Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
G |
T |
11: 109,684,980 (GRCm39) |
C172* |
probably null |
Het |
9930111J21Rik1 |
G |
A |
11: 48,838,533 (GRCm39) |
R685W |
probably damaging |
Het |
Arhgap10 |
A |
T |
8: 78,109,386 (GRCm39) |
L399H |
probably damaging |
Het |
Arih2 |
AGCCG |
AG |
9: 108,488,859 (GRCm39) |
|
probably benign |
Het |
Atp13a2 |
A |
G |
4: 140,728,132 (GRCm39) |
H575R |
possibly damaging |
Het |
Bbof1 |
G |
A |
12: 84,458,044 (GRCm39) |
|
probably null |
Het |
Bltp3a |
A |
G |
17: 28,105,838 (GRCm39) |
E788G |
probably damaging |
Het |
Catsperg2 |
A |
C |
7: 29,409,559 (GRCm39) |
Y545D |
possibly damaging |
Het |
Cdc42bpa |
T |
A |
1: 179,892,580 (GRCm39) |
I248N |
probably damaging |
Het |
Cdk11b |
A |
T |
4: 155,733,282 (GRCm39) |
|
probably benign |
Het |
Cfap46 |
C |
A |
7: 139,183,776 (GRCm39) |
L90F |
probably benign |
Het |
Cndp2 |
A |
G |
18: 84,688,954 (GRCm39) |
L276P |
possibly damaging |
Het |
Col3a1 |
A |
C |
1: 45,385,270 (GRCm39) |
D129A |
probably damaging |
Het |
Daam1 |
C |
A |
12: 71,993,294 (GRCm39) |
H354Q |
unknown |
Het |
Dnah5 |
T |
A |
15: 28,421,824 (GRCm39) |
F3892Y |
probably damaging |
Het |
Dnajb3 |
A |
G |
1: 88,132,745 (GRCm39) |
V219A |
possibly damaging |
Het |
Drd5 |
A |
G |
5: 38,477,544 (GRCm39) |
H179R |
probably damaging |
Het |
Dym |
A |
G |
18: 75,252,232 (GRCm39) |
N333D |
possibly damaging |
Het |
Eif2b3 |
A |
G |
4: 116,909,933 (GRCm39) |
D156G |
probably damaging |
Het |
Emc1 |
A |
G |
4: 139,099,007 (GRCm39) |
D830G |
probably damaging |
Het |
F13a1 |
A |
C |
13: 37,172,830 (GRCm39) |
I183M |
probably damaging |
Het |
Fam136b-ps |
T |
A |
15: 31,277,043 (GRCm39) |
|
probably benign |
Het |
Fdft1 |
C |
A |
14: 63,400,853 (GRCm39) |
K93N |
probably damaging |
Het |
Garre1 |
C |
T |
7: 33,945,237 (GRCm39) |
G336S |
probably benign |
Het |
Gcc2 |
A |
G |
10: 58,114,628 (GRCm39) |
D959G |
probably damaging |
Het |
Gp2 |
A |
G |
7: 119,053,514 (GRCm39) |
V149A |
probably damaging |
Het |
Gpc1 |
G |
A |
1: 92,784,751 (GRCm39) |
G308D |
probably damaging |
Het |
Hdac9 |
A |
T |
12: 34,423,906 (GRCm39) |
C587S |
probably benign |
Het |
Hspg2 |
C |
T |
4: 137,246,251 (GRCm39) |
R1010C |
probably damaging |
Het |
Iars2 |
A |
G |
1: 185,050,125 (GRCm39) |
V453A |
possibly damaging |
Het |
Il1r1 |
T |
G |
1: 40,332,684 (GRCm39) |
C121W |
probably damaging |
Het |
Inhca |
A |
G |
9: 103,156,613 (GRCm39) |
V149A |
probably benign |
Het |
Jazf1 |
A |
G |
6: 52,754,525 (GRCm39) |
Y184H |
probably damaging |
Het |
Kel |
A |
T |
6: 41,675,989 (GRCm39) |
Y234N |
probably damaging |
Het |
Khk |
G |
A |
5: 31,087,004 (GRCm39) |
G186D |
probably damaging |
Het |
Klf4 |
A |
T |
4: 55,530,301 (GRCm39) |
M270K |
probably benign |
Het |
Kmt2c |
G |
A |
5: 25,519,706 (GRCm39) |
L2135F |
probably benign |
Het |
Krtap15-1 |
A |
G |
16: 88,626,044 (GRCm39) |
Y37C |
probably damaging |
Het |
Lars1 |
A |
G |
18: 42,347,841 (GRCm39) |
F994S |
possibly damaging |
Het |
Ldc1 |
C |
T |
4: 130,115,408 (GRCm39) |
|
probably null |
Het |
Lrp8 |
T |
C |
4: 107,691,952 (GRCm39) |
|
probably null |
Het |
Lrrc2 |
A |
T |
9: 110,809,987 (GRCm39) |
D341V |
probably damaging |
Het |
Map4k4 |
A |
G |
1: 40,046,662 (GRCm39) |
K646R |
probably damaging |
Het |
Mrps9 |
T |
A |
1: 42,934,491 (GRCm39) |
|
probably null |
Het |
Or10ag60 |
T |
A |
2: 87,438,055 (GRCm39) |
