Incidental Mutation 'R7203:Spata31h1'
| ID |
560805 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Spata31h1
|
| Ensembl Gene |
ENSMUSG00000044581 |
| Gene Name |
SPATA31 subfamily H member 1 |
| Synonyms |
4932415D10Rik |
| MMRRC Submission |
045281-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.063)
|
| Stock # |
R7203 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
10 |
| Chromosomal Location |
82117950-82152416 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to A
at 82129248 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 1254
(T1254I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151425
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000217661]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217661
AA Change: T1254I
PolyPhen 2
Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
100% (108/108) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 108 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930544G11Rik |
T |
C |
6: 65,930,317 (GRCm39) |
V184A |
probably benign |
Het |
| Aars2 |
A |
G |
17: 45,827,497 (GRCm39) |
Y513C |
probably damaging |
Het |
| Ackr2 |
G |
A |
9: 121,738,033 (GRCm39) |
C136Y |
probably damaging |
Het |
| Aldh1l1 |
A |
G |
6: 90,547,782 (GRCm39) |
K414R |
probably benign |
Het |
| Arl9 |
A |
G |
5: 77,155,118 (GRCm39) |
Y83C |
possibly damaging |
Het |
| Atp10a |
G |
T |
7: 58,436,221 (GRCm39) |
R337L |
probably benign |
Het |
| Atp6v1g3 |
A |
T |
1: 138,215,538 (GRCm39) |
Q66L |
probably damaging |
Het |
| Atp7b |
A |
T |
8: 22,487,351 (GRCm39) |
N1321K |
probably damaging |
Het |
| Axdnd1 |
A |
T |
1: 156,209,959 (GRCm39) |
M437K |
probably damaging |
Het |
| Bap1 |
C |
A |
14: 30,976,126 (GRCm39) |
P147Q |
probably damaging |
Het |
| Bicd1 |
C |
T |
6: 149,414,403 (GRCm39) |
T372I |
possibly damaging |
Het |
| Brix1 |
T |
C |
15: 10,483,378 (GRCm39) |
|
probably null |
Het |
| Btrc |
A |
G |
19: 45,501,967 (GRCm39) |
|
probably null |
Het |
| C130050O18Rik |
A |
C |
5: 139,400,129 (GRCm39) |
I61L |
probably benign |
Het |
| Cfap161 |
A |
G |
7: 83,425,258 (GRCm39) |
S278P |
probably damaging |
Het |
| Cgnl1 |
T |
C |
9: 71,631,815 (GRCm39) |
D512G |
possibly damaging |
Het |
| Chat |
T |
C |
14: 32,141,014 (GRCm39) |
D461G |
probably damaging |
Het |
| Chl1 |
T |
A |
6: 103,668,635 (GRCm39) |
V456D |
probably benign |
Het |
| Cib1 |
T |
C |
7: 79,882,120 (GRCm39) |
T20A |
possibly damaging |
Het |
| Cubn |
T |
G |
2: 13,355,814 (GRCm39) |
H1806P |
probably benign |
Het |
| Dapk1 |
T |
A |
13: 60,844,149 (GRCm39) |
V56E |
possibly damaging |
Het |
| Dennd4a |
A |
G |
9: 64,803,756 (GRCm39) |
N1032D |
probably benign |
Het |
| Dlg5 |
T |
A |
14: 24,188,723 (GRCm39) |
E1756V |
probably damaging |
Het |
| Dnah1 |
T |
C |
14: 30,996,339 (GRCm39) |
T2666A |
probably benign |
Het |
| Dnah11 |
A |
T |
12: 118,009,257 (GRCm39) |
I2135N |
possibly damaging |
Het |
| Dnah6 |
T |
A |
6: 73,150,528 (GRCm39) |
E745V |
probably benign |
Het |
| Dock8 |
A |
T |
19: 25,158,927 (GRCm39) |
N1695I |
probably damaging |
Het |
| Esf1 |
C |
T |
2: 140,006,139 (GRCm39) |
R336Q |
possibly damaging |
Het |
| Fam161a |
A |
G |
11: 22,971,664 (GRCm39) |
|
probably null |
Het |
| Fam89a |
T |
C |
8: 125,478,418 (GRCm39) |
E44G |
possibly damaging |
Het |
| Fndc3b |
A |
T |
3: 27,510,634 (GRCm39) |
D829E |
probably benign |
Het |
| Fxr1 |
C |
T |
3: 34,100,689 (GRCm39) |
T125I |
possibly damaging |
Het |
| Gfer |
T |
C |
17: 24,914,836 (GRCm39) |
D69G |
probably damaging |
Het |
| Gpatch2l |
T |
A |
12: 86,335,711 (GRCm39) |
S471T |
probably benign |
Het |
| Grm7 |
T |
G |
