Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd17a |
A |
G |
10: 80,419,737 (GRCm39) |
Y290H |
probably benign |
Het |
Aco2 |
T |
C |
15: 81,788,142 (GRCm39) |
V257A |
probably damaging |
Het |
Adam26a |
C |
A |
8: 44,023,007 (GRCm39) |
C161F |
possibly damaging |
Het |
Adam9 |
G |
A |
8: 25,445,988 (GRCm39) |
P820S |
unknown |
Het |
Adcy4 |
G |
A |
14: 56,010,922 (GRCm39) |
T665M |
probably benign |
Het |
Ahnak |
T |
A |
19: 8,984,188 (GRCm39) |
M1824K |
probably benign |
Het |
Alpi |
T |
C |
1: 87,026,795 (GRCm39) |
N428D |
probably benign |
Het |
Ano5 |
C |
T |
7: 51,196,528 (GRCm39) |
P153L |
probably benign |
Het |
Atp1a1 |
A |
T |
3: 101,489,437 (GRCm39) |
L725* |
probably null |
Het |
Atp8b2 |
G |
A |
3: 89,854,071 (GRCm39) |
T595I |
probably damaging |
Het |
Ccdc66 |
T |
C |
14: 27,220,820 (GRCm39) |
I35V |
possibly damaging |
Het |
Cd163 |
A |
G |
6: 124,284,187 (GRCm39) |
T120A |
probably benign |
Het |
Cmah |
A |
T |
13: 24,640,938 (GRCm39) |
T396S |
possibly damaging |
Het |
Cmya5 |
C |
T |
13: 93,205,820 (GRCm39) |
V3350I |
probably benign |
Het |
Commd9 |
A |
C |
2: 101,731,410 (GRCm39) |
K198N |
probably damaging |
Het |
Cxcr1 |
A |
G |
1: 74,231,773 (GRCm39) |
V83A |
probably benign |
Het |
D630045J12Rik |
A |
G |
6: 38,125,383 (GRCm39) |
S1544P |
probably damaging |
Het |
Ddt |
A |
T |
10: 75,609,048 (GRCm39) |
|
probably null |
Het |
Depdc7 |
A |
G |
2: 104,557,585 (GRCm39) |
S222P |
possibly damaging |
Het |
Ehd2 |
A |
G |
7: 15,684,431 (GRCm39) |
I456T |
probably damaging |
Het |
Epas1 |
A |
T |
17: 87,136,471 (GRCm39) |
M748L |
probably benign |
Het |
Esr1 |
G |
A |
10: 4,806,903 (GRCm39) |
R273H |
probably damaging |
Het |
Fras1 |
G |
A |
5: 96,916,297 (GRCm39) |
D3444N |
probably damaging |
Het |
Hand2 |
A |
G |
8: 57,775,272 (GRCm39) |
R111G |
probably damaging |
Het |
Ift140 |
T |
C |
17: 25,252,089 (GRCm39) |
I312T |
probably benign |
Het |
Ikbke |
A |
T |
1: 131,199,887 (GRCm39) |
L257* |
probably null |
Het |
Kcnk5 |
G |
A |
14: 20,192,349 (GRCm39) |
P271S |
probably benign |
Het |
Lama1 |
T |
C |
17: 68,044,662 (GRCm39) |
V187A |
|
Het |
Lemd2 |
A |
T |
17: 27,412,810 (GRCm39) |
|
probably null |
Het |
Lig3 |
T |
A |
11: 82,679,717 (GRCm39) |
D341E |
probably benign |
Het |
Lpcat1 |
C |
T |
13: 73,643,014 (GRCm39) |
S196L |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 40,567,582 (GRCm39) |
D4048E |
|
Het |
Lrrfip1 |
G |
A |
1: 91,033,005 (GRCm39) |
E158K |
probably damaging |
Het |
Mcm5 |
T |
C |
8: 75,848,220 (GRCm39) |
S490P |
probably damaging |
Het |
Mia3 |
A |
C |
1: 183,147,036 (GRCm39) |
Y73* |
probably null |
Het |
Minar1 |
T |
A |
9: 89,483,888 (GRCm39) |
H503L |
probably benign |
Het |
Msr1 |
A |
T |
8: 40,077,003 (GRCm39) |
N202K |
probably benign |
Het |
N4bp2l2 |
A |
T |
5: 150,585,286 (GRCm39) |
Y231* |
probably null |
Het |
Nbeal2 |
A |
G |
9: 110,482,985 (GRCm39) |
W11R |
probably benign |
Het |
Ncor1 |
T |
C |
11: 62,264,250 (GRCm39) |
E384G |
possibly damaging |
Het |
Neb |
A |
G |
2: 52,137,202 (GRCm39) |
V254A |
|
Het |
Nlrp9b |
T |
C |
7: 19,779,691 (GRCm39) |
S785P |
probably benign |
Het |
Oprd1 |
T |
G |
4: 131,841,092 (GRCm39) |
I289L |
possibly damaging |
Het |
Or4c10 |
G |
T |
2: 89,761,064 (GRCm39) |
D304Y |
probably benign |
