Incidental Mutation 'R4732:Dnah12'
ID |
359101 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Dnah12
|
Ensembl Gene |
ENSMUSG00000021879 |
Gene Name |
dynein, axonemal, heavy chain 12 |
Synonyms |
HL19, DHC3, Dnahc7l, 4921531P07Rik, HL-19, LOC380889, Hdhc3, Dnahc12, DLP12 |
MMRRC Submission |
042022-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.187)
|
Stock # |
R4732 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
14 |
Chromosomal Location |
26414429-26613660 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 26503741 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Isoleucine
at position 1653
(T1653I)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000022433
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022433]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000022433
AA Change: T1653I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000022433 Gene: ENSMUSG00000021879 AA Change: T1653I
Domain | Start | End | E-Value | Type |
low complexity region
|
127 |
140 |
N/A |
INTRINSIC |
coiled coil region
|
588 |
666 |
N/A |
INTRINSIC |
Pfam:DHC_N2
|
676 |
1113 |
1.1e-147 |
PFAM |
AAA
|
1268 |
1407 |
1.15e0 |
SMART |
Pfam:AAA_5
|
1552 |
1695 |
1.5e-7 |
PFAM |
Blast:AAA
|
1709 |
1827 |
2e-24 |
BLAST |
Blast:AAA
|
1848 |
1898 |
1e-16 |
BLAST |
AAA
|
1903 |
2051 |
5.42e-4 |
SMART |
Pfam:AAA_8
|
2238 |
2316 |
2e-18 |
PFAM |
|
Meta Mutation Damage Score |
0.1735 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.2%
- 20x: 95.1%
|
Validation Efficiency |
99% (110/111) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 192 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700128F08Rik |
T |
A |
9: 8,222,174 (GRCm39) |
|
noncoding transcript |
Het |
4933409G03Rik |
A |
G |
2: 68,445,065 (GRCm39) |
|
probably benign |
Het |
Acan |
T |
C |
7: 78,748,357 (GRCm39) |
S1043P |
probably damaging |
Het |
Ackr2 |
A |
G |
9: 121,738,249 (GRCm39) |
Y208C |
probably damaging |
Het |
Actg1 |
C |
T |
11: 120,238,305 (GRCm39) |
|
probably benign |
Het |
Actmap |
T |
A |
7: 26,900,468 (GRCm39) |
M149K |
probably damaging |
Het |
Adam1a |
T |
A |
5: 121,657,497 (GRCm39) |
T599S |
probably benign |
Het |
Adamts12 |
A |
T |
15: 11,270,748 (GRCm39) |
S668C |
probably damaging |
Het |
Adcy8 |
A |
G |
15: 64,626,711 (GRCm39) |
V709A |
possibly damaging |
Het |
Adgrf2 |
A |
C |
17: 43,021,645 (GRCm39) |
I393S |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,984,665 (GRCm39) |
G1983V |
probably damaging |
Het |
Aim2 |
T |
A |
1: 173,291,442 (GRCm39) |
D282E |
possibly damaging |
Het |
Ak8 |
A |
G |
2: 28,650,083 (GRCm39) |
Y370C |
probably damaging |
Het |
Akap9 |
A |
G |
5: 4,063,901 (GRCm39) |
D1750G |
probably damaging |
Het |
Als2cl |
T |
A |
9: 110,718,204 (GRCm39) |
V315E |
probably damaging |
Het |
Ankrd28 |
A |
C |
14: 31,477,698 (GRCm39) |
C115G |
probably benign |
Het |
Ap3b2 |
C |
T |
7: 81,121,680 (GRCm39) |
A519T |
probably damaging |
Het |
Apool |
C |
T |
X: 111,281,897 (GRCm39) |
T166I |
probably damaging |
Het |
Arhgef2 |
A |
T |
3: 88,539,247 (GRCm39) |
K65* |
probably null |
Het |
Arhgef38 |
G |
T |
3: 132,838,030 (GRCm39) |
Y633* |
probably null |
Het |
Asah2 |
T |
C |
19: 31,972,758 (GRCm39) |
N659S |
probably benign |
Het |
Atf7ip2 |
A |
G |
16: 10,059,750 (GRCm39) |
D430G |
possibly damaging |
Het |
Atp8a1 |
G |
A |
5: 67,970,463 (GRCm39) |
S92L |
probably benign |
Het |
Bag4 |
C |
T |
8: 26,259,516 (GRCm39) |
A228T |
probably benign |
Het |
C130073F10Rik |
C |
A |
4: 101,747,907 (GRCm39) |
S89I |
probably benign |
Het |
Cacna1g |
T |
C |
11: 94,334,041 (GRCm39) |
T867A |
probably damaging |
Het |
Ccdc88a |
T |
G |
11: 29,435,906 (GRCm39) |
N1276K |
probably benign |
Het |
Cdc42bpg |
T |
A |
19: 6,361,221 (GRCm39) |
V282E |
probably damaging |
Het |
Cdipt |
T |
A |
7: 126,577,530 (GRCm39) |
L92H |
probably damaging |
Het |
Celsr2 |
T |
A |
3: 108,306,268 (GRCm39) |
D2012V |
probably damaging |
Het |
Cenpt |
A |
G |
8: 106,573,768 (GRCm39) |
V254A |
probably benign |
Het |
Cep104 |
T |
A |
4: 154,072,883 (GRCm39) |
D380E |
probably damaging |
Het |
Cers5 |
C |
T |
15: 99,639,518 (GRCm39) |
R123Q |
probably benign |
Het |
Ces2h |
A |
G |
8: 105,741,236 (GRCm39) |
E76G |
probably damaging |
Het |
Cfap77 |
T |