C108S |
probably damaging |
Het |
Or11h6 |
T |
A |
14: 50,880,619 (GRCm39) |
Y288N |
probably damaging |
Het |
Or8c20 |
C |
T |
9: 38,260,924 (GRCm39) |
H176Y |
probably damaging |
Het |
Pcnt |
A |
T |
10: 76,235,779 (GRCm39) |
C1401S |
possibly damaging |
Het |
Pdgfrb |
A |
T |
18: 61,210,740 (GRCm39) |
K749M |
probably damaging |
Het |
Pigo |
A |
T |
4: 43,019,412 (GRCm39) |
W969R |
probably null |
Het |
Pigr |
A |
T |
1: 130,772,436 (GRCm39) |
Y218F |
probably damaging |
Het |
Pih1d1 |
A |
G |
7: 44,804,278 (GRCm39) |
|
probably benign |
Het |
Pik3cg |
A |
T |
12: 32,249,195 (GRCm39) |
|
probably null |
Het |
Pik3r6 |
A |
T |
11: 68,424,294 (GRCm39) |
K300* |
probably null |
Het |
Pip5k1c |
A |
G |
10: 81,141,084 (GRCm39) |
D64G |
probably damaging |
Het |
Piwil2 |
A |
T |
14: 70,659,042 (GRCm39) |
I161K |
possibly damaging |
Het |
Pou3f1 |
A |
G |
4: 124,552,449 (GRCm39) |
E317G |
probably damaging |
Het |
Prdm8 |
C |
T |
5: 98,333,071 (GRCm39) |
Q213* |
probably null |
Het |
Prpf6 |
T |
A |
2: 181,291,899 (GRCm39) |
C739S |
possibly damaging |
Het |
Psmc3 |
T |
A |
2: 90,884,953 (GRCm39) |
S40T |
probably benign |
Het |
Psmd3 |
A |
T |
11: 98,573,650 (GRCm39) |
D32V |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Rapgef6 |
A |
T |
11: 54,582,207 (GRCm39) |
H1373L |
possibly damaging |
Het |
Rnf207 |
A |
C |
4: 152,397,666 (GRCm39) |
S328A |
probably benign |
Het |
Ros1 |
C |
T |
10: 52,004,512 (GRCm39) |
|
probably null |
Het |
Ryr2 |
T |
A |
13: 11,602,140 (GRCm39) |
I4581F |
possibly damaging |
Het |
Sacm1l |
C |
T |
9: 123,415,464 (GRCm39) |
R480W |
probably damaging |
Het |
Selenoo |
T |
A |
15: 88,976,969 (GRCm39) |
M207K |
probably damaging |
Het |
Sh3tc2 |
G |
A |
18: 62,147,962 (GRCm39) |
|
probably null |
Het |
Slc28a2b |
T |
A |
2: 122,353,395 (GRCm39) |
|
probably null |
Het |
Slco2b1 |
G |
T |
7: 99,309,256 (GRCm39) |
Q692K |
probably benign |
Het |
Slfn4 |
A |
T |
11: 83,077,623 (GRCm39) |
D137V |
probably damaging |
Het |
Srrm2 |
G |
A |
17: 24,039,592 (GRCm39) |
A2175T |
probably damaging |
Het |
Stard9 |
T |
A |
2: 120,523,880 (GRCm39) |
C692S |
probably benign |
Het |
Sulf2 |
T |
A |
2: 165,923,542 (GRCm39) |
D559V |
probably benign |
Het |
Tbpl2 |
T |
C |
2: 23,977,170 (GRCm39) |
I283V |
probably benign |
Het |
Tmem19 |
A |
G |
10: 115,195,666 (GRCm39) |
F46S |
probably benign |
Het |
Trp63 |
T |
A |
16: 25,582,056 (GRCm39) |
Y35N |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,716,786 (GRCm39) |
|
probably benign |
Het |
Ube2z |
A |
T |
11: 95,941,148 (GRCm39) |
H331Q |
probably benign |
Het |
Ubr1 |
C |
T |
2: 120,742,478 (GRCm39) |
|
probably null |
Het |
Vmn1r235 |
A |
T |
17: 21,482,550 (GRCm39) |
I292F |
possibly damaging |
Het |
Vmn2r1 |
T |
A |
3: 64,012,501 (GRCm39) |
D787E |
probably damaging |
Het |
Vmn2r3 |
A |
G |
3: 64,167,220 (GRCm39) |
V637A |
probably benign |
Het |
Xpnpep1 |
C |
A |
19: 52,994,606 (GRCm39) |
V341L |
probably benign |
Het |
Yme1l1 |
A |
G |
2: 23,084,759 (GRCm39) |
D619G |
probably damaging |
Het |
Zfp597 |
G |
A |
16: 3,684,502 (GRCm39) |
P85S |
probably damaging |
Het |
Zscan20 |
A |
G |
4: 128,479,921 (GRCm39) |
S857P |
probably benign |
Het |
|
Other mutations in Sec16a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00337:Sec16a
|
APN |
2 |
26,329,499 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00435:Sec16a