6: 111,335,530 (GRCm39) |
I647S |
possibly damaging |
Het |
| Gsn |
A |
G |
2: 35,188,807 (GRCm39) |
I447V |
probably benign |
Het |
| H2al2c |
C |
T |
Y: 2,599,234 (GRCm39) |
L46F |
possibly damaging |
Het |
| Hao2 |
A |
C |
3: 98,784,598 (GRCm39) |
|
probably null |
Het |
| Ifitm10 |
T |
C |
7: 141,882,305 (GRCm39) |
E155G |
probably benign |
Het |
| Igkv8-16 |
C |
A |
6: 70,363,794 (GRCm39) |
W76L |
probably benign |
Het |
| Igsf21 |
A |
T |
4: 139,834,648 (GRCm39) |
F75I |
possibly damaging |
Het |
| Ints14 |
T |
A |
9: 64,871,701 (GRCm39) |
M13K |
probably damaging |
Het |
| Ipmk |
A |
T |
10: 71,199,298 (GRCm39) |
D53V |
possibly damaging |
Het |
| Iqcn |
A |
T |
8: 71,169,597 (GRCm39) |
E1229V |
probably benign |
Het |
| Itga8 |
A |
G |
2: 12,234,906 (GRCm39) |
F451L |
possibly damaging |
Het |
| Jup |
A |
G |
11: 100,272,560 (GRCm39) |
F284S |
probably damaging |
Het |
| Kctd5 |
T |
C |
17: 24,292,209 (GRCm39) |
D65G |
probably benign |
Het |
| Klrc1 |
A |
T |
6: 129,654,184 (GRCm39) |
S148T |
probably benign |
Het |
| Kmt5b |
A |
G |
19: 3,864,147 (GRCm39) |
K404E |
probably damaging |
Het |
| Krt9 |
A |
C |
11: 100,081,617 (GRCm39) |
M304R |
probably damaging |
Het |
| Krtap5-1 |
A |
T |
7: 141,850,299 (GRCm39) |
S143T |
unknown |
Het |
| Kyat3 |
A |
G |
3: 142,426,162 (GRCm39) |
N68D |
probably damaging |
Het |
| Kynu |
A |
G |
2: 43,571,365 (GRCm39) |
D427G |
probably damaging |
Het |
| Leo1 |
A |
G |
9: 75,353,278 (GRCm39) |
|
probably null |
Het |
| Loxhd1 |
A |
G |
18: 77,501,892 (GRCm39) |
D1737G |
probably damaging |
Het |
| Lpo |
C |
A |
11: 87,700,077 (GRCm39) |
L521F |
possibly damaging |
Het |
| Lrrk1 |
A |
G |
7: 65,920,573 (GRCm39) |
S1477P |
probably damaging |
Het |
| Lrrtm1 |
C |
A |
6: 77,220,584 (GRCm39) |
L14M |
probably damaging |
Het |
| Ly75 |
G |
A |
2: 60,154,196 (GRCm39) |
R1084* |
probably null |
Het |
| Mcf2l |
A |
G |
8: 13,060,456 (GRCm39) |
D764G |
probably benign |
Het |
| Mmut |
A |
T |
17: 41,249,564 (GRCm39) |
M180L |
probably benign |
Het |
| Mrgprd |
A |
T |
7: 144,876,086 (GRCm39) |
D319V |
probably benign |
Het |
| Myom3 |
T |
C |
4: 135,522,490 (GRCm39) |
L897P |
possibly damaging |
Het |
| Ncapd2 |
A |
T |
6: 125,161,291 (GRCm39) |
M247K |
possibly damaging |
Het |
| Nlrp2 |
T |
C |
7: 5,320,533 (GRCm39) |
D868G |
probably damaging |
Het |
| Npy6r |
A |
G |
18: 44,408,999 (GRCm39) |
N140S |
probably damaging |
Het |
| Nsmce4a |
T |
C |
7: 130,141,602 (GRCm39) |
K196E |
probably benign |
Het |
| Nup88 |
T |
C |
11: 70,836,080 (GRCm39) |
K532R |
probably benign |
Het |
| Or6k4 |
T |
A |
1: 173,964,680 (GRCm39) |
Y123* |
probably null |
Het |
| Or8d6 |
T |
A |
9: 39,853,805 (GRCm39) |
V83E |
probably benign |
Het |
| Or8g29-ps1 |
A |
T |
9: 39,200,589 (GRCm39) |
I199N |
unknown |
Het |
| Pbxip1 |
A |
T |
3: 89,354,735 (GRCm39) |
D418V |
possibly damaging |
Het |
| Pde2a |
C |
A |
7: 101,159,151 (GRCm39) |
R761S |
possibly damaging |
Het |
| Phf10 |
A |
T |
17: 15,166,575 (GRCm39) |
C432S |
probably damaging |
Het |
| Pitpnm2 |
T |
C |
5: 124,259,522 (GRCm39) |
D1271G |
probably damaging |
Het |
| Plin1 |
A |
T |
7: 79,373,192 (GRCm39) |
L259Q |
probably damaging |
Het |
| Pmpca |
G |
C |
2: 26,285,046 (GRCm39) |
E424Q |
possibly damaging |
Het |
| Pou6f2 |
T |
A |
13: 18,414,379 (GRCm39) |
Q132L |
unknown |
Het |
| Ppa2 |
A |
T |
3: 133,036,199 (GRCm39) |
N118Y |
possibly damaging |
Het |
| Prickle2 |
T |
C |
6: 92,387,959 (GRCm39) |
E537G |
possibly damaging |
Het |
| Prl3d1 |
A |
G |
13: 27,282,684 (GRCm39) |
I141V |
possibly damaging |
Het |
| Prl8a1 |
A |
T |
13: 27,758,172 (GRCm39) |
V179D |