A |
2: 28,874,400 (GRCm39) |
E143D |
probably benign |
Het |
Chmp7 |
C |
A |
14: 69,969,745 (GRCm39) |
R65L |
probably damaging |
Het |
Cldnd2 |
T |
A |
7: 43,091,613 (GRCm39) |
C65S |
possibly damaging |
Het |
Clec2g |
C |
A |
6: 128,958,842 (GRCm39) |
Y142* |
probably null |
Het |
Coch |
A |
T |
12: 51,651,802 (GRCm39) |
E549V |
probably benign |
Het |
Cog7 |
T |
C |
7: 121,563,467 (GRCm39) |
D215G |
probably benign |
Het |
Col4a2 |
T |
C |
8: 11,464,779 (GRCm39) |
V348A |
probably benign |
Het |
Col4a2 |
A |
G |
8: 11,496,197 (GRCm39) |
H1606R |
probably benign |
Het |
Cpd |
T |
C |
11: 76,702,620 (GRCm39) |
N583D |
probably damaging |
Het |
Cyp2d11 |
T |
A |
15: 82,273,428 (GRCm39) |
Y481F |
probably benign |
Het |
D130043K22Rik |
T |
C |
13: 25,083,648 (GRCm39) |
S1038P |
probably damaging |
Het |
Deptor |
C |
A |
15: 55,044,406 (GRCm39) |
H191N |
probably benign |
Het |
Dgkz |
A |
T |
2: 91,768,684 (GRCm39) |
I699N |
probably damaging |
Het |
Dnah7c |
T |
A |
1: 46,809,333 (GRCm39) |
N3550K |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,994,035 (GRCm39) |
K3384R |
probably null |
Het |
Dnajc11 |
A |
G |
4: 152,055,424 (GRCm39) |
|
probably benign |
Het |
Dnajc13 |
CT |
C |
9: 104,064,004 (GRCm39) |
|
probably benign |
Het |
Dnhd1 |
C |
A |
7: 105,323,056 (GRCm39) |
N521K |
probably benign |
Het |
Drg2 |
T |
C |
11: 60,352,222 (GRCm39) |
|
probably null |
Het |
Dync1h1 |
C |
T |
12: 110,615,941 (GRCm39) |
Q3030* |
probably null |
Het |
Efhb |
G |
A |
17: 53,733,272 (GRCm39) |
T533I |
probably damaging |
Het |
Eif2d |
T |
C |
1: 131,092,464 (GRCm39) |
V374A |
probably damaging |
Het |
Etfb |
T |
C |
7: 43,093,624 (GRCm39) |
V17A |
probably damaging |
Het |
F5 |
C |
T |
1: 164,009,226 (GRCm39) |
T332M |
probably damaging |
Het |
Fcho1 |
T |
C |
8: 72,169,439 (GRCm39) |
T156A |
probably benign |
Het |
Fn1 |
A |
T |
1: 71,641,671 (GRCm39) |
|
probably null |
Het |
Fnip2 |
A |
T |
3: 79,388,959 (GRCm39) |
S561T |
probably damaging |
Het |
Frs2 |
T |
A |
10: 116,909,998 (GRCm39) |
T455S |
probably benign |
Het |
Fry |
G |
A |
5: 150,309,472 (GRCm39) |
E639K |
|
Het |
Fto |
T |
A |
8: 92,136,342 (GRCm39) |
D205E |
probably damaging |
Het |
Galnt2l |
A |
G |
8: 122,997,013 (GRCm39) |
|
probably benign |
Het |
Galntl6 |
G |
A |
8: 58,880,847 (GRCm39) |
P147L |
probably damaging |
Het |
Gigyf1 |
T |
A |
5: 137,523,032 (GRCm39) |
D844E |
probably benign |
Het |
Gle1 |
T |
C |
2: 29,830,244 (GRCm39) |
S267P |
probably damaging |
Het |
Glg1 |
G |
A |
8: 111,914,387 (GRCm39) |
R466W |
probably damaging |
Het |
Gm10277 |
T |
C |
11: 77,676,923 (GRCm39) |
|
probably benign |
Het |
Gm6871 |
T |
C |
7: 41,196,173 (GRCm39) |
I39V |
probably benign |
Het |
Gm9970 |
A |
G |
5: 31,398,410 (GRCm39) |
|
probably benign |
Het |
Gpr35 |
T |
G |
1: 92,911,107 (GRCm39) |
I57S |
probably damaging |
Het |
Gprin1 |
C |
T |
13: 54,887,770 (GRCm39) |
G168E |
possibly damaging |
Het |
Gtdc1 |
A |
G |
2: 44,679,067 (GRCm39) |
|
probably benign |
Het |
Gtf3c2 |
G |
T |
5: 31,317,401 (GRCm39) |
P586T |
probably damaging |
Het |
Gucy1a2 |
A |
T |
9: 3,759,424 (GRCm39) |
H410L |
probably benign |
Het |
Gucy2c |
A |
G |
6: 136,744,150 (GRCm39) |
S150P |
probably damaging |
Het |
Ifi214 |
T |
C |
1: 173,354,157 (GRCm39) |
Q171R |
probably benign |
Het |
Ifit1bl1 |
T |
C |
19: 34,571,721 (GRCm39) |
I245M |
probably benign |
Het |
Igkv4-50 |
T |
C |
6: 69,677,984 (GRCm39) |
K40R |
probably benign |
Het |
Igkv8-18 |
T |
A |
6: 70,333,280 (GRCm39) |
I74N |
probably damaging |
Het |
Il2ra |
T |
A |
2: 11,681,731 (GRCm39) |
M112K |
probably benign |
Het |
Itpr2 |
A |
G |
6: 146,274,671 (GRCm39) |
F837S |
probably damaging |
Het |
Kbtbd7 |
T |
C |
14: 79,666,240 (GRCm39) |
*691Q |
probably null |
Het |
Kcnn2 |
T |
A |
18: 45,693,416 (GRCm39) |
S331T |
possibly damaging |
Het |
Khnyn |
T |
A |
14: 56,123,946 (GRCm39) |
|
probably null |
Het |
Kif26a |
G |
A |
12: 112,142,007 (GRCm39) |
A754T |
probably benign |
Het |
Klra3 |
T |
A |
6: 130,304,095 (GRCm39) |
Y199F |
possibly damaging |
Het |
Lhx2 |
A |
G |
2: 38,250,003 (GRCm39) |
K274R |
probably damaging |
Het |
Lrp2 |
T |
C |
2: 69,363,899 (GRCm39) |
I313V |
probably benign |
Het |
Lrrfip1 |
A |
T |
1: 91,043,369 (GRCm39) |
