Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810024B03Rik |
T |
G |
2: 127,028,710 (GRCm39) |
D163A |
possibly damaging |
Het |
Abce1 |
A |
T |
8: 80,414,537 (GRCm39) |
I454N |
probably damaging |
Het |
Acaca |
A |
G |
11: 84,262,339 (GRCm39) |
I1980M |
probably damaging |
Het |
Adgrb2 |
C |
T |
4: 129,885,917 (GRCm39) |
T19M |
probably benign |
Het |
Agmo |
T |
A |
12: 37,464,974 (GRCm39) |
S417T |
probably benign |
Het |
Akap8l |
T |
C |
17: 32,552,068 (GRCm39) |
E403G |
probably damaging |
Het |
Art5 |
C |
T |
7: 101,747,711 (GRCm39) |
A23T |
possibly damaging |
Het |
Atg9a |
T |
C |
1: 75,161,204 (GRCm39) |
T681A |
probably benign |
Het |
Atp11b |
A |
G |
3: 35,832,256 (GRCm39) |
Q37R |
probably damaging |
Het |
Atp2a2 |
T |
C |
5: 122,629,829 (GRCm39) |
E80G |
probably benign |
Het |
AW551984 |
G |
A |
9: 39,511,071 (GRCm39) |
P172L |
possibly damaging |
Het |
Bace1 |
C |
T |
9: 45,769,743 (GRCm39) |
R296C |
probably damaging |
Het |
Ccser1 |
T |
A |
6: 61,288,840 (GRCm39) |
H334Q |
probably benign |
Het |
Chtf18 |
C |
T |
17: 25,942,491 (GRCm39) |
R449H |
probably damaging |
Het |
Cit |
A |
G |
5: 116,122,881 (GRCm39) |
H1384R |
possibly damaging |
Het |
Cltc |
A |
G |
11: 86,612,474 (GRCm39) |
I524T |
probably benign |
Het |
Dctn1 |
T |
A |
6: 83,160,042 (GRCm39) |
I94N |
probably damaging |
Het |
Dnhd1 |
A |
T |
7: 105,354,472 (GRCm39) |
D3078V |
probably damaging |
Het |
Dock7 |
G |
A |
4: 98,943,683 (GRCm39) |
P520S |
|
Het |
Epb41l4a |
C |
A |
18: 33,987,326 (GRCm39) |
K350N |
probably damaging |
Het |
Eprs1 |
T |
A |
1: 185,145,366 (GRCm39) |
Y1130N |
probably damaging |
Het |
Fcgrt |
T |
C |
7: 44,744,797 (GRCm39) |
T224A |
probably damaging |
Het |
Flt1 |
T |
A |
5: 147,637,177 (GRCm39) |
T39S |
probably benign |
Het |
Fxyd1 |
T |
C |
7: 30,752,896 (GRCm39) |
Y33C |
probably damaging |
Het |
Gab2 |
T |
A |
7: 96,950,633 (GRCm39) |
V442E |
probably damaging |
Het |
Ganab |
A |
G |
19: 8,892,076 (GRCm39) |
D800G |
probably benign |
Het |
Gata4 |
C |
A |
14: 63,478,186 (GRCm39) |
A138S |
probably benign |
Het |
Golga4 |
A |
G |
9: 118,385,131 (GRCm39) |
H751R |
possibly damaging |
Het |
H1f6 |
A |
G |
13: 23,880,455 (GRCm39) |
R203G |
possibly damaging |
Het |
Htra4 |
A |
G |
8: 25,527,093 (GRCm39) |
V234A |
possibly damaging |
Het |
Igkv4-74 |
A |
T |
6: 69,161,954 (GRCm39) |
Y72N |
probably damaging |
Het |
Iqsec3 |
T |
C |
6: 121,360,940 (GRCm39) |
K973E |
probably damaging |
Het |
Khdc1b |
C |
A |
1: 21,455,065 (GRCm39) |
T108K |
probably benign |
Het |
Krtap5-1 |
ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG |
ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG |
7: 141,850,333 (GRCm39) |
|
probably benign |
Het |
Kyat3 |
A |
G |
3: 142,432,066 (GRCm39) |
|
probably null |
Het |
Lrba |
T |
A |
3: 86,225,474 (GRCm39) |
V666E |
probably damaging |
Het |
Mettl25 |
T |
A |
10: 105,601,871 (GRCm39) |
Y528F |
probably benign |
Het |
Mms19 |
A |
T |
19: 41,940,904 (GRCm39) |
Y619* |
probably null |
Het |
Nlrp12 |
A |
C |
7: 3,277,020 (GRCm39) |
|
probably null |
Het |
Nol10 |
C |
T |
12: 17,474,676 (GRCm39) |
L623F |
possibly damaging |
Het |
Oas1g |
A |
G |
5: 121,024,063 (GRCm39) |
F82S |
probably damaging |
Het |
Or1j8 |
T |
G |
2: 36,191,772 (GRCm39) |
S74A |
probably benign |
Het |
Or5k3 |
C |
T |
