967,650 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02649:Igf2r
|
APN |
17 |
12,930,974 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02807:Igf2r
|
APN |
17 |
12,938,770 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02833:Igf2r
|
APN |
17 |
12,911,610 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02885:Igf2r
|
APN |
17 |
12,913,007 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02990:Igf2r
|
APN |
17 |
12,929,633 (GRCm39) |
splice site |
probably benign |
|
IGL03080:Igf2r
|
APN |
17 |
12,945,563 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03176:Igf2r
|
APN |
17 |
12,935,559 (GRCm39) |
missense |
probably damaging |
1.00 |
blunt
|
UTSW |
17 |
12,941,062 (GRCm39) |
missense |
probably benign |
0.02 |
brusque
|
UTSW |
17 |
12,933,838 (GRCm39) |
missense |
probably damaging |
0.98 |
gruff
|
UTSW |
17 |
12,902,984 (GRCm39) |
missense |
probably damaging |
0.96 |
outlier
|
UTSW |
17 |
12,914,201 (GRCm39) |
missense |
probably benign |
0.20 |
NA:Igf2r
|
UTSW |
17 |
12,910,849 (GRCm39) |
missense |
probably benign |
|
R0165:Igf2r
|
UTSW |
17 |
12,917,414 (GRCm39) |
missense |
probably benign |
0.07 |
R0412:Igf2r
|
UTSW |
17 |
12,902,835 (GRCm39) |
missense |
probably damaging |
0.98 |
R0523:Igf2r
|
UTSW |
17 |
12,910,951 (GRCm39) |
missense |
probably benign |
0.27 |
R0631:Igf2r
|
UTSW |
17 |
12,936,161 (GRCm39) |
splice site |
probably null |
|
R0722:Igf2r
|
UTSW |
17 |
12,934,382 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0894:Igf2r
|
UTSW |
17 |
12,910,988 (GRCm39) |
missense |
probably benign |
0.02 |
R1265:Igf2r
|
UTSW |
17 |
12,913,011 (GRCm39) |
missense |
probably damaging |
0.98 |
R1466:Igf2r
|
UTSW |
17 |
12,936,156 (GRCm39) |
splice site |
probably benign |
|
R1485:Igf2r
|
UTSW |
17 |
12,910,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R1633:Igf2r
|
UTSW |
17 |
12,945,196 (GRCm39) |
missense |
probably benign |
|
R1693:Igf2r
|
UTSW |
17 |
12,923,203 (GRCm39) |
missense |
probably damaging |
0.97 |
R1751:Igf2r
|
UTSW |
17 |
12,916,328 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1843:Igf2r
|
UTSW |
17 |
12,923,157 (GRCm39) |
critical splice donor site |
probably null |
|
R1981:Igf2r
|
UTSW |
17 |
12,952,790 (GRCm39) |
nonsense |
probably null |
|
R1994:Igf2r
|
UTSW |
17 |
12,911,625 (GRCm39) |
missense |
probably benign |
|
R2060:Igf2r
|
UTSW |
17 |
12,920,206 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2108:Igf2r
|
UTSW |
17 |
12,917,138 (GRCm39) |
missense |
probably benign |
0.02 |
R2132:Igf2r
|
UTSW |
17 |
12,941,095 (GRCm39) |
missense |
probably benign |
0.12 |
R2314:Igf2r
|
UTSW |
17 |
12,934,830 (GRCm39) |
missense |
probably benign |
0.28 |
R2349:Igf2r
|
UTSW |
17 |
12,941,198 (GRCm39) |
splice site |
probably null |
|
R2696:Igf2r
|
UTSW |
17 |
12,914,231 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2864:Igf2r
|
UTSW |
17 |
12,905,611 (GRCm39) |
missense |
probably damaging |
0.99 |
R2865:Igf2r
|
UTSW |
17 |
12,905,611 (GRCm39) |
missense |
probably damaging |
0.99 |
R3884:Igf2r
|
UTSW |
17 |
12,928,355 (GRCm39) |
missense |
probably benign |
|
R3930:Igf2r
|
UTSW |
17 |
12,924,716 (GRCm39) |
missense |
probably benign |
0.01 |
R4021:Igf2r
|
UTSW |
17 |
12,967,638 (GRCm39) |
missense |
probably damaging |
0.97 |
R4125:Igf2r
|
UTSW |
17 |
12,921,141 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4342:Igf2r
|
UTSW |
17 |
12,928,398 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4343:Igf2r
|
UTSW |
17 |
12,928,398 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4345:Igf2r
|
UTSW |
17 |
12,928,398 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4760:Igf2r
|
UTSW |
17 |
12,922,352 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4796:Igf2r
|
UTSW |
17 |
12,903,013 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4816:Igf2r
|
UTSW |
17 |
12,902,984 (GRCm39) |
missense |
probably damaging |
0.96 |
R4826:Igf2r
|
UTSW |
17 |
12,920,240 (GRCm39) |
missense |
probably damaging |
0.98 |
R4933:Igf2r
|
UTSW |
17 |
12,910,764 (GRCm39) |
splice site |
probably null |
|
R4980:Igf2r
|
UTSW |
17 |
12,922,247 (GRCm39) |
critical splice donor site |
probably null |
|
R5389:Igf2r
|
UTSW |
17 |
12,944,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R5473:Igf2r
|
UTSW |
17 |
12,914,201 (GRCm39) |
missense |
probably benign |
0.20 |
R5494:Igf2r
|
UTSW |
17 |
12,912,032 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5619:Igf2r