E591D |
probably benign |
Het |
Lrrk2 |
G |
A |
15: 91,649,950 (GRCm39) |
E1696K |
probably damaging |
Het |
Lrrk2 |
A |
C |
15: 91,573,052 (GRCm39) |
E200A |
probably damaging |
Het |
Mast4 |
A |
T |
13: 102,909,080 (GRCm39) |
M465K |
probably damaging |
Het |
Moxd2 |
T |
G |
6: 40,855,793 (GRCm39) |
I599L |
probably benign |
Het |
Mug2 |
T |
C |
6: 122,048,831 (GRCm39) |
S866P |
probably damaging |
Het |
Ncam2 |
A |
G |
16: 81,231,772 (GRCm39) |
T79A |
possibly damaging |
Het |
Ncoa6 |
C |
A |
2: 155,263,221 (GRCm39) |
Q404H |
probably damaging |
Het |
Neb |
A |
G |
2: 52,169,091 (GRCm39) |
Y1815H |
probably damaging |
Het |
Nell1 |
A |
G |
7: 50,505,965 (GRCm39) |
D724G |
probably damaging |
Het |
Nkx3-2 |
A |
G |
5: 41,919,487 (GRCm39) |
V167A |
probably benign |
Het |
Nsun3 |
C |
A |
16: 62,555,482 (GRCm39) |
C348F |
possibly damaging |
Het |
Obox6 |
A |
T |
7: 15,568,697 (GRCm39) |
S60T |
possibly damaging |
Het |
Oog2 |
T |
A |
4: 143,920,511 (GRCm39) |
|
probably benign |
Het |
Or10g9b |
A |
T |
9: 39,917,564 (GRCm39) |
I227N |
probably damaging |
Het |
Or11g2 |
T |
A |
14: 50,856,026 (GRCm39) |
C116S |
probably benign |
Het |
Or1ad6 |
G |
A |
11: 50,860,093 (GRCm39) |
V83M |
possibly damaging |
Het |
Or1e16 |
T |
C |
11: 73,286,521 (GRCm39) |
D109G |
probably benign |
Het |
Or2i1 |
T |
C |
17: 37,507,915 (GRCm39) |
T315A |
probably damaging |
Het |
Or2n1e |
T |
A |
17: 38,586,438 (GRCm39) |
Y259N |
probably damaging |
Het |
Or9s18 |
T |
C |
13: 65,300,467 (GRCm39) |
V143A |
possibly damaging |
Het |
Pabpc1 |
A |
T |
15: 36,599,528 (GRCm39) |
V389E |
probably benign |
Het |
Pank4 |
A |
T |
4: 155,055,847 (GRCm39) |
M291L |
probably benign |
Het |
Pcf11 |
T |
C |
7: 92,308,041 (GRCm39) |
D709G |
probably benign |
Het |
Pcgf1 |
T |
A |
6: 83,056,938 (GRCm39) |
|
probably benign |
Het |
Pcnx1 |
A |
G |
12: 82,042,525 (GRCm39) |
I2256V |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,033,214 (GRCm39) |
D579G |
probably benign |
Het |
Pex6 |
A |
G |
17: 47,035,633 (GRCm39) |
|
probably null |
Het |
Piezo2 |
C |
T |
18: 63,163,472 (GRCm39) |
A2149T |
probably damaging |
Het |
Pik3c2g |
A |
G |
6: 139,881,711 (GRCm39) |
E781G |
probably benign |
Het |
Pik3r4 |
G |
A |
9: 105,555,375 (GRCm39) |
V1111I |
possibly damaging |
Het |
Pkd1l2 |
T |
A |
8: 117,722,581 (GRCm39) |
|
probably null |
Het |
Plekhg1 |
T |
A |
10: 3,907,506 (GRCm39) |
S808T |
probably benign |
Het |
Pnkp |
T |
A |
7: 44,509,878 (GRCm39) |
|
probably benign |
Het |
Polr3c |
A |
T |
3: 96,630,977 (GRCm39) |
F148I |
probably damaging |
Het |
Ppard |
A |
T |
17: 28,505,417 (GRCm39) |
T35S |
probably benign |
Het |
Ptov1 |
T |
C |
7: 44,516,533 (GRCm39) |
D134G |
probably benign |
Het |
Ptprz1 |
T |
A |
6: 23,002,609 (GRCm39) |
S1566R |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,445,504 (GRCm39) |
S158P |
probably benign |
Het |
Qki |
T |
C |
17: 10,435,217 (GRCm39) |
H269R |
probably damaging |
Het |
Qrsl1 |
T |
C |
10: 43,752,659 (GRCm39) |
Y388C |
probably damaging |
Het |
Rapgef1 |
T |
G |
2: 29,579,172 (GRCm39) |
I182S |
probably damaging |
Het |
Ret |
T |
C |
6: 118,140,154 (GRCm39) |
S1013G |
possibly damaging |
Het |
Rimbp3 |
A |
G |
16: 17,028,465 (GRCm39) |
R630G |
possibly damaging |
Het |
Rnmt |
A |
T |
18: 68,451,031 (GRCm39) |
|
probably benign |
Het |
Ryr2 |
A |
T |
13: 11,592,795 (GRCm39) |
M4653K |
possibly damaging |
Het |
Sacm1l |
G |
A |
9: 123,419,895 (GRCm39) |
V553I |
probably benign |
Het |
Sec31b |
A |
T |
19: 44,521,116 (GRCm39) |
S110T |
probably damaging |
Het |
Serpina3k |
G |
A |
12: 104,307,119 (GRCm39) |
G117D |
probably damaging |
Het |
Sesn2 |
T |
C |
4: 132,221,902 (GRCm39) |
Y410C |
probably damaging |
Het |
Slc24a1 |
G |
A |
9: 64,856,836 (GRCm39) |
R24C |
probably benign |
Het |
Slc35g2 |
A |
C |
9: 100,434,555 (GRCm39) |
V372G |
probably benign |
Het |
Slc7a7 |
T |
C |
14: 54,646,190 (GRCm39) |
Y91C |
probably damaging |
Het |
Slc7a9 |
T |
A |
7: 35,152,988 (GRCm39) |
Y135* |
probably null |
Het |
Slco1a7 |
A |
T |
6: 141,668,905 (GRCm39) |
M509K |
probably benign |
Het |
Slco4a1 |
A |
G |
2: 180,115,408 (GRCm39) |
N662D |
probably damaging |
Het |
Slfn4 |
T |
A |
11: 83,080,108 (GRCm39) |
|
probably benign |
Het |
Slmap |
T |