|
APN |
2 |
26,320,113 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00469:Sec16a
|
APN |
2 |
26,318,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01622:Sec16a
|
APN |
2 |
26,328,915 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01623:Sec16a
|
APN |
2 |
26,328,915 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02158:Sec16a
|
APN |
2 |
26,306,644 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02188:Sec16a
|
APN |
2 |
26,326,020 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02445:Sec16a
|
APN |
2 |
26,312,052 (GRCm39) |
missense |
probably benign |
|
IGL02568:Sec16a
|
APN |
2 |
26,326,054 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02710:Sec16a
|
APN |
2 |
26,320,142 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02735:Sec16a
|
APN |
2 |
26,318,149 (GRCm39) |
splice site |
probably benign |
|
IGL02964:Sec16a
|
APN |
2 |
26,309,735 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03027:Sec16a
|
APN |
2 |
26,313,601 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03073:Sec16a
|
APN |
2 |
26,329,195 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03297:Sec16a
|
APN |
2 |
26,329,202 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03339:Sec16a
|
APN |
2 |
26,325,945 (GRCm39) |
missense |
probably benign |
|
H8562:Sec16a
|
UTSW |
2 |
26,331,517 (GRCm39) |
missense |
probably benign |
|
IGL03050:Sec16a
|
UTSW |
2 |
26,305,759 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4486001:Sec16a
|
UTSW |
2 |
26,315,785 (GRCm39) |
missense |
|
|
R0039:Sec16a
|
UTSW |
2 |
26,313,926 (GRCm39) |
missense |
probably benign |
0.03 |
R0095:Sec16a
|
UTSW |
2 |
26,315,772 (GRCm39) |
splice site |
probably null |
|
R0095:Sec16a
|
UTSW |
2 |
26,315,772 (GRCm39) |
splice site |
probably null |
|
R0189:Sec16a
|
UTSW |
2 |
26,314,426 (GRCm39) |
splice site |
probably null |
|
R0255:Sec16a
|
UTSW |
2 |
26,321,198 (GRCm39) |
missense |
probably damaging |
0.97 |
R0278:Sec16a
|
UTSW |
2 |
26,318,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R0739:Sec16a
|
UTSW |
2 |
26,331,063 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0743:Sec16a
|
UTSW |
2 |
26,309,734 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1446:Sec16a
|
UTSW |
2 |
26,313,579 (GRCm39) |
missense |
probably benign |
0.00 |
R1466:Sec16a
|
UTSW |
2 |
26,321,169 (GRCm39) |
missense |
probably damaging |
0.98 |
R1466:Sec16a
|
UTSW |
2 |
26,321,169 (GRCm39) |
missense |
probably damaging |
0.98 |
R1501:Sec16a
|
UTSW |
2 |
26,330,057 (GRCm39) |
missense |
probably benign |
0.16 |
R1524:Sec16a
|
UTSW |
2 |
26,318,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R1584:Sec16a
|
UTSW |
2 |
26,321,169 (GRCm39) |
missense |
probably damaging |
0.98 |
R1649:Sec16a
|
UTSW |
2 |
26,315,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R1744:Sec16a
|
UTSW |
2 |
26,329,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Sec16a
|
UTSW |
2 |
26,320,144 (GRCm39) |
missense |
probably benign |
0.00 |
R1973:Sec16a
|
UTSW |
2 |
26,316,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2005:Sec16a
|
UTSW |
2 |
26,329,092 (GRCm39) |
missense |
probably benign |
0.27 |
R2073:Sec16a
|
UTSW |
2 |
26,330,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2074:Sec16a
|
UTSW |
2 |
26,330,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Sec16a
|
UTSW |
2 |
