Incidental Mutation 'R7205:Spata31h1'
| ID |
560543 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Spata31h1
|
| Ensembl Gene |
ENSMUSG00000044581 |
| Gene Name |
SPATA31 subfamily H member 1 |
| Synonyms |
4932415D10Rik |
| MMRRC Submission |
045283-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.072)
|
| Stock # |
R7205 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
10 |
| Chromosomal Location |
82117950-82152416 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 82125161 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glutamic Acid
at position 2616
(D2616E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151425
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000171401]
[ENSMUST00000217661]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000171401
|
| SMART Domains |
Protein: ENSMUSP00000126178
Gene: ENSMUSG00000044581
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
5 |
16 |
N/A |
INTRINSIC |
|
low complexity region
|
241 |
263 |
N/A |
INTRINSIC |
|
low complexity region
|
387 |
405 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000217661
AA Change: D2616E
PolyPhen 2
Score 0.346 (Sensitivity: 0.90; Specificity: 0.89)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
97% (99/102) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 101 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca15 |
A |
T |
7: 119,993,587 (GRCm39) |
K1269M |
possibly damaging |
Het |
| Adgrl2 |
A |
T |
3: 148,564,585 (GRCm39) |
Y332N |
probably damaging |
Het |
| Adgrv1 |
C |
T |
13: 81,627,777 (GRCm39) |
V3695I |
probably benign |
Het |
| Aldh1l1 |
A |
T |
6: 90,575,257 (GRCm39) |
Y848F |
probably damaging |
Het |
| Ambra1 |
T |
C |
2: 91,598,103 (GRCm39) |
V88A |
possibly damaging |
Het |
| Ankrd12 |
C |
T |
17: 66,292,160 (GRCm39) |
R1091Q |
probably damaging |
Het |
| Apob |
T |
G |
12: 8,055,087 (GRCm39) |
V1362G |
probably damaging |
Het |
| Arhgap17 |
A |
G |
7: 122,905,661 (GRCm39) |
L328P |
probably damaging |
Het |
| Arhgap27 |
A |
C |
11: 103,235,367 (GRCm39) |
V9G |
probably benign |
Het |
| Arhgap33 |
A |
T |
7: 30,232,434 (GRCm39) |
D34E |
probably damaging |
Het |
| Ash1l |
A |
G |
3: 88,873,259 (GRCm39) |
D14G |
probably benign |
Het |
| Atf6b |
T |
C |
17: 34,872,703 (GRCm39) |
Y575H |
probably damaging |
Het |
| Bcl2l2 |
T |
G |
14: 55,122,058 (GRCm39) |
S74A |
probably benign |
Het |
| Begain |
T |
C |
12: 109,004,794 (GRCm39) |
T73A |
possibly damaging |
Het |
| Bicdl1 |
C |
T |
5: 115,808,340 (GRCm39) |
R264Q |
probably damaging |
Het |
| Ccdc180 |
A |
G |
4: 45,914,588 (GRCm39) |
D701G |
probably benign |
Het |
| Cd200r4 |
G |
T |
16: 44,653,529 (GRCm39) |
V146L |
probably damaging |
Het |
| Cd226 |
G |
A |
18: 89,265,322 (GRCm39) |
C200Y |
probably damaging |
Het |
| Cdcp3 |
T |
C |
7: 130,879,352 (GRCm39) |
|
probably null |
Het |
| Cdhr18 |
T |
C |
14: 13,866,032 (GRCm38) |
T286A |
|
Het |
| Cdk12 |
A |
G |
11: 98,115,451 (GRCm39) |
N864S |
unknown |
Het |
| Cfhr4 |
A |
T |
1: 139,680,788 (GRCm39) |
Y243* |
probably null |
Het |
| Clcnkb |
A |
T |
4: 141,135,946 (GRCm39) |
L413Q |
probably damaging |
Het |
| Cldn10 |
T |
C |
14: 119,099,255 (GRCm39) |
V123A |
possibly damaging |