C |
14: 26,189,690 (GRCm39) |
N156S |
probably damaging |
Het |
Smim29 |
A |
G |
17: 27,784,244 (GRCm39) |
|
probably benign |
Het |
Snx18 |
A |
G |
13: 113,754,310 (GRCm39) |
S208P |
probably benign |
Het |
Sorbs1 |
T |
A |
19: 40,303,133 (GRCm39) |
R485S |
probably benign |
Het |
Spib |
A |
G |
7: 44,178,309 (GRCm39) |
S154P |
probably damaging |
Het |
Spty2d1 |
T |
C |
7: 46,645,858 (GRCm39) |
D595G |
probably damaging |
Het |
St7 |
T |
A |
6: 17,906,515 (GRCm39) |
|
probably null |
Het |
Susd1 |
T |
C |
4: 59,428,029 (GRCm39) |
T52A |
possibly damaging |
Het |
Svs5 |
T |
A |
2: 164,079,043 (GRCm39) |
D288V |
possibly damaging |
Het |
Syt7 |
T |
A |
19: 10,420,288 (GRCm39) |
I355N |
probably damaging |
Het |
Tarm1 |
G |
A |
7: 3,545,416 (GRCm39) |
Q145* |
probably null |
Het |
Teddm2 |
T |
A |
1: 153,726,487 (GRCm39) |
E76V |
probably damaging |
Het |
Thsd7b |
T |
C |
1: 129,540,923 (GRCm39) |
S343P |
probably damaging |
Het |
Tigd2 |
T |
A |
6: 59,188,400 (GRCm39) |
H422Q |
probably benign |
Het |
Tle1 |
T |
C |
4: 72,043,256 (GRCm39) |
N538D |
possibly damaging |
Het |
Tmc2 |
A |
G |
2: 130,103,317 (GRCm39) |
|
probably null |
Het |
Tmtc1 |
A |
C |
6: 148,186,478 (GRCm39) |
|
probably null |
Het |
Tns3 |
C |
T |
11: 8,400,986 (GRCm39) |
R1104H |
probably benign |
Het |
Trim6 |
T |
C |
7: 103,881,855 (GRCm39) |
Y369H |
probably damaging |
Het |
Triobp |
G |
A |
15: 78,851,313 (GRCm39) |
R489K |
probably damaging |
Het |
Trpv4 |
T |
C |
5: 114,760,814 (GRCm39) |
D732G |
possibly damaging |
Het |
Trrap |
G |
A |
5: 144,753,380 (GRCm39) |
V1883I |
probably damaging |
Het |
Tsc2 |
C |
A |
17: 24,822,249 (GRCm39) |
V1141F |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,730,171 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,773,355 (GRCm39) |
M2395K |
unknown |
Het |
Tyrp1 |
A |
T |
4: 80,763,172 (GRCm39) |
D353V |
possibly damaging |
Het |
Ubd |
A |
C |
17: 37,506,593 (GRCm39) |
T160P |
probably benign |
Het |
Ugt2b36 |
G |
T |
5: 87,229,397 (GRCm39) |
Y156* |
probably null |
Het |
Ulk4 |
G |
A |
9: 121,092,704 (GRCm39) |
R178* |
probably null |
Het |
Unc13d |
A |
G |
11: 115,964,408 (GRCm39) |
V312A |
possibly damaging |
Het |
Urb2 |
G |
T |
8: 124,755,636 (GRCm39) |
A448S |
probably damaging |
Het |
Urod |
G |
A |
4: 116,848,870 (GRCm39) |
A92V |
possibly damaging |
Het |
Vmn1r33 |
T |
A |
6: 66,588,803 (GRCm39) |
R250S |
probably benign |
Het |
Vmn1r87 |
A |
T |
7: 12,866,254 (GRCm39) |
M11K |
possibly damaging |
Het |
Vmn2r77 |
C |
T |
7: 86,450,195 (GRCm39) |
T147I |
probably benign |
Het |
Vstm4 |
A |
G |
14: 32,639,859 (GRCm39) |
K96E |
possibly damaging |
Het |
Vxn |
T |
C |
1: 9,677,201 (GRCm39) |
S24P |
probably benign |
Het |
Washc4 |
A |
T |
10: 83,410,343 (GRCm39) |
M644L |
probably benign |
Het |
Wwp1 |
T |
C |
4: 19,661,990 (GRCm39) |
D172G |
probably benign |
Het |
Zbtb38 |
A |
T |
9: 96,569,737 (GRCm39) |
V449E |
probably damaging |
Het |
Zfhx4 |
T |
C |
3: 5,279,867 (GRCm39) |
|
probably benign |
Het |
Zfp229 |
C |
T |
17: 21,964,267 (GRCm39) |
H166Y |
possibly damaging |
Het |
Zfp512b |
A |
G |
2: 181,230,532 (GRCm39) |
S453P |
probably benign |
Het |
Zp2 |
C |
A |
7: 119,737,343 (GRCm39) |
V282L |
probably damaging |
Het |
|
Other mutations in Dnah12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01412:Dnah12
|
APN |
14 |
26,492,962 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01602:Dnah12
|
APN |
14 |
26,431,430 (GRCm39) |
splice site |
probably benign |
|
IGL01681:Dnah12
|
APN |
14 |
26,443,315 (GRCm39) |
missense |
probably benign |
|
IGL02082:Dnah12
|
APN |
14 |
26,428,317 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02140:Dnah12
|
APN |
14 |
26,437,732 (GRCm39) |
missense |
probably benign |
0.20 |
IGL02170:Dnah12
|
APN |
14 |
26,495,069 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02174:Dnah12
|
APN |
14 |
26,428,072 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02367:Dnah12
|
APN |
14 |
26,430,316 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02418:Dnah12
|
APN |
14 |
26,495,679 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03039:Dnah12
|
APN |
14 |
26,445,667 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03066:Dnah12
|
APN |
14 |
26,418,553 (GRCm39) |
