Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930012K11Rik |
A |
G |
14: 70,394,233 (GRCm39) |
S181P |
probably benign |
Het |
Adgrf5 |
A |
T |
17: 43,733,511 (GRCm39) |
T112S |
probably benign |
Het |
Ascc2 |
T |
C |
11: 4,623,399 (GRCm39) |
V545A |
possibly damaging |
Het |
Bmp2 |
A |
T |
2: 133,396,550 (GRCm39) |
S69C |
probably damaging |
Het |
Btaf1 |
T |
A |
19: 36,973,962 (GRCm39) |
I1378K |
probably benign |
Het |
Ces2b |
C |
T |
8: 105,561,695 (GRCm39) |
T263I |
possibly damaging |
Het |
Cntn5 |
A |
T |
9: 9,704,894 (GRCm39) |
V635D |
possibly damaging |
Het |
Dock6 |
T |
C |
9: 21,731,648 (GRCm39) |
E1218G |
probably benign |
Het |
Eml6 |
T |
C |
11: 29,804,145 (GRCm39) |
I319V |
probably benign |
Het |
Esd |
T |
C |
14: 74,978,632 (GRCm39) |
S65P |
probably damaging |
Het |
Exoc1l |
C |
A |
5: 76,664,250 (GRCm39) |
T113K |
possibly damaging |
Het |
Fstl3 |
A |
T |
10: 79,616,012 (GRCm39) |
Q166L |
probably benign |
Het |
Garin1a |
A |
T |
6: 29,286,098 (GRCm39) |
K128* |
probably null |
Het |
Gcn1 |
T |
A |
5: 115,757,371 (GRCm39) |
S2445T |
probably benign |
Het |
Gfy |
C |
A |
7: 44,827,282 (GRCm39) |
L271F |
possibly damaging |
Het |
Gjc2 |
A |
G |
11: 59,068,284 (GRCm39) |
V66A |
possibly damaging |
Het |
H3c4 |
G |
T |
13: 23,760,015 (GRCm39) |
G14C |
possibly damaging |
Het |
Itm2c |
T |
A |
1: 85,834,249 (GRCm39) |
V188E |
probably damaging |
Het |
Jmjd1c |
C |
G |
10: 67,067,795 (GRCm39) |
S1766C |
probably damaging |
Het |
Kcnn3 |
A |
G |
3: 89,428,538 (GRCm39) |
T255A |
probably benign |
Het |
Kdm4d |
A |
C |
9: 14,374,400 (GRCm39) |
V486G |
probably benign |
Het |
Krt18 |
T |
G |
15: 101,939,888 (GRCm39) |
I362S |
probably damaging |
Het |
Lrrc8d |
G |
A |
5: 105,961,606 (GRCm39) |
R672Q |
probably damaging |
Het |
Ly6f |
G |
A |
15: 75,143,652 (GRCm39) |
V120M |
probably damaging |
Het |
Map3k4 |
A |
G |
17: 12,451,321 (GRCm39) |
V1524A |
possibly damaging |
Het |
Mrgprh |
T |
C |
17: 13,095,889 (GRCm39) |
V43A |
probably benign |
Het |
Mx2 |
A |
T |
16: 97,348,633 (GRCm39) |
M269L |
probably damaging |
Het |
Myrfl |
C |
T |
10: 116,634,535 (GRCm39) |
V620I |
probably benign |
Het |
Nlrp9b |
G |
A |
7: 19,783,381 (GRCm39) |
C908Y |
probably damaging |
Het |
Nyap2 |
T |
A |
1: 81,064,991 (GRCm39) |
M1K |
probably null |
Het |
Olfml3 |
A |
T |
3: 103,644,515 (GRCm39) |
H51Q |
probably benign |
Het |
Or11h6 |
C |
T |
14: 50,880,710 (GRCm39) |
T324I |
possibly damaging |
Het |
Pcdhb1 |
G |
A |
18: 37,399,704 (GRCm39) |
V552I |
probably benign |
Het |
Pm20d1 |
T |
A |
1: 131,734,647 (GRCm39) |
I353N |
possibly damaging |
Het |
Sbk2 |
A |
G |
7: 4,965,966 (GRCm39) |
F73L |
possibly damaging |
Het |
Slc45a2 |
C |
T |
15: 11,027,871 (GRCm39) |
T480I |
probably damaging |
Het |
Slmap |
T |
C |
14: 26,204,117 (GRCm39) |
Y68C |
probably damaging |
Het |
Syde2 |
T |
C |
3: 145,707,093 (GRCm39) |
V611A |
probably benign |
Het |
Sympk |
A |
G |
7: 18,769,814 (GRCm39) |
M164V |
probably benign |
Het |
Syt17 |
T |
C |
7: 118,041,626 (GRCm39) |
S43G |
probably benign |
Het |
Ubr1 |
T |
C |
2: 120,723,651 (GRCm39) |
T1303A |
possibly damaging |
Het |
Vmn2r100 |
A |
G |
17: 19,746,257 (GRCm39) |
Y535C |
possibly damaging |
Het |
|
Other mutations in Scn10a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Scn10a
|
APN |
9 |
119,501,292 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01339:Scn10a
|
APN |
9 |
119,451,832 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01467:Scn10a
|
APN |
9 |
119,487,478 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01472:Scn10a