Het |
| Cnn1 |
T |
A |
9: 22,017,078 (GRCm39) |
|
probably null |
Het |
| Cpa5 |
C |
A |
6: 30,630,829 (GRCm39) |
Q364K |
probably benign |
Het |
| Cstdc5 |
T |
C |
16: 36,187,809 (GRCm39) |
I19V |
probably benign |
Het |
| Ddx11 |
A |
G |
17: 66,437,766 (GRCm39) |
E164G |
probably benign |
Het |
| Dnah12 |
G |
A |
14: 26,500,869 (GRCm39) |
|
probably null |
Het |
| Drc7 |
T |
A |
8: 95,804,549 (GRCm39) |
Y855N |
probably damaging |
Het |
| Fam20b |
C |
A |
1: 156,529,968 (GRCm39) |
|
probably null |
Het |
| Fip1l1 |
T |
A |
5: 74,748,736 (GRCm39) |
|
probably null |
Het |
| Flt4 |
A |
G |
11: 49,525,125 (GRCm39) |
D657G |
probably null |
Het |
| Fmo3 |
T |
A |
1: 162,781,857 (GRCm39) |
T499S |
possibly damaging |
Het |
| Fyco1 |
C |
T |
9: 123,651,491 (GRCm39) |
G1190S |
probably benign |
Het |
| Galnt17 |
C |
A |
5: 131,335,590 (GRCm39) |
|
probably benign |
Het |
| Ggcx |
T |
C |
6: 72,404,987 (GRCm39) |
I465T |
probably damaging |
Het |
| Gm7361 |
T |
A |
5: 26,466,116 (GRCm39) |
N159K |
probably damaging |
Het |
| Golgb1 |
A |
G |
16: 36,695,663 (GRCm39) |
N54S |
unknown |
Het |
| Grin2c |
G |
A |
11: 115,141,876 (GRCm39) |
P848S |
probably damaging |
Het |
| Grina |
T |
C |
15: 76,133,287 (GRCm39) |
V285A |
probably damaging |
Het |
| Gtpbp6 |
A |
G |
5: 110,252,478 (GRCm39) |
L381P |
probably damaging |
Het |
| Herc2 |
G |
T |
7: 55,832,388 (GRCm39) |
G3028V |
probably damaging |
Het |
| Ibsp |
A |
T |
5: 104,458,297 (GRCm39) |
Y278F |
probably damaging |
Het |
| Ints4 |
T |
A |
7: 97,184,433 (GRCm39) |
L846* |
probably null |
Het |
| Kif17 |
A |
G |
4: 138,021,077 (GRCm39) |
K849E |
probably benign |
Het |
| Krt77 |
G |
A |
15: 101,777,806 (GRCm39) |
P83L |
probably benign |
Het |
| Ky |
T |
G |
9: 102,419,491 (GRCm39) |
D499E |
probably damaging |
Het |
| Lrp3 |
A |
T |
7: 34,902,051 (GRCm39) |
M610K |
probably damaging |
Het |
| Lrrfip1 |
T |
A |
1: 91,019,338 (GRCm39) |
D156E |
probably benign |
Het |
| Map6 |
C |
A |
7: 98,918,257 (GRCm39) |
H343Q |
probably benign |
Het |
| Micu2 |
G |
T |
14: 58,191,606 (GRCm39) |
D148E |
probably benign |
Het |
| Mks1 |
T |
A |
11: 87,747,428 (GRCm39) |
S153T |
probably benign |
Het |
| Msantd5f3 |
A |
G |
4: 73,573,157 (GRCm39) |
Y132C |
probably damaging |
Het |
| Muc6 |
AGGCGCAGAAACCCTGGC |
AGGC |
7: 141,214,363 (GRCm39) |
|
probably null |
Het |
| Myh9 |
T |
C |
15: 77,667,672 (GRCm39) |
K587R |
probably benign |
Het |
| Neb |
T |
C |
2: 52,086,368 (GRCm39) |
Y5478C |
probably damaging |
Het |
| Nelfe |
G |
A |
17: 35,069,912 (GRCm39) |
|
probably null |
Het |
| Nps |
T |
A |
7: 134,870,510 (GRCm39) |
L11I |
probably damaging |
Het |
| Nsd1 |
A |
T |
13: 55,394,283 (GRCm39) |
D731V |
probably damaging |
Het |
| Nup50 |
A |
G |
15: 84,817,859 (GRCm39) |
T93A |
probably benign |
Het |
| Nup98 |
A |
T |
7: 101,844,248 (GRCm39) |
F29Y |
unknown |
Het |
| Oprd1 |
A |
G |
4: 131,841,112 (GRCm39) |
I282T |
probably damaging |
Het |
| Or4c103 |
T |
C |
2: 88,513,767 (GRCm39) |
H103R |
possibly damaging |
Het |
| Or5p50 |
T |
C |
7: 107,421,782 (GRCm39) |
N298S |
probably benign |
Het |
| Or6b3 |
A |
T |
1: 92,439,573 (GRCm39) |
M59K |
probably benign |
Het |
| Or6d12 |
A |
G |