Het |
Or4s2 |
A |
G |
2: 88,473,752 (GRCm39) |
I214V |
probably benign |
Het |
Or5m12 |
A |
G |
2: 85,734,447 (GRCm39) |
V317A |
probably benign |
Het |
Or6a2 |
T |
C |
7: 106,600,534 (GRCm39) |
T178A |
probably benign |
Het |
Or6c2 |
T |
A |
10: 129,362,429 (GRCm39) |
F111Y |
possibly damaging |
Het |
Orc1 |
A |
G |
4: 108,445,951 (GRCm39) |
N23S |
probably benign |
Het |
Paip1 |
A |
T |
13: 119,577,356 (GRCm39) |
H149L |
possibly damaging |
Het |
Pdhx |
A |
T |
2: 102,877,099 (GRCm39) |
D103E |
probably benign |
Het |
Pi4ka |
T |
C |
16: 17,109,080 (GRCm39) |
Y1614C |
|
Het |
Pias3 |
ACC |
AC |
3: 96,608,701 (GRCm39) |
|
probably null |
Het |
Pigb |
A |
G |
9: 72,941,770 (GRCm39) |
V163A |
probably benign |
Het |
Pla2g4d |
A |
G |
2: 120,114,620 (GRCm39) |
I37T |
possibly damaging |
Het |
Ppfia1 |
A |
T |
7: 144,059,982 (GRCm39) |
V610D |
probably damaging |
Het |
Pramel41 |
G |
A |
5: 94,596,394 (GRCm39) |
C477Y |
probably damaging |
Het |
Prss1 |
T |
C |
6: 41,439,507 (GRCm39) |
V80A |
probably benign |
Het |
Psph |
G |
A |
5: 129,847,800 (GRCm39) |
R49W |
probably benign |
Het |
Qrich2 |
T |
C |
11: 116,347,080 (GRCm39) |
Y1248C |
possibly damaging |
Het |
Rlbp1 |
T |
A |
7: 79,029,861 (GRCm39) |
Y124F |
probably damaging |
Het |
Scn4a |
T |
A |
11: 106,239,995 (GRCm39) |
E74V |
probably benign |
Het |
Sdk2 |
A |
T |
11: 113,764,039 (GRCm39) |
I249N |
possibly damaging |
Het |
Sgsh |
A |
T |
11: 119,237,378 (GRCm39) |
L412Q |
probably damaging |
Het |
Shank1 |
C |
A |
7: 44,002,452 (GRCm39) |
D1390E |
probably benign |
Het |
Slc12a6 |
A |
G |
2: 112,172,319 (GRCm39) |
D421G |
probably damaging |
Het |
Snx29 |
T |
A |
16: 11,238,649 (GRCm39) |
|
probably null |
Het |
Spata31d1c |
A |
G |
13: 65,183,937 (GRCm39) |
Y493C |
probably damaging |
Het |
Stmn4 |
G |
A |
14: 66,593,727 (GRCm39) |
G40E |
probably damaging |
Het |
Stox2 |
A |
G |
8: 47,656,154 (GRCm39) |
|
probably null |
Het |
Strada |
T |
C |
11: 106,077,830 (GRCm39) |
S45G |
unknown |
Het |
Taco1 |
G |
A |
11: 105,962,774 (GRCm39) |
G154S |
probably benign |
Het |
Tas2r121 |
T |
C |
6: 132,677,505 (GRCm39) |
M156V |
probably benign |
Het |
Tbc1d31 |
A |
G |
15: 57,804,136 (GRCm39) |
S384G |
probably benign |
Het |
Tbc1d9 |
A |
T |
8: 83,966,560 (GRCm39) |
D387V |
probably damaging |
Het |
Tet3 |
A |
G |
6: 83,345,289 (GRCm39) |
L1716P |
probably damaging |
Het |
Thbs1 |
A |
G |
2: 117,943,843 (GRCm39) |
K154E |
possibly damaging |
Het |
Ush2a |
T |
C |
1: 187,999,241 (GRCm39) |
Y184H |
possibly damaging |
Het |
Vmn1r235 |
C |
A |
17: 21,481,713 (GRCm39) |
Q13K |
probably benign |
Het |
Vmn2r15 |
A |
T |
5: 109,440,774 (GRCm39) |
Y361* |
probably null |
Het |
Vmn2r88 |
A |
T |
14: 51,648,315 (GRCm39) |
|
probably null |
Het |
Vps54 |
T |
C |
11: 21,248,831 (GRCm39) |
V460A |
probably benign |
Het |
Wdr64 |
A |
G |
1: 175,613,147 (GRCm39) |
N674S |
possibly damaging |
Het |
Zfp592 |
A |
G |
7: 80,673,390 (GRCm39) |
D118G |
probably benign |
Het |
Zfp763 |
A |
G |
17: 33,237,625 (GRCm39) |
Y507H |
probably benign |
Het |
Zfp934 |
T |
C |
13: 62,640,705 (GRCm39) |
E16G |
probably damaging |
Het |
Zfyve26 |
G |
A |
12: 79,337,731 (GRCm39) |
L94F |
probably damaging |
Het |
|
Other mutations in Hecw1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00591:Hecw1