missense |
probably benign |
0.06 |
drippings
|
UTSW |
14 |
26,576,761 (GRCm39) |
missense |
probably damaging |
1.00 |
grueben
|
UTSW |
14 |
26,600,036 (GRCm39) |
missense |
probably damaging |
1.00 |
BB010:Dnah12
|
UTSW |
14 |
26,488,072 (GRCm39) |
missense |
probably benign |
0.00 |
BB020:Dnah12
|
UTSW |
14 |
26,488,072 (GRCm39) |
missense |
probably benign |
0.00 |
F5770:Dnah12
|
UTSW |
14 |
26,495,050 (GRCm39) |
missense |
possibly damaging |
0.95 |
FR4304:Dnah12
|
UTSW |
14 |
26,571,342 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4340:Dnah12
|
UTSW |
14 |
26,571,342 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4342:Dnah12
|
UTSW |
14 |
26,571,342 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4589:Dnah12
|
UTSW |
14 |
26,571,342 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03055:Dnah12
|
UTSW |
14 |
26,594,697 (GRCm39) |
missense |
probably damaging |
1.00 |
LCD18:Dnah12
|
UTSW |
14 |
26,571,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R0003:Dnah12
|
UTSW |
14 |
26,494,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Dnah12
|
UTSW |
14 |
26,520,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R0302:Dnah12
|
UTSW |
14 |
26,521,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R0355:Dnah12
|
UTSW |
14 |
26,427,272 (GRCm39) |
splice site |
probably null |
|
R0364:Dnah12
|
UTSW |
14 |
26,445,628 (GRCm39) |
missense |
probably benign |
0.10 |
R0469:Dnah12
|
UTSW |
14 |
26,520,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R0558:Dnah12
|
UTSW |
14 |
26,430,465 (GRCm39) |
missense |
probably benign |
0.00 |
R0709:Dnah12
|
UTSW |
14 |
26,606,222 (GRCm39) |
splice site |
probably benign |
|
R0734:Dnah12
|
UTSW |
14 |
26,521,970 (GRCm39) |
missense |
probably benign |
0.00 |
R1273:Dnah12
|
UTSW |
14 |
26,460,375 (GRCm39) |
nonsense |
probably null |
|
R1496:Dnah12
|
UTSW |
14 |
26,431,403 (GRCm39) |
missense |
probably benign |
|
R1503:Dnah12
|
UTSW |
14 |
26,495,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R1535:Dnah12
|
UTSW |
14 |
26,538,279 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1608:Dnah12
|
UTSW |
14 |
26,488,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R1682:Dnah12
|
UTSW |
14 |
26,500,840 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1758:Dnah12
|
UTSW |
14 |
26,488,071 (GRCm39) |
missense |
probably benign |
0.02 |
R1826:Dnah12
|
UTSW |
14 |
26,432,174 (GRCm39) |
missense |
probably benign |
0.01 |
R1829:Dnah12
|
UTSW |
14 |
26,522,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R1829:Dnah12
|
UTSW |
14 |
26,494,980 (GRCm39) |
missense |
probably damaging |
1.00 |
R1862:Dnah12
|
UTSW |
14 |
26,430,412 (GRCm39) |
missense |
probably benign |
0.30 |
R1862:Dnah12
|
UTSW |
14 |
26,418,553 (GRCm39) |
missense |
probably benign |
0.06 |
R1913:Dnah12
|
UTSW |
14 |
26,514,221 (GRCm39) |
splice site |
probably null |
|
R1933:Dnah12
|
UTSW |
14 |
26,455,650 (GRCm39) |
missense |
probably damaging |
0.98 |
R2006:Dnah12
|
UTSW |
14 |
26,536,416 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2045:Dnah12
|
UTSW |
14 |
26,503,485 (GRCm39) |
missense |
probably null |
1.00 |
R2113:Dnah12
|
UTSW |
14 |
26,488,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Dnah12
|
UTSW |
14 |
26,445,613 (GRCm39) |
nonsense |
probably null |
|
R2126:Dnah12
|
UTSW |
14 |
26,445,613 (GRCm39) |
nonsense |
probably null |
|
R2207:Dnah12
|
UTSW |
14 |
26,503,744 (GRCm39) |
missense |
probably damaging |
0.99 |
R2213:Dnah12
|
UTSW |
14 |
26,460,485 (GRCm39) |
missense |
probably benign |
0.06 |
R2511:Dnah12
|
UTSW |
14 |
26,491,907 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2875:Dnah12
|
UTSW |
14 |
26,598,907 (GRCm39) |
missense |
probably benign |
0.05 |
R2875:Dnah12
|
UTSW |
14 |
26,414,625 (GRCm39) |
missense |
probably benign |
0.04 |
R3551:Dnah12
|
UTSW |
14 |
26,492,929 (GRCm39) |
missense |
probably benign |
0.01 |
R3713:Dnah12
|
UTSW |
14 |
26,534,747 (GRCm39) |
missense |
probably benign |
|
R3729:Dnah12
|
UTSW |
14 |
26,427,220 (GRCm39) |
missense |
probably benign |
0.02 |
R3799:Dnah12
|
UTSW |
14 |
26,492,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R3846:Dnah12
|
UTSW |
14 |
26,431,366 (GRCm39) |
missense |
probably benign |
0.00 |
R3892:Dnah12