26,330,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Sec16a
|
UTSW |
2 |
26,303,757 (GRCm39) |
intron |
probably benign |
|
R2472:Sec16a
|
UTSW |
2 |
26,329,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R2512:Sec16a
|
UTSW |
2 |
26,329,037 (GRCm39) |
missense |
probably benign |
0.00 |
R2520:Sec16a
|
UTSW |
2 |
26,331,368 (GRCm39) |
nonsense |
probably null |
|
R2571:Sec16a
|
UTSW |
2 |
26,329,343 (GRCm39) |
missense |
probably benign |
0.08 |
R3105:Sec16a
|
UTSW |
2 |
26,328,433 (GRCm39) |
missense |
probably benign |
0.14 |
R3508:Sec16a
|
UTSW |
2 |
26,315,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R3809:Sec16a
|
UTSW |
2 |
26,331,825 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3912:Sec16a
|
UTSW |
2 |
26,304,399 (GRCm39) |
missense |
probably damaging |
0.97 |
R4292:Sec16a
|
UTSW |
2 |
26,312,167 (GRCm39) |
missense |
probably benign |
0.01 |
R4293:Sec16a
|
UTSW |
2 |
26,312,167 (GRCm39) |
missense |
probably benign |
0.01 |
R4294:Sec16a
|
UTSW |
2 |
26,312,167 (GRCm39) |
missense |
probably benign |
0.01 |
R4576:Sec16a
|
UTSW |
2 |
26,321,131 (GRCm39) |
nonsense |
probably null |
|
R4611:Sec16a
|
UTSW |
2 |
26,331,817 (GRCm39) |
missense |
probably benign |
0.04 |
R4627:Sec16a
|
UTSW |
2 |
26,321,080 (GRCm39) |
splice site |
probably null |
|
R4627:Sec16a
|
UTSW |
2 |
26,319,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4662:Sec16a
|
UTSW |
2 |
26,320,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R4665:Sec16a
|
UTSW |
2 |
26,302,970 (GRCm39) |
intron |
probably benign |
|
R4906:Sec16a
|
UTSW |
2 |
26,331,979 (GRCm39) |
unclassified |
probably benign |
|
R4967:Sec16a
|
UTSW |
2 |
26,302,883 (GRCm39) |
missense |
probably benign |
0.00 |
R4983:Sec16a
|
UTSW |
2 |
26,329,531 (GRCm39) |
missense |
probably benign |
|
R5251:Sec16a
|
UTSW |
2 |
26,329,357 (GRCm39) |
missense |
probably benign |
0.00 |
R5391:Sec16a
|
UTSW |
2 |
26,330,044 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5457:Sec16a
|
UTSW |
2 |
26,330,280 (GRCm39) |
missense |
probably benign |
0.01 |
R5530:Sec16a
|
UTSW |
2 |
26,329,264 (GRCm39) |
missense |
probably benign |
0.00 |
R5645:Sec16a
|
UTSW |
2 |
26,329,907 (GRCm39) |
missense |
probably benign |
0.01 |
R5661:Sec16a
|
UTSW |
2 |
26,329,649 (GRCm39) |
missense |
probably benign |
0.01 |
R5770:Sec16a
|
UTSW |
2 |
26,304,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R5830:Sec16a
|
UTSW |
2 |
26,330,853 (GRCm39) |
missense |
probably benign |
0.15 |
R5866:Sec16a
|
UTSW |
2 |
26,309,650 (GRCm39) |
missense |
probably benign |
0.00 |
R5875:Sec16a
|
UTSW |
2 |
26,323,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R5906:Sec16a
|
UTSW |
2 |
26,328,843 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5922:Sec16a
|
UTSW |
2 |
26,305,651 (GRCm39) |
missense |
probably benign |
0.05 |
R6076:Sec16a
|
UTSW |
2 |
26,313,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Sec16a
|
UTSW |
2 |
26,316,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R6295:Sec16a
|
UTSW |
2 |
26,318,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Sec16a
|
UTSW |
2 |
26,315,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R6309:Sec16a
|
UTSW |
2 |
26,328,583 (GRCm39) |
missense |
probably benign |
0.00 |
R6459:Sec16a
|
UTSW |
2 |
26,313,512 (GRCm39) |
missense |
probably benign |
0.04 |
R6520:Sec16a
|
UTSW |
2 |