|
APN |
9 |
119,446,829 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01481:Scn10a
|
APN |
9 |
119,438,260 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01539:Scn10a
|
APN |
9 |
119,467,764 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01580:Scn10a
|
APN |
9 |
119,456,225 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01676:Scn10a
|
APN |
9 |
119,501,231 (GRCm39) |
nonsense |
probably null |
|
IGL01681:Scn10a
|
APN |
9 |
119,523,143 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01748:Scn10a
|
APN |
9 |
119,456,150 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01866:Scn10a
|
APN |
9 |
119,464,568 (GRCm39) |
nonsense |
probably null |
|
IGL01998:Scn10a
|
APN |
9 |
119,438,742 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02015:Scn10a
|
APN |
9 |
119,494,017 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02098:Scn10a
|
APN |
9 |
119,520,544 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02113:Scn10a
|
APN |
9 |
119,438,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02245:Scn10a
|
APN |
9 |
119,501,218 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02262:Scn10a
|
APN |
9 |
119,487,499 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02317:Scn10a
|
APN |
9 |
119,467,621 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02428:Scn10a
|
APN |
9 |
119,520,628 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02439:Scn10a
|
APN |
9 |
119,447,914 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02583:Scn10a
|
APN |
9 |
119,520,506 (GRCm39) |
splice site |
probably benign |
|
IGL02597:Scn10a
|
APN |
9 |
119,439,189 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02680:Scn10a
|
APN |
9 |
119,495,125 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02733:Scn10a
|
APN |
9 |
119,445,771 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Scn10a
|
APN |
9 |
119,500,674 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02992:Scn10a
|
APN |
9 |
119,438,626 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03040:Scn10a
|
APN |
9 |
119,452,051 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03049:Scn10a
|
APN |
9 |
119,495,056 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03407:Scn10a
|
APN |
9 |
119,477,237 (GRCm39) |
missense |
probably damaging |
0.99 |
possum
|
UTSW |
9 |
119,467,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R0025:Scn10a
|
UTSW |
9 |
119,499,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R0030:Scn10a
|
UTSW |
9 |
119,499,056 (GRCm39) |
missense |
probably benign |
0.01 |
R0328:Scn10a
|
UTSW |
9 |
119,523,168 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0494:Scn10a
|
UTSW |
9 |
119,453,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R0511:Scn10a
|
UTSW |
9 |
119,442,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R0548:Scn10a
|
UTSW |
9 |
119,494,994 (GRCm39) |
missense |
probably benign |
0.00 |
R0584:Scn10a
|
UTSW |
9 |
119,499,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R0595:Scn10a
|
UTSW |
9 |
119,495,129 (GRCm39) |
missense |
probably benign |
0.01 |
R0894:Scn10a
|
UTSW |
9 |
119,459,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R1022:Scn10a
|
UTSW |
9 |
119,438,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R1024:Scn10a
|
UTSW |
9 |
119,438,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R1263:Scn10a
|
UTSW |
9 |
119,446,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R1456:Scn10a
|
UTSW |
9 |
119,520,544 (GRCm39) |
missense |
probably benign |
0.01 |
R1466:Scn10a
|
UTSW |
9 |