6: 116,492,936 (GRCm39) |
Y66C |
probably damaging |
Het |
| Osbp2 |
T |
C |
11: 3,662,134 (GRCm39) |
I240V |
probably damaging |
Het |
| Otub2 |
C |
A |
12: 103,359,163 (GRCm39) |
P84Q |
probably benign |
Het |
| Parp9 |
A |
T |
16: 35,777,360 (GRCm39) |
I435F |
probably benign |
Het |
| Pcdh18 |
C |
T |
3: 49,709,923 (GRCm39) |
R464H |
probably benign |
Het |
| Pcsk6 |
G |
T |
7: 65,675,156 (GRCm39) |
|
probably null |
Het |
| Ptgs2 |
G |
A |
1: 149,978,512 (GRCm39) |
R208Q |
probably benign |
Het |
| Rab11b |
G |
A |
17: 33,968,841 (GRCm39) |
R51C |
probably damaging |
Het |
| Rad1 |
A |
G |
15: 10,493,343 (GRCm39) |
I257V |
probably benign |
Het |
| Rbms3 |
C |
T |
9: 116,415,085 (GRCm39) |
|
probably null |
Het |
| Rxfp2 |
A |
T |
5: 149,983,364 (GRCm39) |
I300L |
probably benign |
Het |
| Rxfp2 |
C |
A |
5: 149,983,368 (GRCm39) |
T301K |
probably benign |
Het |
| Sars2 |
G |
T |
7: 28,443,733 (GRCm39) |
A112S |
probably benign |
Het |
| Scn10a |
T |
C |
9: 119,442,616 (GRCm39) |
D1543G |
probably damaging |
Het |
| Serpinb1b |
A |
G |
13: 33,271,406 (GRCm39) |
H59R |
probably benign |
Het |
| Sgsm2 |
T |
A |
11: 74,745,319 (GRCm39) |
D661V |
possibly damaging |
Het |
| Smad6 |
C |
A |
9: 63,927,688 (GRCm39) |
V207L |
probably damaging |
Het |
| Son |
TCCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCAGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
TCCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,457,183 (GRCm39) |
|
probably benign |
Het |
| Tenm2 |
C |
T |
11: 35,939,956 (GRCm39) |
R1390Q |
probably damaging |
Het |
| Tmem132a |
T |
A |
19: 10,844,295 (GRCm39) |
Q101L |
probably damaging |
Het |
| Tmem151a |
A |
G |
19: 5,132,801 (GRCm39) |
V135A |
probably damaging |
Het |
| Trappc10 |
T |
C |
10: 78,046,262 (GRCm39) |
K443E |
probably damaging |
Het |
| Trrap |
A |
T |
5: 144,779,517 (GRCm39) |
N3161I |
possibly damaging |
Het |
| Tspan32 |
G |
T |
7: 142,558,863 (GRCm39) |
R6L |
possibly damaging |
Het |
| Tut7 |
C |
G |
13: 59,936,364 (GRCm39) |
D1246H |
probably damaging |
Het |
| Ugt2a2 |
T |
C |
5: 87,608,468 (GRCm39) |
D457G |
possibly damaging |
Het |
| Ulk2 |
A |
T |
11: 61,725,657 (GRCm39) |
S140T |
possibly damaging |
Het |
| Upf1 |
C |
T |
8: 70,792,695 (GRCm39) |
A338T |
possibly damaging |
Het |
| Usp43 |
C |
T |
11: 67,774,110 (GRCm39) |
R460Q |
probably null |
Het |
| Uxs1 |
A |
G |
1: 43,856,118 (GRCm39) |
|
probably benign |
Het |
| Vmn1r59 |
A |
G |
7: 5,457,725 (GRCm39) |
C12R |
probably damaging |
Het |
| Wdr64 |
A |
G |
1: 175,617,499 (GRCm39) |
D693G |
probably benign |
Het |
| Wnk1 |
A |
T |
6: 119,920,839 (GRCm39) |
|
probably null |
Het |
| Wnt2 |
G |
T |
6: 18,028,046 (GRCm39) |
R63S |
probably benign |
Het |
| Zfp418 |
A |
T |
7: 7,184,562 (GRCm39) |
Q175L |
probably benign |
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 |
|
R7203:Spata31h1
|
UTSW |
10 |
82,129,248 (GRCm39) |
missense |
probably benign |
0.00 |
|
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'- TCGGTTTTGGGTGCCATAAC -3'
(R):5'- TTCTGGACTAAAAGCCACAAATCAG -3'
Sequencing Primer
(F):5'- GACTCCAGTCACAGGGTTTC -3'
(R):5'- TCAGAAGCAAGATGGGAAGCCTC -3'
|
| Posted On |
2019-06-26 |
Incidental Mutation