16: 58,969,570 (GRCm39) |
A119V |
probably damaging |
Het |
Or8g18 |
G |
A |
9: 39,149,546 (GRCm39) |
P58L |
probably benign |
Het |
Oxr1 |
G |
A |
15: 41,686,863 (GRCm39) |
E582K |
probably damaging |
Het |
Pdia3 |
A |
G |
2: 121,262,838 (GRCm39) |
D268G |
possibly damaging |
Het |
Pramel13 |
T |
C |
4: 144,119,434 (GRCm39) |
S378G |
probably damaging |
Het |
Rcor3 |
A |
G |
1: 191,786,078 (GRCm39) |
Y387H |
probably damaging |
Het |
Rigi |
T |
A |
4: 40,206,034 (GRCm39) |
I853F |
possibly damaging |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGGGGCGGCGG |
7: 97,229,118 (GRCm39) |
|
probably benign |
Het |
Rsl1 |
T |
C |
13: 67,330,284 (GRCm39) |
L244P |
possibly damaging |
Het |
Sdcbp |
C |
T |
4: 6,378,985 (GRCm39) |
A24V |
probably benign |
Het |
Slc22a8 |
A |
G |
19: 8,571,323 (GRCm39) |
Y18C |
possibly damaging |
Het |
Slc35d1 |
C |
T |
4: 103,072,044 (GRCm39) |
R7H |
probably damaging |
Het |
Slco6d1 |
A |
T |
1: 98,425,248 (GRCm39) |
T599S |
probably damaging |
Het |
Spata31d1e |
C |
T |
13: 59,889,437 (GRCm39) |
M794I |
not run |
Het |
St18 |
T |
A |
1: 6,872,761 (GRCm39) |
H165Q |
probably benign |
Het |
Sub1 |
C |
T |
15: 11,986,589 (GRCm39) |
R86K |
probably damaging |
Het |
Tectb |
G |
A |
19: 55,181,104 (GRCm39) |
V148M |
|
Het |
Tgfb2 |
C |
A |
1: 186,362,954 (GRCm39) |
G290V |
possibly damaging |
Het |
Tgm7 |
T |
C |
2: 120,924,191 (GRCm39) |
H577R |
probably benign |
Het |
Tle2 |
T |
C |
10: 81,422,981 (GRCm39) |
S460P |
probably damaging |
Het |
Tmem221 |
C |
A |
8: 72,011,446 (GRCm39) |
R3L |
possibly damaging |
Het |
Tnfrsf19 |
C |
A |
14: 61,212,183 (GRCm39) |
V156L |
possibly damaging |
Het |
Trav6-5 |
A |
G |
14: 53,728,964 (GRCm39) |
K75E |
probably benign |
Het |
Trip10 |
G |
A |
17: 57,569,442 (GRCm39) |
G488S |
probably damaging |
Het |
Usp34 |
A |
C |
11: 23,399,268 (GRCm39) |
K2419T |
|
Het |
Vps13d |
T |
C |
4: 144,801,622 (GRCm39) |
Q3532R |
|
Het |
Vps4a |
A |
T |
8: 107,767,529 (GRCm39) |
I163L |
probably damaging |
Het |
Wrn |
T |
C |
8: 33,814,454 (GRCm39) |
H330R |
probably benign |
Het |
Xpr1 |
T |
C |
1: 155,188,618 (GRCm39) |
I341V |
probably benign |
Het |
Zfyve9 |
T |
C |
4: 108,548,973 (GRCm39) |
E105G |
probably benign |
Het |
|
Other mutations in Scn5a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00336:Scn5a
|
APN |
9 |
119,315,290 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00480:Scn5a
|
APN |
9 |
119,346,604 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL00542:Scn5a
|
APN |
9 |
119,321,192 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00852:Scn5a
|
APN |
9 |
119,366,748 (GRCm39) |
missense |
probably benign |
0.26 |
IGL00895:Scn5a
|
APN |
9 |
119,342,170 (GRCm39) |
splice site |
probably null |
|
IGL00905:Scn5a
|
APN |
9 |
119,365,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01347:Scn5a
|
APN |
9 |
119,391,507 (GRCm39) |
nonsense |
probably null |
|
IGL01396:Scn5a
|
APN |
9 |
119,363,770 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01402:Scn5a
|
APN |
9 |
119,315,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01404:Scn5a
|
APN |
9 |
119,315,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01487:Scn5a
|
APN |
9 |
119,391,689 (GRCm39) |
start codon destroyed |
probably null |
0.90 |
IGL01612:Scn5a
|
APN |
9 |