|
UTSW |
17 |
12,958,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R5738:Igf2r
|
UTSW |
17 |
12,936,254 (GRCm39) |
missense |
probably benign |
0.23 |
R5761:Igf2r
|
UTSW |
17 |
12,917,239 (GRCm39) |
splice site |
probably null |
|
R5794:Igf2r
|
UTSW |
17 |
12,928,332 (GRCm39) |
missense |
probably benign |
0.37 |
R6210:Igf2r
|
UTSW |
17 |
12,933,838 (GRCm39) |
missense |
probably damaging |
0.98 |
R6319:Igf2r
|
UTSW |
17 |
12,933,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R6388:Igf2r
|
UTSW |
17 |
12,902,787 (GRCm39) |
missense |
probably benign |
|
R6396:Igf2r
|
UTSW |
17 |
12,932,977 (GRCm39) |
missense |
probably benign |
0.00 |
R6584:Igf2r
|
UTSW |
17 |
12,920,137 (GRCm39) |
missense |
probably damaging |
0.99 |
R6590:Igf2r
|
UTSW |
17 |
12,910,824 (GRCm39) |
nonsense |
probably null |
|
R6591:Igf2r
|
UTSW |
17 |
12,907,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R6599:Igf2r
|
UTSW |
17 |
12,917,505 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6690:Igf2r
|
UTSW |
17 |
12,910,824 (GRCm39) |
nonsense |
probably null |
|
R6691:Igf2r
|
UTSW |
17 |
12,907,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R6752:Igf2r
|
UTSW |
17 |
12,933,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R6816:Igf2r
|
UTSW |
17 |
12,932,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R6841:Igf2r
|
UTSW |
17 |
12,922,263 (GRCm39) |
missense |
probably damaging |
0.97 |
R6877:Igf2r
|
UTSW |
17 |
12,916,228 (GRCm39) |
missense |
probably damaging |
0.97 |
R6950:Igf2r
|
UTSW |
17 |
12,937,605 (GRCm39) |
missense |
probably benign |
|
R7030:Igf2r
|
UTSW |
17 |
12,952,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R7038:Igf2r
|
UTSW |
17 |
12,917,212 (GRCm39) |
missense |
probably benign |
0.23 |
R7074:Igf2r
|
UTSW |
17 |
12,933,003 (GRCm39) |
missense |
possibly damaging |
0.57 |
R7348:Igf2r
|
UTSW |
17 |
12,922,371 (GRCm39) |
missense |
probably damaging |
0.99 |
R7413:Igf2r
|
UTSW |
17 |
12,917,115 (GRCm39) |
nonsense |
probably null |
|
R7463:Igf2r
|
UTSW |
17 |
12,929,532 (GRCm39) |
missense |
probably benign |
0.16 |
R7619:Igf2r
|
UTSW |
17 |
12,917,160 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7730:Igf2r
|
UTSW |
17 |
12,954,878 (GRCm39) |
missense |
probably damaging |
0.98 |
R7733:Igf2r
|
UTSW |
17 |
12,958,256 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7881:Igf2r
|
UTSW |
17 |
12,967,591 (GRCm39) |
missense |
probably benign |
|
R8022:Igf2r
|
UTSW |
17 |
12,937,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R8138:Igf2r
|
UTSW |
17 |
12,920,125 (GRCm39) |
missense |
probably benign |
0.32 |
R8220:Igf2r
|
UTSW |
17 |
12,910,958 (GRCm39) |
missense |
probably benign |
0.22 |
R8305:Igf2r
|
UTSW |
17 |
12,952,747 (GRCm39) |
missense |
probably benign |
|
R8359:Igf2r
|
UTSW |
17 |
12,902,748 (GRCm39) |
missense |
probably benign |
|
R8500:Igf2r
|
UTSW |
17 |
12,928,328 (GRCm39) |
missense |
probably damaging |
0.99 |
R8510:Igf2r
|
UTSW |
17 |
12,923,200 (GRCm39) |
missense |
probably benign |
0.38 |
R8933:Igf2r
|
UTSW |
17 |
12,923,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R8933:Igf2r
|
UTSW |
17 |
12,920,131 (GRCm39) |
missense |
probably damaging |
0.97 |
R8976:Igf2r
|
UTSW |
17 |
12,945,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R8994:Igf2r
|
UTSW |
17 |
12,935,537 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9059:Igf2r
|
UTSW |
17 |
12,970,180 (GRCm39) |
start codon destroyed |
probably null |
|
R9097:Igf2r
|
UTSW |
17 |
12,910,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R9127:Igf2r
|
UTSW |
17 |
12,958,238 (GRCm39) |
missense |
probably damaging |
0.98 |
R9278:Igf2r
|
UTSW |
17 |
12,914,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R9362:Igf2r
|
UTSW |
17 |
12,941,062 (GRCm39) |
missense |
probably benign |
0.02 |
R9371:Igf2r
|
UTSW |
17 |
12,924,646 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9522:Igf2r
|
UTSW |
17 |
12,917,215 (GRCm39) |
missense |
probably benign |
0.26 |
R9567:Igf2r
|
UTSW |
17 |
12,905,641 (GRCm39) |
missense |
probably damaging |
1.00 |
R9665:Igf2r
|
UTSW |
17 |
12,913,027 (GRCm39) |
missense |
probably benign |
0.17 |
R9666:Igf2r
|
UTSW |
17 |
12,945,588 (GRCm39) |
missense |
probably benign |
|
X0028:Igf2r
|
UTSW |
17 |
12,923,800 (GRCm39) |
nonsense |
probably null |
|
Z1177:Igf2r
|
UTSW |
17 |
12,916,286 (GRCm39) |
missense |
probably damaging |
0.99 |
|