|
UTSW |
14 |
26,578,573 (GRCm39) |
missense |
probably benign |
0.03 |
R3921:Dnah12
|
UTSW |
14 |
26,493,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R3940:Dnah12
|
UTSW |
14 |
26,444,754 (GRCm39) |
missense |
probably benign |
|
R4065:Dnah12
|
UTSW |
14 |
26,492,405 (GRCm39) |
missense |
probably benign |
0.02 |
R4113:Dnah12
|
UTSW |
14 |
26,414,722 (GRCm39) |
missense |
probably damaging |
0.98 |
R4249:Dnah12
|
UTSW |
14 |
26,430,341 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4259:Dnah12
|
UTSW |
14 |
26,520,883 (GRCm39) |
missense |
probably benign |
0.01 |
R4260:Dnah12
|
UTSW |
14 |
26,520,883 (GRCm39) |
missense |
probably benign |
0.01 |
R4348:Dnah12
|
UTSW |
14 |
26,536,498 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4457:Dnah12
|
UTSW |
14 |
26,537,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R4490:Dnah12
|
UTSW |
14 |
26,455,758 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4491:Dnah12
|
UTSW |
14 |
26,455,758 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4494:Dnah12
|
UTSW |
14 |
26,593,812 (GRCm39) |
missense |
probably damaging |
0.99 |
R4523:Dnah12
|
UTSW |
14 |
26,598,915 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4523:Dnah12
|
UTSW |
14 |
26,491,979 (GRCm39) |
missense |
probably damaging |
0.97 |
R4546:Dnah12
|
UTSW |
14 |
26,494,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R4584:Dnah12
|
UTSW |
14 |
26,494,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R4624:Dnah12
|
UTSW |
14 |
26,456,913 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4689:Dnah12
|
UTSW |
14 |
26,427,994 (GRCm39) |
missense |
probably benign |
0.00 |
R4727:Dnah12
|
UTSW |
14 |
26,594,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Dnah12
|
UTSW |
14 |
26,503,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R4851:Dnah12
|
UTSW |
14 |
26,437,784 (GRCm39) |
nonsense |
probably null |
|
R4879:Dnah12
|
UTSW |
14 |
26,439,201 (GRCm39) |
critical splice donor site |
probably null |
|
R4893:Dnah12
|
UTSW |
14 |
26,431,325 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4915:Dnah12
|
UTSW |
14 |
26,455,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R4927:Dnah12
|
UTSW |
14 |
26,583,762 (GRCm39) |
nonsense |
probably null |
|
R4939:Dnah12
|
UTSW |
14 |
26,613,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R4962:Dnah12
|
UTSW |
14 |
26,437,855 (GRCm39) |
missense |
probably benign |
0.00 |
R5011:Dnah12
|
UTSW |
14 |
26,431,326 (GRCm39) |
missense |
probably benign |
0.03 |
R5013:Dnah12
|
UTSW |
14 |
26,431,326 (GRCm39) |
missense |
probably benign |
0.03 |
R5043:Dnah12
|
UTSW |
14 |
26,606,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R5049:Dnah12
|
UTSW |
14 |
26,456,852 (GRCm39) |
missense |
probably benign |
0.09 |
R5122:Dnah12
|
UTSW |
14 |
26,439,155 (GRCm39) |
missense |
probably benign |
0.00 |
R5135:Dnah12
|
UTSW |
14 |
26,492,434 (GRCm39) |
missense |
probably damaging |
0.99 |
R5149:Dnah12
|
UTSW |
14 |
26,572,883 (GRCm39) |
nonsense |
probably null |
|
R5154:Dnah12
|
UTSW |
14 |
26,571,320 (GRCm39) |
missense |
probably benign |
0.12 |
R5206:Dnah12
|
UTSW |
14 |
26,491,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R5307:Dnah12
|
UTSW |
14 |
26,414,641 (GRCm39) |
missense |
possibly damaging |
0.49 |
R5330:Dnah12
|
UTSW |
14 |
26,495,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R5335:Dnah12
|
UTSW |
14 |
26,601,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R5339:Dnah12
|
UTSW |
14 |
26,536,494 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5354:Dnah12
|
UTSW |
14 |
26,496,299 (GRCm39) |
splice site |
probably null |
|
R5389:Dnah12
|
UTSW |
14 |
26,456,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R5434:Dnah12
|
UTSW |
14 |
26,581,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R5466:Dnah12
|
UTSW |
14 |
26,493,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R5655:Dnah12
|
UTSW |
14 |
26,431,424 (GRCm39) |
missense |
probably benign |
0.01 |
R5681:Dnah12
|
UTSW |
14 |
26,537,452 (GRCm39) |
missense |
probably benign |
0.32 |
R5824:Dnah12
|
UTSW |
14 |
26,492,475 (GRCm39) |
critical splice donor site |
probably null |
|
R5863:Dnah12
|
UTSW |
14 |
26,576,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R5890:Dnah12