119,315,091 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02134:Scn5a
|
APN |
9 |
119,314,958 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02434:Scn5a
|
APN |
9 |
119,362,859 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02698:Scn5a
|
APN |
9 |
119,350,163 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02717:Scn5a
|
APN |
9 |
119,358,076 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02746:Scn5a
|
APN |
9 |
119,379,703 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Scn5a
|
APN |
9 |
119,324,751 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03155:Scn5a
|
APN |
9 |
119,341,248 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL03188:Scn5a
|
APN |
9 |
119,351,632 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03268:Scn5a
|
APN |
9 |
119,350,297 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03287:Scn5a
|
APN |
9 |
119,318,844 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03328:Scn5a
|
APN |
9 |
119,366,702 (GRCm39) |
missense |
probably benign |
0.12 |
PIT4142001:Scn5a
|
UTSW |
9 |
119,315,324 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4520001:Scn5a
|
UTSW |
9 |
119,363,636 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0026:Scn5a
|
UTSW |
9 |
119,351,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R0044:Scn5a
|
UTSW |
9 |
119,321,113 (GRCm39) |
critical splice donor site |
probably null |
|
R0044:Scn5a
|
UTSW |
9 |
119,321,113 (GRCm39) |
critical splice donor site |
probably null |
|
R0267:Scn5a
|
UTSW |
9 |
119,372,201 (GRCm39) |
missense |
probably damaging |
0.98 |
R0313:Scn5a
|
UTSW |
9 |
119,363,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Scn5a
|
UTSW |
9 |
119,351,665 (GRCm39) |
missense |
probably damaging |
0.99 |
R0364:Scn5a
|
UTSW |
9 |
119,351,665 (GRCm39) |
missense |
probably damaging |
0.99 |
R0369:Scn5a
|
UTSW |
9 |
119,362,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R0512:Scn5a
|
UTSW |
9 |
119,379,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R0681:Scn5a
|
UTSW |
9 |
119,368,706 (GRCm39) |
missense |
probably damaging |
0.96 |
R1163:Scn5a
|
UTSW |
9 |
119,362,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Scn5a
|
UTSW |
9 |
119,362,727 (GRCm39) |
critical splice donor site |
probably null |
|
R1469:Scn5a
|
UTSW |
9 |
119,362,727 (GRCm39) |
critical splice donor site |
probably null |
|
R1470:Scn5a
|
UTSW |
9 |
119,365,541 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1470:Scn5a
|
UTSW |
9 |
119,365,541 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1530:Scn5a
|
UTSW |
9 |
119,324,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R1532:Scn5a
|
UTSW |
9 |
119,362,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R1544:Scn5a
|
UTSW |
9 |
119,315,699 (GRCm39) |
missense |
probably damaging |
1.00 |
R1588:Scn5a
|
UTSW |
9 |
119,350,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R1597:Scn5a
|
UTSW |
9 |
119,391,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R1607:Scn5a
|
UTSW |
9 |
119,315,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R1657:Scn5a
|
UTSW |
9 |
119,391,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R1664:Scn5a
|
UTSW |
9 |
119,350,243 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1785:Scn5a
|
UTSW |
9 |
119,350,195 (GRCm39) |
missense |
probably damaging |
1.00 |
R1925:Scn5a