probably damaging |
Het |
| Prr14l |
A |
G |
5: 32,984,489 (GRCm39) |
F1669L |
probably benign |
Het |
| Prrg4 |
T |
A |
2: 104,669,787 (GRCm39) |
E110V |
possibly damaging |
Het |
| Rfx5 |
C |
A |
3: 94,866,187 (GRCm39) |
H495Q |
unknown |
Het |
| Rgl2 |
C |
T |
17: 34,152,403 (GRCm39) |
R367W |
probably damaging |
Het |
| Rpe65 |
A |
G |
3: 159,328,491 (GRCm39) |
Y433C |
probably damaging |
Het |
| Rpl35rt |
A |
T |
1: 156,193,657 (GRCm39) |
I4F |
probably damaging |
Het |
| Rtn4rl1 |
C |
T |
11: 75,156,576 (GRCm39) |
S336F |
possibly damaging |
Het |
| Scn2a |
A |
G |
2: 65,578,663 (GRCm39) |
D1446G |
probably benign |
Het |
| Sdk1 |
C |
A |
5: 142,031,931 (GRCm39) |
T1002K |
probably benign |
Het |
| Slc9b2 |
T |
C |
3: 135,036,422 (GRCm39) |
S409P |
probably benign |
Het |
| Sowahc |
A |
G |
10: 59,058,100 (GRCm39) |
T79A |
probably benign |
Het |
| Stk35 |
T |
A |
2: 129,643,513 (GRCm39) |
C166S |
probably benign |
Het |
| Tarbp2 |
A |
G |
15: 102,430,922 (GRCm39) |
H225R |
probably benign |
Het |
| Tdrd12 |
T |
A |
7: 35,188,648 (GRCm39) |
K530* |
probably null |
Het |
| Terf2ip |
A |
G |
8: 112,744,618 (GRCm39) |
I312V |
probably benign |
Het |
| Tgfb1 |
T |
C |
7: 25,391,964 (GRCm39) |
|
probably null |
Het |
| Thbs2 |
T |
C |
17: 14,891,720 (GRCm39) |
D939G |
probably damaging |
Het |
| Ube4b |
A |
T |
4: 149,483,067 (GRCm39) |
I67K |
probably benign |
Het |
| Ubn1 |
G |
T |
16: 4,895,080 (GRCm39) |
V709F |
possibly damaging |
Het |
| Ugt2b5 |
T |
C |
5: 87,276,258 (GRCm39) |
K339E |
possibly damaging |
Het |
| Vax2 |
T |
C |
6: 83,714,882 (GRCm39) |
S266P |
probably damaging |
Het |
| Vmn2r108 |
A |
G |
17: 20,683,038 (GRCm39) |
I722T |
probably benign |
Het |
| Vmn2r95 |
A |
G |
17: 18,661,577 (GRCm39) |
K441R |
probably benign |
Het |
| Wapl |
C |
A |
14: 34,458,648 (GRCm39) |
D903E |
probably benign |
Het |
| Wee1 |
T |
A |
7: 109,734,001 (GRCm39) |
V442D |
probably benign |
Het |
| Zan |
T |
C |
5: 137,432,358 (GRCm39) |
N2313S |
unknown |
Het |
|
| Other mutations in Spata31h1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00090:Spata31h1
|
APN |
10 |
82,119,586 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL01457:Spata31h1
|
APN |
10 |
82,120,568 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01540:Spata31h1
|
APN |
10 |
82,120,016 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
IGL02693:Spata31h1
|
APN |
10 |
82,121,092 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL02867:Spata31h1
|
APN |
10 |
82,119,654 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL02889:Spata31h1
|
APN |
10 |
82,119,654 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL03080:Spata31h1
|
APN |
10 |
82,119,816 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03120:Spata31h1
|
APN |
10 |
82,120,869 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
IGL03351:Spata31h1
|
APN |
10 |
82,119,401 (GRCm39) |
utr 3 prime |
probably benign |
|
|
FR4449:Spata31h1
|
UTSW |
10 |
82,121,303 (GRCm39) |
frame shift |
probably null |
|
|
FR4548:Spata31h1
|
UTSW |
10 |
82,126,830 (GRCm39) |
small insertion |
probably benign |
|
|
FR4737:Spata31h1
|
UTSW |
10 |
82,121,303 (GRCm39) |
small deletion |
probably benign |
|
|
PIT4480001:Spata31h1
|
UTSW |
10 |
82,119,586 (GRCm39) |
missense |
probably benign |
0.06 |
|
R0102:Spata31h1
|
UTSW |
10 |
82,119,390 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0312:Spata31h1
|
UTSW |
10 |
82,120,203 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1303:Spata31h1
|
UTSW |
10 |
82,120,390 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R2039:Spata31h1
|
UTSW |