119,495,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Scn10a
|
UTSW |
9 |
119,495,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R1573:Scn10a
|
UTSW |
9 |
119,442,692 (GRCm39) |
missense |
probably benign |
0.04 |
R1704:Scn10a
|
UTSW |
9 |
119,438,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R1933:Scn10a
|
UTSW |
9 |
119,439,064 (GRCm39) |
missense |
probably damaging |
1.00 |
R1945:Scn10a
|
UTSW |
9 |
119,520,520 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2013:Scn10a
|
UTSW |
9 |
119,442,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R2155:Scn10a
|
UTSW |
9 |
119,438,514 (GRCm39) |
missense |
probably benign |
0.02 |
R2196:Scn10a
|
UTSW |
9 |
119,438,070 (GRCm39) |
missense |
probably benign |
|
R2231:Scn10a
|
UTSW |
9 |
119,462,916 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2353:Scn10a
|
UTSW |
9 |
119,467,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R2392:Scn10a
|
UTSW |
9 |
119,456,268 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2895:Scn10a
|
UTSW |
9 |
119,490,467 (GRCm39) |
missense |
probably benign |
0.00 |
R2926:Scn10a
|
UTSW |
9 |
119,467,767 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3783:Scn10a
|
UTSW |
9 |
119,520,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R3821:Scn10a
|
UTSW |
9 |
119,467,699 (GRCm39) |
missense |
probably benign |
|
R4003:Scn10a
|
UTSW |
9 |
119,438,034 (GRCm39) |
missense |
probably null |
0.00 |
R4208:Scn10a
|
UTSW |
9 |
119,445,842 (GRCm39) |
missense |
probably damaging |
0.99 |
R4231:Scn10a
|
UTSW |
9 |
119,460,610 (GRCm39) |
missense |
probably damaging |
0.98 |
R4626:Scn10a
|
UTSW |
9 |
119,460,571 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4702:Scn10a
|
UTSW |
9 |
119,462,857 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4713:Scn10a
|
UTSW |
9 |
119,438,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R4729:Scn10a
|
UTSW |
9 |
119,500,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R4782:Scn10a
|
UTSW |
9 |
119,451,976 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4822:Scn10a
|
UTSW |
9 |
119,467,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R4856:Scn10a
|
UTSW |
9 |
119,523,376 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4856:Scn10a
|
UTSW |
9 |
119,523,375 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4932:Scn10a
|
UTSW |
9 |
119,516,940 (GRCm39) |
splice site |
probably null |
|
R5015:Scn10a
|
UTSW |
9 |
119,451,987 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5193:Scn10a
|
UTSW |
9 |
119,438,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R5320:Scn10a
|
UTSW |
9 |
119,477,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R5400:Scn10a
|
UTSW |
9 |
119,438,100 (GRCm39) |
missense |
probably damaging |
0.99 |
R5448:Scn10a
|
UTSW |
9 |
119,517,013 (GRCm39) |
missense |
probably benign |
0.25 |
R5457:Scn10a
|
UTSW |
9 |
119,523,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R5554:Scn10a
|
UTSW |
9 |
119,523,196 (GRCm39) |
missense |
probably benign |
0.01 |
R5680:Scn10a
|
UTSW |
9 |
119,453,202 (GRCm39) |
missense |
probably damaging |
1.00 |
R5762:Scn10a
|
UTSW |
9 |
119,464,507 (GRCm39) |
critical splice donor site |
probably null |
|
R5935:Scn10a
|
UTSW |
9 |
119,456,237 (GRCm39) |
missense |
probably damaging |
0.99 |
R5956:Scn10a
|
UTSW |
9 |
119,460,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R6041:Scn10a
|
UTSW |
9 |
119,438,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R6047:Scn10a
|
UTSW |
9 |
119,451,897 (GRCm39) |
missense |
probably benign |
0.20 |
R6132:Scn10a
|
UTSW |
9 |