|
APN |
13 |
14,440,565 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL00813:Hecw1
|
APN |
13 |
14,452,961 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL00843:Hecw1
|
APN |
13 |
14,422,158 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00942:Hecw1
|
APN |
13 |
14,515,325 (GRCm39) |
splice site |
probably benign |
|
IGL00976:Hecw1
|
APN |
13 |
14,493,557 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01289:Hecw1
|
APN |
13 |
14,438,719 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01675:Hecw1
|
APN |
13 |
14,409,007 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01783:Hecw1
|
APN |
13 |
14,452,878 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01941:Hecw1
|
APN |
13 |
14,490,895 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02170:Hecw1
|
APN |
13 |
14,438,743 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02172:Hecw1
|
APN |
13 |
14,438,734 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02214:Hecw1
|
APN |
13 |
14,474,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02350:Hecw1
|
APN |
13 |
14,422,923 (GRCm39) |
splice site |
probably null |
|
IGL02357:Hecw1
|
APN |
13 |
14,422,923 (GRCm39) |
splice site |
probably null |
|
IGL02372:Hecw1
|
APN |
13 |
14,438,706 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02591:Hecw1
|
APN |
13 |
14,531,821 (GRCm39) |
splice site |
probably benign |
|
IGL02718:Hecw1
|
APN |
13 |
14,481,520 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02795:Hecw1
|
APN |
13 |
14,497,102 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02941:Hecw1
|
APN |
13 |
14,552,311 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03256:Hecw1
|
APN |
13 |
14,455,070 (GRCm39) |
missense |
probably benign |
0.36 |
IGL03256:Hecw1
|
APN |
13 |
14,455,069 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03366:Hecw1
|
APN |
13 |
14,552,382 (GRCm39) |
missense |
probably damaging |
1.00 |
deflated
|
UTSW |
13 |
14,422,205 (GRCm39) |
missense |
possibly damaging |
0.69 |
Demoralized
|
UTSW |
13 |
14,491,403 (GRCm39) |
nonsense |
probably null |
|
Letdown
|
UTSW |
13 |
14,491,077 (GRCm39) |
missense |
probably benign |
0.40 |
BB001:Hecw1
|
UTSW |
13 |
14,497,113 (GRCm39) |
missense |
probably damaging |
1.00 |
BB011:Hecw1
|
UTSW |
13 |
14,497,113 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03014:Hecw1
|
UTSW |
13 |
14,420,393 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4378001:Hecw1
|
UTSW |
13 |
14,552,368 (GRCm39) |
missense |
probably damaging |
0.98 |
R0555:Hecw1
|
UTSW |
13 |
14,411,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Hecw1
|
UTSW |
13 |
14,455,027 (GRCm39) |
missense |
probably benign |
0.44 |
R1476:Hecw1
|
UTSW |
13 |
14,480,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R1479:Hecw1
|
UTSW |
13 |
14,491,077 (GRCm39) |
missense |
probably benign |
0.40 |
R1551:Hecw1
|
UTSW |
13 |
14,491,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R1579:Hecw1
|
UTSW |
13 |
14,552,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R1584:Hecw1
|
UTSW |
13 |
14,515,328 (GRCm39) |
critical splice donor site |
probably null |
|
R1735:Hecw1
|
UTSW |
13 |
14,552,350 (GRCm39) |
missense |
probably null |
0.09 |
R1872:Hecw1
|
UTSW |
13 |
14,455,034 (GRCm39) |