10 |
82,120,510 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2356:Spata31h1
|
UTSW |
10 |
82,119,789 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4740:Spata31h1
|
UTSW |
10 |
82,119,481 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R4857:Spata31h1
|
UTSW |
10 |
82,119,682 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R5017:Spata31h1
|
UTSW |
10 |
82,132,510 (GRCm39) |
missense |
unknown |
|
|
R5095:Spata31h1
|
UTSW |
10 |
82,119,501 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5209:Spata31h1
|
UTSW |
10 |
82,119,652 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R5388:Spata31h1
|
UTSW |
10 |
82,119,561 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5642:Spata31h1
|
UTSW |
10 |
82,120,317 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5646:Spata31h1
|
UTSW |
10 |
82,119,610 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6188:Spata31h1
|
UTSW |
10 |
82,121,091 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R6215:Spata31h1
|
UTSW |
10 |
82,126,946 (GRCm39) |
missense |
probably benign |
0.07 |
|
R6252:Spata31h1
|
UTSW |
10 |
82,119,588 (GRCm39) |
missense |
probably benign |
0.30 |
|
R6275:Spata31h1
|
UTSW |
10 |
82,121,202 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6303:Spata31h1
|
UTSW |
10 |
82,126,202 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6304:Spata31h1
|
UTSW |
10 |
82,126,202 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R6313:Spata31h1
|
UTSW |
10 |
82,129,470 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6323:Spata31h1
|
UTSW |
10 |
82,118,916 (GRCm39) |
missense |
probably benign |
0.27 |
|
R6374:Spata31h1
|
UTSW |
10 |
82,124,731 (GRCm39) |
unclassified |
probably benign |
|
|
R6407:Spata31h1
|
UTSW |
10 |
82,129,645 (GRCm39) |
missense |
probably benign |
0.16 |
|
R6468:Spata31h1
|
UTSW |
10 |
82,131,150 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6490:Spata31h1
|
UTSW |
10 |
82,125,138 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R6605:Spata31h1
|
UTSW |
10 |
82,131,871 (GRCm39) |
missense |
probably benign |
0.27 |
|
R6614:Spata31h1
|
UTSW |
10 |
82,127,482 (GRCm39) |
missense |
probably benign |
0.31 |
|
R6626:Spata31h1
|
UTSW |
10 |
82,128,667 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6630:Spata31h1
|
UTSW |
10 |
82,122,906 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R6646:Spata31h1
|
UTSW |
10 |
82,132,664 (GRCm39) |
missense |
unknown |
|
|
R6723:Spata31h1
|
UTSW |
10 |
82,125,657 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
R6751:Spata31h1
|
UTSW |
10 |
82,119,331 (GRCm39) |
missense |
probably benign |
0.06 |
|
R6850:Spata31h1
|
UTSW |
10 |
82,128,888 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R6944:Spata31h1
|
UTSW |
10 |
82,132,056 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6957:Spata31h1
|
UTSW |
10 |
82,129,620 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6988:Spata31h1
|
UTSW |
10 |
82,127,733 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R7069:Spata31h1
|
UTSW |
10 |
82,125,777 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7164:Spata31h1
|
UTSW |
10 |
82,122,063 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7175:Spata31h1
|
UTSW |
10 |
82,122,583 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7201:Spata31h1
|
UTSW |
10 |
82,127,461 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7205:Spata31h1
|
UTSW |
10 |
82,125,161 (GRCm39) |
missense |
probably benign |
0.35 |
|
R7241:Spata31h1
|
UTSW |
10 |
82,122,876 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7283:Spata31h1
|
UTSW |
10 |
