Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
T |
A |
8: 41,207,671 (GRCm39) |
F312L |
probably benign |
Het |
Adprm |
A |
G |
11: 66,932,856 (GRCm39) |
F18L |
possibly damaging |
Het |
Ampd1 |
T |
G |
3: 103,006,981 (GRCm39) |
N735K |
possibly damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Atp1a4 |
T |
C |
1: 172,081,649 (GRCm39) |
M168V |
probably damaging |
Het |
Bcl6 |
G |
A |
16: 23,793,600 (GRCm39) |
H116Y |
probably damaging |
Het |
Bmpr2 |
T |
A |
1: 59,890,383 (GRCm39) |
N338K |
probably damaging |
Het |
Bms1 |
A |
T |
6: 118,381,224 (GRCm39) |
Y697* |
probably null |
Het |
Ccdc33 |
A |
C |
9: 58,025,918 (GRCm39) |
F37C |
probably damaging |
Het |
Ccdc60 |
T |
A |
5: 116,426,507 (GRCm39) |
Q30L |
probably benign |
Het |
Cndp1 |
C |
A |
18: 84,650,036 (GRCm39) |
R219L |
probably damaging |
Het |
Cstdc4 |
T |
C |
16: 36,006,837 (GRCm39) |
|
probably null |
Het |
Daam2 |
C |
A |
17: 49,783,550 (GRCm39) |
D627Y |
probably damaging |
Het |
Dffb |
T |
C |
4: 154,057,416 (GRCm39) |
D87G |
possibly damaging |
Het |
Dnah2 |
T |
G |
11: 69,388,708 (GRCm39) |
T892P |
possibly damaging |
Het |
Dqx1 |
A |
G |
6: 83,043,092 (GRCm39) |
T610A |
probably benign |
Het |
Dspp |
A |
T |
5: 104,324,926 (GRCm39) |
I430L |
possibly damaging |
Het |
Dytn |
T |
A |
1: 63,672,854 (GRCm39) |
K516N |
probably benign |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Fmnl2 |
T |
A |
2: 52,993,773 (GRCm39) |
N389K |
possibly damaging |
Het |
Fn1 |
G |
A |
1: 71,665,336 (GRCm39) |
T927I |
probably damaging |
Het |
Foxn1 |
T |
C |
11: 78,261,989 (GRCm39) |
K127E |
probably damaging |
Het |
Fpr-rs6 |
A |
G |
17: 20,402,608 (GRCm39) |
F251S |
probably damaging |
Het |
Frrs1 |
A |
G |
3: 116,672,088 (GRCm39) |
D62G |
probably damaging |
Het |
Fut10 |
T |
A |
8: 31,726,148 (GRCm39) |
V301D |
probably damaging |
Het |
Gk5 |
A |
G |
9: 96,059,470 (GRCm39) |
|
probably null |
Het |
Glipr1l1 |
T |
A |
10: 111,914,279 (GRCm39) |
N213K |
probably benign |
Het |
Gm1110 |
A |
G |
9: 26,793,162 (GRCm39) |
F538S |
probably benign |
Het |
Gm7347 |
T |
A |
5: 26,262,366 (GRCm39) |
T52S |
probably benign |
Het |
Gsap |
T |
C |
5: 21,427,406 (GRCm39) |
I178T |
probably damaging |
Het |
H1f9 |
C |
A |
11: 94,858,928 (GRCm39) |
N74K |
probably damaging |
Het |
Hcn1 |
A |
T |
13: 117,739,556 (GRCm39) |
Q106L |
unknown |
Het |
Isg20l2 |
G |
T |
3: 87,839,288 (GRCm39) |
L166F |
possibly damaging |
Het |
Kcnq3 |
T |
A |
15: 65,876,612 (GRCm39) |
E510D |
probably damaging |
Het |
Kif26b |
G |
T |
1: 178,755,895 (GRCm39) |
R2003L |
probably damaging |
Het |
Kiss1r |
T |
C |
10: 79,754,641 (GRCm39) |
V45A |
probably damaging |
Het |
Krt14 |
G |
A |
11: 100,098,032 (GRCm39) |
R84* |
probably null |
Het |
Mbd5 |
T |
C |
2: 49,148,208 (GRCm39) |
M806T |
possibly damaging |
Het |
Mdga1 |
A |
T |
17: 30,058,847 (GRCm39) |
I13N |
possibly damaging |
Het |
Mfsd4b5 |
T |
C |
10: 39,850,758 (GRCm39) |
K73E |
probably benign |
Het |
Mterf2 |
C |
T |
10: 84,955,596 (GRCm39) |
G343R |
probably benign |
Het |
Mto1 |
T |
A |
9: 78,368,903 (GRCm39) |
F522I |
probably benign |
Het |