|
UTSW |
9 |
119,358,085 (GRCm39) |
missense |
probably benign |
|
R1956:Scn5a
|
UTSW |
9 |
119,346,479 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2006:Scn5a
|
UTSW |
9 |
119,365,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Scn5a
|
UTSW |
9 |
119,314,717 (GRCm39) |
missense |
probably damaging |
0.98 |
R2083:Scn5a
|
UTSW |
9 |
119,321,189 (GRCm39) |
missense |
probably benign |
0.45 |
R2180:Scn5a
|
UTSW |
9 |
119,345,117 (GRCm39) |
missense |
probably benign |
|
R2216:Scn5a
|
UTSW |
9 |
119,342,151 (GRCm39) |
missense |
probably benign |
|
R2216:Scn5a
|
UTSW |
9 |
119,314,678 (GRCm39) |
missense |
probably benign |
0.37 |
R2320:Scn5a
|
UTSW |
9 |
119,359,022 (GRCm39) |
critical splice donor site |
probably null |
|
R2377:Scn5a
|
UTSW |
9 |
119,368,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R2510:Scn5a
|
UTSW |
9 |
119,362,751 (GRCm39) |
missense |
probably benign |
0.05 |
R3113:Scn5a
|
UTSW |
9 |
119,314,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R3769:Scn5a
|
UTSW |
9 |
119,381,142 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R4133:Scn5a
|
UTSW |
9 |
119,315,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R4164:Scn5a
|
UTSW |
9 |
119,324,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R4447:Scn5a
|
UTSW |
9 |
119,379,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R4635:Scn5a
|
UTSW |
9 |
119,358,051 (GRCm39) |
missense |
possibly damaging |
0.47 |
R4734:Scn5a
|
UTSW |
9 |
119,368,604 (GRCm39) |
missense |
probably damaging |
0.98 |
R4829:Scn5a
|
UTSW |
9 |
119,363,773 (GRCm39) |
missense |
probably benign |
0.00 |
R4867:Scn5a
|
UTSW |
9 |
119,379,737 (GRCm39) |
nonsense |
probably null |
|
R5055:Scn5a
|
UTSW |
9 |
119,351,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R5229:Scn5a
|
UTSW |
9 |
119,365,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R5344:Scn5a
|
UTSW |
9 |
119,363,073 (GRCm39) |
missense |
probably benign |
0.25 |
R5424:Scn5a
|
UTSW |
9 |
119,330,800 (GRCm39) |
missense |
probably damaging |
1.00 |
R5517:Scn5a
|
UTSW |
9 |
119,324,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R5526:Scn5a
|
UTSW |
9 |
119,350,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R5560:Scn5a
|
UTSW |
9 |
119,389,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R5719:Scn5a
|
UTSW |
9 |
119,359,118 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5726:Scn5a
|
UTSW |
9 |
119,362,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R5800:Scn5a
|
UTSW |
9 |
119,330,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R5826:Scn5a
|
UTSW |
9 |
119,350,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R6046:Scn5a
|
UTSW |
9 |
119,391,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R6101:Scn5a
|
UTSW |
9 |
119,351,716 (GRCm39) |
missense |
probably damaging |
0.98 |
R6162:Scn5a
|
UTSW |
9 |
119,351,621 (GRCm39) |
missense |
probably damaging |
0.98 |
R6375:Scn5a
|
UTSW |
9 |
119,372,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R6378:Scn5a
|
UTSW |
9 |
119,315,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R6464:Scn5a
|
UTSW |
9 |
119,363,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R6794:Scn5a
|
UTSW |
9 |
119,364,955 (GRCm39) |
missense |
probably damaging |
0.98 |
R6799:Scn5a
|
UTSW |
9 |
119,324,688 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6850:Scn5a