82,127,131 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7305:Spata31h1
|
UTSW |
10 |
82,120,953 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7358:Spata31h1
|
UTSW |
10 |
82,127,847 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R7360:Spata31h1
|
UTSW |
10 |
82,132,341 (GRCm39) |
missense |
unknown |
|
|
R7362:Spata31h1
|
UTSW |
10 |
82,128,831 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R7385:Spata31h1
|
UTSW |
10 |
82,123,729 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7385:Spata31h1
|
UTSW |
10 |
82,123,571 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7472:Spata31h1
|
UTSW |
10 |
82,119,421 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7493:Spata31h1
|
UTSW |
10 |
82,152,264 (GRCm39) |
missense |
unknown |
|
|
R7493:Spata31h1
|
UTSW |
10 |
82,124,798 (GRCm39) |
nonsense |
probably null |
|
|
R7498:Spata31h1
|
UTSW |
10 |
82,127,113 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7512:Spata31h1
|
UTSW |
10 |
82,128,469 (GRCm39) |
missense |
probably benign |
0.31 |
|
R7560:Spata31h1
|
UTSW |
10 |
82,120,449 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7591:Spata31h1
|
UTSW |
10 |
82,128,046 (GRCm39) |
missense |
probably benign |
0.16 |
|
R7636:Spata31h1
|
UTSW |
10 |
82,130,973 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7640:Spata31h1
|
UTSW |
10 |
82,130,490 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7709:Spata31h1
|
UTSW |
10 |
82,126,366 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R7790:Spata31h1
|
UTSW |
10 |
82,123,329 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7875:Spata31h1
|
UTSW |
10 |
82,123,456 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R7878:Spata31h1
|
UTSW |
10 |
82,119,856 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7899:Spata31h1
|
UTSW |
10 |
82,118,731 (GRCm39) |
missense |
unknown |
|
|
R7905:Spata31h1
|
UTSW |
10 |
82,131,936 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7975:Spata31h1
|
UTSW |
10 |
82,119,823 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7988:Spata31h1
|
UTSW |
10 |
82,131,934 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8076:Spata31h1
|
UTSW |
10 |
82,132,520 (GRCm39) |
nonsense |
probably null |
|
|
R8144:Spata31h1
|
UTSW |
10 |
82,130,433 (GRCm39) |
nonsense |
probably null |
|
|
R8429:Spata31h1
|
UTSW |
10 |
82,125,301 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R8465:Spata31h1
|
UTSW |
10 |
82,152,298 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R8470:Spata31h1
|
UTSW |
10 |
82,126,314 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8509:Spata31h1
|
UTSW |
10 |
82,126,950 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8515:Spata31h1
|
UTSW |
10 |
82,124,436 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8672:Spata31h1
|
UTSW |
10 |
82,127,726 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8700:Spata31h1
|
UTSW |
10 |
82,127,859 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R8827:Spata31h1
|
UTSW |
10 |
82,129,617 (GRCm39) |
missense |
probably benign |
0.07 |
|
R8872:Spata31h1
|
UTSW |
10 |
82,128,619 (GRCm39) |
missense |
probably benign |
0.07 |
|
R8875:Spata31h1
|
UTSW |
10 |
82,123,476 (GRCm39) |
missense |
probably benign |
0.16 |
|
R8884:Spata31h1
|
UTSW |
10 |
82,119,486 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R8906:Spata31h1
|
UTSW |
10 |
82,122,379 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8924:Spata31h1
|
UTSW |
10 |
82,131,295 (GRCm39) |
missense |
probably benign |
0.03 |
|
R8949:Spata31h1
|
UTSW |
10 |
82,123,753 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8957:Spata31h1