nonsense |
probably null |
|
R1897:Hecw1
|
UTSW |
13 |
14,552,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R2054:Hecw1
|
UTSW |
13 |
14,471,998 (GRCm39) |
missense |
probably damaging |
0.97 |
R2085:Hecw1
|
UTSW |
13 |
14,438,672 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2134:Hecw1
|
UTSW |
13 |
14,552,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R2172:Hecw1
|
UTSW |
13 |
14,552,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R2258:Hecw1
|
UTSW |
13 |
14,490,723 (GRCm39) |
missense |
probably benign |
0.01 |
R2274:Hecw1
|
UTSW |
13 |
14,520,653 (GRCm39) |
missense |
probably benign |
0.00 |
R2275:Hecw1
|
UTSW |
13 |
14,520,653 (GRCm39) |
missense |
probably benign |
0.00 |
R2937:Hecw1
|
UTSW |
13 |
14,420,421 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3830:Hecw1
|
UTSW |
13 |
14,520,643 (GRCm39) |
missense |
probably benign |
0.13 |
R3971:Hecw1
|
UTSW |
13 |
14,411,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R4065:Hecw1
|
UTSW |
13 |
14,491,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R4066:Hecw1
|
UTSW |
13 |
14,491,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R4235:Hecw1
|
UTSW |
13 |
14,491,724 (GRCm39) |
missense |
probably benign |
0.42 |
R4366:Hecw1
|
UTSW |
13 |
14,490,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4382:Hecw1
|
UTSW |
13 |
14,490,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4385:Hecw1
|
UTSW |
13 |
14,490,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4510:Hecw1
|
UTSW |
13 |
14,531,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R4511:Hecw1
|
UTSW |
13 |
14,531,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R4558:Hecw1
|
UTSW |
13 |
14,422,190 (GRCm39) |
missense |
probably damaging |
0.99 |
R4804:Hecw1
|
UTSW |
13 |
14,480,570 (GRCm39) |
missense |
probably benign |
0.00 |
R4854:Hecw1
|
UTSW |
13 |
14,491,477 (GRCm39) |
missense |
probably benign |
0.00 |
R5104:Hecw1
|
UTSW |
13 |
14,515,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R5113:Hecw1
|
UTSW |
13 |
14,520,614 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5167:Hecw1
|
UTSW |
13 |
14,460,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R5392:Hecw1
|
UTSW |
13 |
14,420,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R5394:Hecw1
|
UTSW |
13 |
14,497,174 (GRCm39) |
missense |
probably damaging |
1.00 |
R5504:Hecw1
|
UTSW |
13 |
14,515,487 (GRCm39) |
missense |
probably benign |
0.04 |
R5764:Hecw1
|
UTSW |
13 |
14,497,094 (GRCm39) |
missense |
probably damaging |
1.00 |
R6038:Hecw1
|
UTSW |
13 |
14,520,647 (GRCm39) |
missense |
probably benign |
0.28 |
R6038:Hecw1
|
UTSW |
13 |
14,520,647 (GRCm39) |
missense |
probably benign |
0.28 |
R6228:Hecw1
|
UTSW |
13 |
14,520,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Hecw1
|
UTSW |
13 |
14,409,010 (GRCm39) |
nonsense |
probably null |
|
R6252:Hecw1
|
UTSW |
13 |
14,446,664 (GRCm39) |
missense |
probably damaging |
0.98 |
R6291:Hecw1
|
UTSW |
13 |
14,697,592 (GRCm39) |
unclassified |
probably benign |
|
R6321:Hecw1
|
UTSW |
13 |
14,697,414 (GRCm39) |
missense |
probably benign |
0.00 |
R6325:Hecw1
|
UTSW |
13 |
14,491,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R6328:Hecw1
|
UTSW |
13 |
14,422,205 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6557:Hecw1