Myo18b |
T |
C |
5: 112,937,923 (GRCm39) |
E1734G |
probably damaging |
Het |
Myoz1 |
T |
C |
14: 20,703,787 (GRCm39) |
T53A |
probably benign |
Het |
Naxd |
T |
C |
8: 11,563,032 (GRCm39) |
L324P |
probably damaging |
Het |
Nos1 |
T |
A |
5: 118,005,334 (GRCm39) |
V18D |
probably damaging |
Het |
Nova1 |
T |
C |
12: 46,863,738 (GRCm39) |
T71A |
unknown |
Het |
Or10v5 |
T |
C |
19: 11,805,482 (GRCm39) |
R303G |
probably benign |
Het |
Or10z1 |
A |
G |
1: 174,078,448 (GRCm39) |
L15S |
possibly damaging |
Het |
Or1e29 |
C |
G |
11: 73,668,007 (GRCm39) |
V49L |
probably benign |
Het |
Or2j6 |
T |
C |
7: 139,980,083 (GRCm39) |
D292G |
probably damaging |
Het |
Or52b1 |
A |
G |
7: 104,978,811 (GRCm39) |
V196A |
possibly damaging |
Het |
Otof |
T |
A |
5: 30,540,238 (GRCm39) |
Y981F |
probably damaging |
Het |
Peg10 |
C |
CTCA |
6: 4,756,453 (GRCm39) |
|
probably benign |
Het |
Pex1 |
A |
G |
5: 3,670,597 (GRCm39) |
K7E |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,120,946 (GRCm39) |
S73P |
possibly damaging |
Het |
Plxnb1 |
T |
A |
9: 108,929,498 (GRCm39) |
I118N |
possibly damaging |
Het |
Prcc |
T |
C |
3: 87,779,560 (GRCm39) |
D158G |
probably damaging |
Het |
Ptpn7 |
C |
A |
1: 135,066,877 (GRCm39) |
R245S |
possibly damaging |
Het |
Ptpre |
C |
T |
7: 135,270,861 (GRCm39) |
H346Y |
probably benign |
Het |
Pwp2 |
A |
G |
10: 78,018,527 (GRCm39) |
C86R |
probably benign |
Het |
Rfng |
T |
G |
11: 120,673,876 (GRCm39) |
D178A |
probably damaging |
Het |
Rhpn1 |
T |
C |
15: 75,580,090 (GRCm39) |
I51T |
probably damaging |
Het |
Rnasel |
G |
T |
1: 153,629,843 (GRCm39) |
E120* |
probably null |
Het |
Sall2 |
T |
G |
14: 52,553,112 (GRCm39) |
S26R |
possibly damaging |
Het |
Sdk2 |
C |
A |
11: 113,684,587 (GRCm39) |
R1958L |
probably damaging |
Het |
Septin4 |
C |
T |
11: 87,458,043 (GRCm39) |
S139F |
possibly damaging |
Het |
Slc52a2 |
T |
A |
15: 76,424,751 (GRCm39) |
C330S |
probably damaging |
Het |
Smarca2 |
T |
A |
19: 26,668,788 (GRCm39) |
I987N |
possibly damaging |
Het |
Srrt |
A |
T |
5: 137,294,271 (GRCm39) |
Y486N |
probably damaging |
Het |
Stat5b |
A |
T |
11: 100,695,831 (GRCm39) |
N50K |
possibly damaging |
Het |
Strip2 |
T |
A |
6: 29,931,265 (GRCm39) |
D405E |
probably benign |
Het |
Tcstv6 |
T |
A |
13: 120,298,474 (GRCm39) |
|
probably null |
Het |
Tnc |
A |
T |
4: 63,924,739 (GRCm39) |
D986E |
probably damaging |
Het |
Tph2 |
T |
C |
10: 114,915,621 (GRCm39) |
N473S |
probably benign |
Het |
Tpp1 |
C |
T |
7: 105,401,232 (GRCm39) |
|
probably benign |
Het |
Trpm3 |
T |
C |
19: 22,689,076 (GRCm39) |
Y2H |
probably damaging |
Het |
Ttc21a |
A |
T |
9: 119,795,195 (GRCm39) |
E1072V |
probably damaging |
Het |
Zfat |
T |
C |
15: 68,050,762 (GRCm39) |
D753G |
probably damaging |
Het |
Zmym2 |
T |
A |
14: 57,159,051 (GRCm39) |
S609T |
probably 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 |
|
R5193:Scn10a
|
UTSW |
9 |
119,438,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R5211:Scn10a
|
UTSW |
9 |
119,490,298 (GRCm39) |
missense |
possibly damaging |
0.87 |
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 |
|
|