26,316,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R6631:Sec16a
|
UTSW |
2 |
26,329,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R6657:Sec16a
|
UTSW |
2 |
26,315,876 (GRCm39) |
nonsense |
probably null |
|
R6750:Sec16a
|
UTSW |
2 |
26,330,030 (GRCm39) |
missense |
probably benign |
0.00 |
R6852:Sec16a
|
UTSW |
2 |
26,331,431 (GRCm39) |
missense |
probably damaging |
0.99 |
R6860:Sec16a
|
UTSW |
2 |
26,320,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R6967:Sec16a
|
UTSW |
2 |
26,320,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Sec16a
|
UTSW |
2 |
26,320,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6970:Sec16a
|
UTSW |
2 |
26,320,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6991:Sec16a
|
UTSW |
2 |
26,320,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6993:Sec16a
|
UTSW |
2 |
26,313,586 (GRCm39) |
missense |
probably damaging |
0.99 |
R7009:Sec16a
|
UTSW |
2 |
26,326,014 (GRCm39) |
nonsense |
probably null |
|
R7057:Sec16a
|
UTSW |
2 |
26,315,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R7186:Sec16a
|
UTSW |
2 |
26,330,715 (GRCm39) |
nonsense |
probably null |
|
R7227:Sec16a
|
UTSW |
2 |
26,328,935 (GRCm39) |
missense |
probably benign |
0.01 |
R7234:Sec16a
|
UTSW |
2 |
26,329,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R7259:Sec16a
|
UTSW |
2 |
26,331,604 (GRCm39) |
missense |
probably benign |
0.00 |
R7326:Sec16a
|
UTSW |
2 |
26,329,729 (GRCm39) |
missense |
unknown |
|
R7371:Sec16a
|
UTSW |
2 |
26,331,734 (GRCm39) |
missense |
probably benign |
|
R7388:Sec16a
|
UTSW |
2 |
26,318,376 (GRCm39) |
missense |
|
|
R7414:Sec16a
|
UTSW |
2 |
26,313,643 (GRCm39) |
missense |
|
|
R7417:Sec16a
|
UTSW |
2 |
26,311,409 (GRCm39) |
missense |
|
|
R7501:Sec16a
|
UTSW |
2 |
26,331,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R7558:Sec16a
|
UTSW |
2 |
26,329,746 (GRCm39) |
missense |
|
|
R7696:Sec16a
|
UTSW |
2 |
26,305,645 (GRCm39) |
critical splice donor site |
probably null |
|
R7981:Sec16a
|
UTSW |
2 |
26,311,384 (GRCm39) |
critical splice donor site |
probably null |
|
R8117:Sec16a
|
UTSW |
2 |
26,331,441 (GRCm39) |
missense |
probably benign |
0.00 |
R8131:Sec16a
|
UTSW |
2 |
26,300,958 (GRCm39) |
missense |
|
|
R8163:Sec16a
|
UTSW |
2 |
26,306,433 (GRCm39) |
missense |
|
|
R8825:Sec16a
|
UTSW |
2 |
26,313,586 (GRCm39) |
missense |
|
|
R8855:Sec16a
|
UTSW |
2 |
26,329,852 (GRCm39) |
missense |
probably benign |
0.16 |
R9165:Sec16a
|
UTSW |
2 |
26,313,645 (GRCm39) |
missense |
|
|
R9216:Sec16a
|
UTSW |
2 |
26,304,401 (GRCm39) |
missense |
|
|
R9283:Sec16a
|
UTSW |
2 |
26,313,904 (GRCm39) |
missense |
|
|
R9506:Sec16a
|
UTSW |
2 |
26,319,384 (GRCm39) |
critical splice donor site |
probably null |
|
R9581:Sec16a
|
UTSW |
2 |
26,328,647 (GRCm39) |
missense |
|
|
R9772:Sec16a
|
UTSW |
2 |
26,329,417 (GRCm39) |
missense |
possibly damaging |
0.87 |
X0011:Sec16a
|
UTSW |
2 |
26,305,655 (GRCm39) |
missense |
probably damaging |
1.00 |
X0034:Sec16a
|
UTSW |
2 |
26,306,709 (GRCm39) |
missense |
probably benign |
0.07 |
X0062:Sec16a
|
UTSW |
2 |
26,306,709 (GRCm39) |
missense |
probably benign |
0.07 |
Z1088:Sec16a
|
UTSW |
2 |
26,329,105 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Sec16a
|
UTSW |
2 |
26,328,760 (GRCm39) |
missense |
|
|
Z1177:Sec16a
|
UTSW |
2 |
26,329,333 (GRCm39) |
missense |
probably damaging |
0.99 |
|