|
UTSW |
10 |
82,124,908 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9042:Spata31h1
|
UTSW |
10 |
82,123,185 (GRCm39) |
missense |
probably benign |
0.08 |
|
R9056:Spata31h1
|
UTSW |
10 |
82,127,101 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9062:Spata31h1
|
UTSW |
10 |
82,126,945 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9074:Spata31h1
|
UTSW |
10 |
82,123,894 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R9086:Spata31h1
|
UTSW |
10 |
82,124,577 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9113:Spata31h1
|
UTSW |
10 |
82,131,352 (GRCm39) |
nonsense |
probably null |
|
|
R9119:Spata31h1
|
UTSW |
10 |
82,131,553 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9132:Spata31h1
|
UTSW |
10 |
82,127,896 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R9141:Spata31h1
|
UTSW |
10 |
82,126,610 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9151:Spata31h1
|
UTSW |
10 |
82,120,928 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9155:Spata31h1
|
UTSW |
10 |
82,120,203 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9159:Spata31h1
|
UTSW |
10 |
82,118,524 (GRCm39) |
nonsense |
probably null |
|
|
R9197:Spata31h1
|
UTSW |
10 |
82,120,401 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9212:Spata31h1
|
UTSW |
10 |
82,118,979 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9245:Spata31h1
|
UTSW |
10 |
82,123,554 (GRCm39) |
missense |
probably benign |
0.10 |
|
R9304:Spata31h1
|
UTSW |
10 |
82,131,930 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9309:Spata31h1
|
UTSW |
10 |
82,130,986 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9329:Spata31h1
|
UTSW |
10 |
82,121,439 (GRCm39) |
missense |
probably benign |
0.06 |
|
R9356:Spata31h1
|
UTSW |
10 |
82,125,157 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R9423:Spata31h1
|
UTSW |
10 |
82,123,459 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R9426:Spata31h1
|
UTSW |
10 |
82,126,610 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9457:Spata31h1
|
UTSW |
10 |
82,122,573 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9509:Spata31h1
|
UTSW |
10 |
82,132,229 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9612:Spata31h1
|
UTSW |
10 |
82,125,453 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R9674:Spata31h1
|
UTSW |
10 |
82,120,030 (GRCm39) |
missense |
possibly damaging |
0.69 |
|
R9726:Spata31h1
|
UTSW |
10 |
82,118,605 (GRCm39) |
missense |
unknown |
|
|
RF017:Spata31h1
|
UTSW |
10 |
82,126,826 (GRCm39) |
small insertion |
probably benign |
|
|
RF055:Spata31h1
|
UTSW |
10 |
82,126,827 (GRCm39) |
small insertion |
probably benign |
|
|
Z1176:Spata31h1
|
UTSW |
10 |
82,129,062 (GRCm39) |
missense |
probably benign |
0.03 |
|
Z1176:Spata31h1
|
UTSW |
10 |
82,125,730 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
Z1176:Spata31h1
|
UTSW |
10 |
82,118,371 (GRCm39) |
missense |
unknown |
|
|
Z1177:Spata31h1
|
UTSW |
10 |
82,123,251 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Z1177:Spata31h1
|
UTSW |
10 |
82,122,960 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
Z1177:Spata31h1
|
UTSW |
10 |
82,121,632 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
Z1177:Spata31h1
|
UTSW |
10 |
82,125,520 (GRCm39) |
nonsense |
probably null |
|
|
Z1187:Spata31h1
|
UTSW |
10 |
82,124,390 (GRCm39) |
small deletion |
probably benign |
|
|
| Predicted Primers |
PCR Primer
(F):5'- GGTATCTTGTTCCCAAGGTCC -3'
(R):5'- TACCATGTTCCCCAATGCCAG -3'
Sequencing Primer
(F):5'- GATATCCCGCATGAACGCTGTAG -3'
(R):5'- TGCCAGAAATCAGATCATCTGG -3'
|
| Posted On |
2019-06-26 |
Incidental Mutation