|
UTSW |
14 |
26,428,039 (GRCm39) |
missense |
probably benign |
0.09 |
R5912:Dnah12
|
UTSW |
14 |
26,491,965 (GRCm39) |
nonsense |
probably null |
|
R5916:Dnah12
|
UTSW |
14 |
26,428,073 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5941:Dnah12
|
UTSW |
14 |
26,428,022 (GRCm39) |
missense |
probably benign |
0.00 |
R5987:Dnah12
|
UTSW |
14 |
26,608,828 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5992:Dnah12
|
UTSW |
14 |
26,418,496 (GRCm39) |
missense |
probably benign |
0.04 |
R6132:Dnah12
|
UTSW |
14 |
26,439,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R6136:Dnah12
|
UTSW |
14 |
26,597,227 (GRCm39) |
missense |
probably damaging |
0.99 |
R6158:Dnah12
|
UTSW |
14 |
26,495,642 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6183:Dnah12
|
UTSW |
14 |
26,583,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R6191:Dnah12
|
UTSW |
14 |
26,431,412 (GRCm39) |
missense |
probably benign |
0.03 |
R6235:Dnah12
|
UTSW |
14 |
26,576,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Dnah12
|
UTSW |
14 |
26,492,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R6332:Dnah12
|
UTSW |
14 |
26,439,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R6334:Dnah12
|
UTSW |
14 |
26,427,989 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6443:Dnah12
|
UTSW |
14 |
26,600,008 (GRCm39) |
missense |
probably benign |
0.06 |
R6480:Dnah12
|
UTSW |
14 |
26,594,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R6530:Dnah12
|
UTSW |
14 |
26,456,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R6678:Dnah12
|
UTSW |
14 |
26,456,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R6709:Dnah12
|
UTSW |
14 |
26,594,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R6724:Dnah12
|
UTSW |
14 |
26,518,180 (GRCm39) |
missense |
probably benign |
0.02 |
R6745:Dnah12
|
UTSW |
14 |
26,428,383 (GRCm39) |
missense |
probably damaging |
0.99 |
R6788:Dnah12
|
UTSW |
14 |
26,523,470 (GRCm39) |
missense |
probably damaging |
0.99 |
R6894:Dnah12
|
UTSW |
14 |
26,456,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R6912:Dnah12
|
UTSW |
14 |
26,600,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R6982:Dnah12
|
UTSW |
14 |
26,521,033 (GRCm39) |
splice site |
probably null |
|
R7001:Dnah12
|
UTSW |
14 |
26,601,681 (GRCm39) |
missense |
probably damaging |
0.99 |
R7002:Dnah12
|
UTSW |
14 |
26,598,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R7017:Dnah12
|
UTSW |
14 |
26,456,835 (GRCm39) |
missense |
probably benign |
|
R7107:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7108:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7121:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7122:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7135:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7135:Dnah12
|
UTSW |
14 |
26,523,370 (GRCm39) |
missense |
probably damaging |
0.99 |
R7150:Dnah12
|
UTSW |
14 |
26,583,689 (GRCm39) |
missense |
probably damaging |
0.99 |
R7188:Dnah12
|
UTSW |
14 |
26,536,370 (GRCm39) |
missense |
probably benign |
0.04 |
R7201:Dnah12
|
UTSW |
14 |
26,536,579 (GRCm39) |
missense |
probably benign |
0.08 |
R7202:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7204:Dnah12
|
UTSW |
14 |
26,503,442 (GRCm39) |
missense |
probably damaging |
0.99 |
R7204:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7205:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7206:Dnah12
|
UTSW |
14 |
26,500,869 (GRCm39) |
critical splice donor site |
probably null |
|
R7219:Dnah12
|
UTSW |
14 |
26,576,837 (GRCm39) |
missense |
probably damaging |
0.99 |
R7337:Dnah12
|
UTSW |
14 |
26,488,534 (GRCm39) |
splice site |
probably null |
|
R7339:Dnah12
|
UTSW |
14 |
26,594,277 (GRCm39) |
missense |
probably benign |
|
R7363:Dnah12
|
UTSW |
14 |
26,445,766 (GRCm39) |
missense |
probably benign |
|
R7426:Dnah12
|
UTSW |
14 |
26,445,781 (GRCm39) |
missense |
probably benign |
0.01 |
R7472:Dnah12
|
UTSW |
14 |
26,578,592 (GRCm39) |
missense |
probably benign |
0.01 |
R7579:Dnah12
|
UTSW |
14 |
26,492,460 (GRCm39) |
missense |
probably benign |
0.05 |
R7655:Dnah12
|
UTSW |
14 |
26,581,273 (GRCm39) |
missense |
probably benign |
0.21 |
R7656:Dnah12
|
UTSW |
14 |
26,581,273 (GRCm39) |
missense |