119,442,761 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6156:Scn10a
|
UTSW |
9 |
119,464,649 (GRCm39) |
missense |
probably benign |
0.00 |
R6309:Scn10a
|
UTSW |
9 |
119,453,181 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6318:Scn10a
|
UTSW |
9 |
119,456,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R6394:Scn10a
|
UTSW |
9 |
119,490,386 (GRCm39) |
missense |
probably benign |
0.36 |
R6711:Scn10a
|
UTSW |
9 |
119,438,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R6751:Scn10a
|
UTSW |
9 |
119,500,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R6877:Scn10a
|
UTSW |
9 |
119,438,848 (GRCm39) |
missense |
probably damaging |
0.96 |
R6909:Scn10a
|
UTSW |
9 |
119,438,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R7023:Scn10a
|
UTSW |
9 |
119,442,610 (GRCm39) |
missense |
probably damaging |
0.99 |
R7205:Scn10a
|
UTSW |
9 |
119,442,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R7254:Scn10a
|
UTSW |
9 |
119,447,921 (GRCm39) |
missense |
probably damaging |
0.99 |
R7261:Scn10a
|
UTSW |
9 |
119,438,790 (GRCm39) |
missense |
probably damaging |
0.97 |
R7283:Scn10a
|
UTSW |
9 |
119,493,845 (GRCm39) |
critical splice donor site |
probably null |
|
R7453:Scn10a
|
UTSW |
9 |
119,467,618 (GRCm39) |
missense |
probably benign |
|
R7561:Scn10a
|
UTSW |
9 |
119,523,390 (GRCm39) |
start codon destroyed |
probably null |
0.66 |
R7590:Scn10a
|
UTSW |
9 |
119,495,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R7759:Scn10a
|
UTSW |
9 |
119,477,198 (GRCm39) |
nonsense |
probably null |
|
R7765:Scn10a
|
UTSW |
9 |
119,438,970 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7851:Scn10a
|
UTSW |
9 |
119,446,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R7875:Scn10a
|
UTSW |
9 |
119,464,508 (GRCm39) |
critical splice donor site |
probably null |
|
R7975:Scn10a
|
UTSW |
9 |
119,501,286 (GRCm39) |
missense |
probably benign |
0.31 |
R8010:Scn10a
|
UTSW |
9 |
119,490,233 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8027:Scn10a
|
UTSW |
9 |
119,462,856 (GRCm39) |
missense |
probably damaging |
0.99 |
R8221:Scn10a
|
UTSW |
9 |
119,446,829 (GRCm39) |
missense |
probably damaging |
1.00 |
R8249:Scn10a
|
UTSW |
9 |
119,446,840 (GRCm39) |
missense |
probably damaging |
1.00 |
R8319:Scn10a
|
UTSW |
9 |
119,499,455 (GRCm39) |
missense |
probably benign |
0.04 |
R8323:Scn10a
|
UTSW |
9 |
119,438,462 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8539:Scn10a
|
UTSW |
9 |
119,467,840 (GRCm39) |
nonsense |
probably null |
|
R8679:Scn10a
|
UTSW |
9 |
119,501,194 (GRCm39) |
missense |
probably damaging |
0.97 |
R8680:Scn10a
|
UTSW |
9 |
119,520,509 (GRCm39) |
critical splice donor site |
probably null |
|
R8844:Scn10a
|
UTSW |
9 |
119,446,791 (GRCm39) |
missense |
probably damaging |
0.98 |
R9011:Scn10a
|
UTSW |
9 |
119,459,160 (GRCm39) |
missense |
probably damaging |
0.99 |
R9055:Scn10a
|
UTSW |
9 |
119,451,958 (GRCm39) |
missense |
probably damaging |
0.98 |
R9206:Scn10a
|
UTSW |
9 |
119,445,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R9615:Scn10a
|
UTSW |
9 |
119,487,504 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9622:Scn10a
|
UTSW |
9 |
119,438,046 (GRCm39) |
missense |
probably benign |
0.11 |
R9641:Scn10a
|
UTSW |
9 |
119,445,869 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9651:Scn10a
|
UTSW |
9 |
119,439,063 (GRCm39) |
missense |
probably benign |
0.17 |
X0058:Scn10a
|
UTSW |
9 |
119,438,430 (GRCm39) |
nonsense |
probably null |
|
Z1177:Scn10a
|
UTSW |
9 |
119,453,211 (GRCm39) |
critical splice acceptor site |
probably null |
|
|