|
UTSW |
9 |
119,330,815 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6858:Scn5a
|
UTSW |
9 |
119,321,156 (GRCm39) |
missense |
probably benign |
0.11 |
R6861:Scn5a
|
UTSW |
9 |
119,359,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R6875:Scn5a
|
UTSW |
9 |
119,315,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R6989:Scn5a
|
UTSW |
9 |
119,315,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R7009:Scn5a
|
UTSW |
9 |
119,314,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R7064:Scn5a
|
UTSW |
9 |
119,318,977 (GRCm39) |
missense |
probably damaging |
0.99 |
R7145:Scn5a
|
UTSW |
9 |
119,315,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R7212:Scn5a
|
UTSW |
9 |
119,372,451 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7238:Scn5a
|
UTSW |
9 |
119,320,610 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7266:Scn5a
|
UTSW |
9 |
119,391,626 (GRCm39) |
missense |
probably benign |
0.37 |
R7348:Scn5a
|
UTSW |
9 |
119,364,899 (GRCm39) |
missense |
probably benign |
0.00 |
R7399:Scn5a
|
UTSW |
9 |
119,315,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R7453:Scn5a
|
UTSW |
9 |
119,351,656 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7495:Scn5a
|
UTSW |
9 |
119,372,200 (GRCm39) |
missense |
probably damaging |
0.99 |
R7681:Scn5a
|
UTSW |
9 |
119,359,043 (GRCm39) |
missense |
probably benign |
0.01 |
R7791:Scn5a
|
UTSW |
9 |
119,372,402 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7794:Scn5a
|
UTSW |
9 |
119,358,153 (GRCm39) |
missense |
probably damaging |
0.99 |
R7873:Scn5a
|
UTSW |
9 |
119,327,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R7951:Scn5a
|
UTSW |
9 |
119,358,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R8154:Scn5a
|
UTSW |
9 |
119,391,611 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8306:Scn5a
|
UTSW |
9 |
119,350,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R8329:Scn5a
|
UTSW |
9 |
119,365,030 (GRCm39) |
missense |
probably damaging |
0.96 |
R8390:Scn5a
|
UTSW |
9 |
119,368,604 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8536:Scn5a
|
UTSW |
9 |
119,368,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R8922:Scn5a
|
UTSW |
9 |
119,363,766 (GRCm39) |
missense |
probably benign |
|
R9000:Scn5a
|
UTSW |
9 |
119,321,171 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9015:Scn5a
|
UTSW |
9 |
119,381,142 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R9272:Scn5a
|
UTSW |
9 |
119,315,717 (GRCm39) |
missense |
probably damaging |
1.00 |
R9394:Scn5a
|
UTSW |
9 |
119,324,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R9448:Scn5a
|
UTSW |
9 |
119,381,127 (GRCm39) |
missense |
probably damaging |
0.99 |
R9511:Scn5a
|
UTSW |
9 |
119,351,611 (GRCm39) |
missense |
probably benign |
0.00 |
R9563:Scn5a
|
UTSW |
9 |
119,315,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R9593:Scn5a
|
UTSW |
9 |
119,315,839 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Scn5a
|
UTSW |
9 |
119,346,835 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Scn5a
|
UTSW |
9 |
119,314,735 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Scn5a
|
UTSW |
9 |
119,362,997 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Scn5a
|
UTSW |
9 |
119,351,584 (GRCm39) |
missense |
probably damaging |
1.00 |
|