probably benign |
0.21 |
R7694:Dnah12
|
UTSW |
14 |
26,503,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R7730:Dnah12
|
UTSW |
14 |
26,507,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R7837:Dnah12
|
UTSW |
14 |
26,518,176 (GRCm39) |
missense |
probably benign |
0.01 |
R7855:Dnah12
|
UTSW |
14 |
26,551,286 (GRCm39) |
missense |
probably benign |
0.14 |
R7870:Dnah12
|
UTSW |
14 |
26,578,486 (GRCm39) |
missense |
probably benign |
0.00 |
R7920:Dnah12
|
UTSW |
14 |
26,578,499 (GRCm39) |
missense |
possibly damaging |
0.58 |
R7933:Dnah12
|
UTSW |
14 |
26,488,072 (GRCm39) |
missense |
probably benign |
0.00 |
R7956:Dnah12
|
UTSW |
14 |
26,430,427 (GRCm39) |
missense |
probably damaging |
0.96 |
R8192:Dnah12
|
UTSW |
14 |
26,428,036 (GRCm39) |
missense |
probably benign |
|
R8263:Dnah12
|
UTSW |
14 |
26,613,421 (GRCm39) |
missense |
noncoding transcript |
|
R8287:Dnah12
|
UTSW |
14 |
26,534,560 (GRCm39) |
missense |
probably benign |
|
R8336:Dnah12
|
UTSW |
14 |
26,432,220 (GRCm39) |
missense |
probably benign |
0.01 |
R8362:Dnah12
|
UTSW |
14 |
26,576,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R8392:Dnah12
|
UTSW |
14 |
26,607,869 (GRCm39) |
missense |
probably benign |
|
R8458:Dnah12
|
UTSW |
14 |
26,548,849 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8481:Dnah12
|
UTSW |
14 |
26,575,753 (GRCm39) |
missense |
probably benign |
0.02 |
R8551:Dnah12
|
UTSW |
14 |
26,496,227 (GRCm39) |
missense |
probably damaging |
0.97 |
R8669:Dnah12
|
UTSW |
14 |
26,552,582 (GRCm39) |
splice site |
probably benign |
|
R8698:Dnah12
|
UTSW |
14 |
26,428,418 (GRCm39) |
missense |
probably benign |
0.02 |
R8709:Dnah12
|
UTSW |
14 |
26,414,757 (GRCm39) |
missense |
probably benign |
0.00 |
R8778:Dnah12
|
UTSW |
14 |
26,455,718 (GRCm39) |
missense |
probably benign |
0.29 |
R9049:Dnah12
|
UTSW |
14 |
26,443,275 (GRCm39) |
missense |
probably benign |
0.00 |
R9087:Dnah12
|
UTSW |
14 |
26,546,503 (GRCm39) |
missense |
probably damaging |
1.00 |
R9099:Dnah12
|
UTSW |
14 |
26,492,325 (GRCm39) |
missense |
probably benign |
0.31 |
R9153:Dnah12
|
UTSW |
14 |
26,536,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R9177:Dnah12
|
UTSW |
14 |
26,571,255 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9214:Dnah12
|
UTSW |
14 |
26,445,060 (GRCm39) |
missense |
probably benign |
0.02 |
R9268:Dnah12
|
UTSW |
14 |
26,571,255 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9274:Dnah12
|
UTSW |
14 |
26,537,374 (GRCm39) |
missense |
probably benign |
0.00 |
R9293:Dnah12
|
UTSW |
14 |
26,495,016 (GRCm39) |
missense |
probably benign |
|
R9322:Dnah12
|
UTSW |
14 |
26,492,934 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9353:Dnah12
|
UTSW |
14 |
26,578,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R9506:Dnah12
|
UTSW |
14 |
26,514,168 (GRCm39) |
missense |
probably benign |
0.00 |
R9518:Dnah12
|
UTSW |
14 |
26,495,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R9524:Dnah12
|
UTSW |
14 |
26,572,494 (GRCm39) |
missense |
probably null |
0.91 |
R9562:Dnah12
|
UTSW |
14 |
26,597,281 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9565:Dnah12
|
UTSW |
14 |
26,597,281 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9573:Dnah12
|
UTSW |
14 |
26,414,619 (GRCm39) |
missense |
probably benign |
|
R9581:Dnah12
|
UTSW |
14 |
26,491,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R9689:Dnah12
|
UTSW |
14 |
26,590,871 (GRCm39) |
missense |
probably null |
1.00 |
R9727:Dnah12
|
UTSW |
14 |
26,523,510 (GRCm39) |
nonsense |
probably null |
|
V7580:Dnah12
|
UTSW |
14 |
26,495,050 (GRCm39) |
missense |
possibly damaging |
0.95 |
V7581:Dnah12
|
UTSW |
14 |
26,495,050 (GRCm39) |
missense |
possibly damaging |
0.95 |
X0018:Dnah12
|
UTSW |
14 |
26,536,437 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Dnah12
|
UTSW |
14 |
26,538,245 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Dnah12
|
UTSW |
14 |
26,536,602 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1177:Dnah12
|
UTSW |
14 |
26,597,172 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- CCCAGTGTCTCATGAGGTAATCTAC -3'
(R):5'- TGGAGCAGCTTGACTATAACATAC -3'
Sequencing Primer
(F):5'- GACTGATGGTATTGTGGCAA -3'
(R):5'- GACTATAGCATAACCTTTACGA -3'
|
Posted On |
2015-11-11 |