|
UTSW |
13 |
14,491,231 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6566:Hecw1
|
UTSW |
13 |
14,471,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R6597:Hecw1
|
UTSW |
13 |
14,491,403 (GRCm39) |
nonsense |
probably null |
|
R6821:Hecw1
|
UTSW |
13 |
14,438,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R6914:Hecw1
|
UTSW |
13 |
14,491,423 (GRCm39) |
missense |
probably damaging |
0.99 |
R7078:Hecw1
|
UTSW |
13 |
14,609,044 (GRCm39) |
start codon destroyed |
probably null |
0.21 |
R7114:Hecw1
|
UTSW |
13 |
14,486,356 (GRCm39) |
missense |
probably benign |
0.02 |
R7140:Hecw1
|
UTSW |
13 |
14,491,118 (GRCm39) |
missense |
probably benign |
|
R7150:Hecw1
|
UTSW |
13 |
14,609,045 (GRCm39) |
start codon destroyed |
probably benign |
|
R7288:Hecw1
|
UTSW |
13 |
14,490,821 (GRCm39) |
missense |
probably benign |
0.00 |
R7447:Hecw1
|
UTSW |
13 |
14,531,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R7479:Hecw1
|
UTSW |
13 |
14,515,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R7590:Hecw1
|
UTSW |
13 |
14,438,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R7787:Hecw1
|
UTSW |
13 |
14,493,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R7803:Hecw1
|
UTSW |
13 |
14,408,927 (GRCm39) |
missense |
probably benign |
0.25 |
R7924:Hecw1
|
UTSW |
13 |
14,497,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R7967:Hecw1
|
UTSW |
13 |
14,552,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R8176:Hecw1
|
UTSW |
13 |
14,422,286 (GRCm39) |
splice site |
probably null |
|
R8195:Hecw1
|
UTSW |
13 |
14,480,692 (GRCm39) |
missense |
probably damaging |
0.99 |
R8252:Hecw1
|
UTSW |
13 |
14,515,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R8696:Hecw1
|
UTSW |
13 |
14,531,743 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8827:Hecw1
|
UTSW |
13 |
14,438,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R8867:Hecw1
|
UTSW |
13 |
14,422,275 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8914:Hecw1
|
UTSW |
13 |
14,422,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R8942:Hecw1
|
UTSW |
13 |
14,481,395 (GRCm39) |
missense |
probably benign |
0.28 |
R9126:Hecw1
|
UTSW |
13 |
14,546,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R9185:Hecw1
|
UTSW |
13 |
14,491,628 (GRCm39) |
missense |
probably damaging |
0.99 |
R9203:Hecw1
|
UTSW |
13 |
14,491,243 (GRCm39) |
missense |
probably benign |
0.00 |
R9236:Hecw1
|
UTSW |
13 |
14,490,643 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9291:Hecw1
|
UTSW |
13 |
14,491,522 (GRCm39) |
missense |
probably benign |
|
R9312:Hecw1
|
UTSW |
13 |
14,546,567 (GRCm39) |
missense |
probably damaging |
0.99 |
R9438:Hecw1
|
UTSW |
13 |
14,481,414 (GRCm39) |
missense |
probably benign |
0.00 |
R9502:Hecw1
|
UTSW |
13 |
14,546,567 (GRCm39) |
missense |
probably damaging |
0.97 |
R9642:Hecw1
|
UTSW |
13 |
14,515,394 (GRCm39) |
missense |
probably damaging |
1.00 |
RF001:Hecw1
|
UTSW |
13 |
14,472,009 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Hecw1
|
UTSW |
13 |
14,405,308 (GRCm39) |
missense |
possibly damaging |
0.52 |
X0066:Hecw1
|
UTSW |
13 |
14,455,045 (GRCm39) |
missense |
probably benign |
0.13 |
Z1176:Hecw1
|
UTSW |
13 |
14,474,918 (GRCm39) |
missense |
possibly damaging |
0.77 |
|