Incidental Mutation 'R4857:Spata31h1'
| ID |
374074 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Spata31h1
|
| Ensembl Gene |
ENSMUSG00000044581 |
| Gene Name |
SPATA31 subfamily H member 1 |
| Synonyms |
4932415D10Rik |
| MMRRC Submission |
042468-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.072)
|
| Stock # |
R4857 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
10 |
| Chromosomal Location |
82117950-82152416 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 82119682 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Alanine
at position 4443
(T4443A)
|
| 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
AA Change: T473A
PolyPhen 2
Score 0.130 (Sensitivity: 0.93; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000126178
Gene: ENSMUSG00000044581
AA Change: T473A
| 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 |
possibly damaging
Transcript: ENSMUST00000217661
AA Change: T4443A
PolyPhen 2
Score 0.610 (Sensitivity: 0.87; Specificity: 0.91)
|
| Meta Mutation Damage Score |
0.1795 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.3%
- 20x: 92.3%
|
| Validation Efficiency |
97% (115/119) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 101 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930548G14Rik |
C |
T |
15: 46,488,927 (GRCm39) |
|
noncoding transcript |
Het |
| Aasdh |
A |
T |
5: 77,035,131 (GRCm39) |
F428L |
probably benign |
Het |
| Abca13 |
A |
G |
11: 9,244,143 (GRCm39) |
N2002S |
probably benign |
Het |
| Acot7 |
T |
G |
4: 152,322,211 (GRCm39) |
F248V |
possibly damaging |
Het |
| Acsf2 |
A |
G |
11: 94,460,164 (GRCm39) |
I396T |
probably benign |
Het |
| Agbl1 |
A |
G |
7: 76,069,583 (GRCm39) |
N372D |
probably benign |
Het |
| Ahctf1 |
A |
T |
1: 179,626,922 (GRCm39) |
|
probably benign |
Het |
| Akap11 |
T |
C |
14: 78,736,300 (GRCm39) |
D1830G |
|
Het |
| Bcl7b |
A |
G |
5: 135,202,033 (GRCm39) |
*59W |
probably null |
Het |
| Bdh1 |
A |
G |
16: 31,266,366 (GRCm39) |
|
probably null |
Het |
| Bin3 |
A |
G |
14: 70,366,344 (GRCm39) |
N69S |
probably benign |
Het |
| Bltp3b |
A |
T |
10: 89,615,825 (GRCm39) |
N156I |
probably damaging |
Het |
| Bsdc1 |
T |
C |
4: 129,365,685 (GRCm39) |
|
probably benign |
Het |
| Cacna1i |
T |
C |
15: 80,253,863 (GRCm39) |
V700A |
probably damaging |
Het |
| Calcr |
T |
C |
6: 3,708,511 (GRCm39) |
N225S |
probably benign |
Het |
| Cby2 |
C |
T |
14: 75,830,478 (GRCm39) |
E8K |
probably damaging |
Het |
| Cdh23 |
A |
G |
10: 60,227,563 (GRCm39) |
S1173P |
probably damaging |
Het |
| Cftr |
C |
T |
6: 18,320,974 (GRCm39) |
T1428M |
possibly damaging |
Het |
| Chd1l |
T |
C |
3: 97,479,975 (GRCm39) |
K591E |
probably benign |
Het |
| Chrd |
C |
T |
16: 20,557,508 (GRCm39) |
P709L |
possibly damaging |
Het |
| Ckap4 |
T |
C |
10: 84,369,352 (GRCm39) |
R127G |
possibly damaging |
Het |
| Cnbd2 |
T |
C |
2: 156,209,485 (GRCm39) |
F476S |
probably benign |
Het |
| Dclk3 |
T |
C |
9: 111,297,716 (GRCm39) |
V420A |
probably benign |
Het |
| Dnah5 |
A |
G |
15: 28,345,953 (GRCm39) |
D2431G |
probably benign |
Het |
| Duox1 |
T |
A |
2: 122,146,212 (GRCm39) |
I10N |
probably benign |
Het |
| Ece2 |
T |
A |
16: 20,436,556 (GRCm39) |
V126D |
probably damaging |
Het |
| Elfn1 |
T |
C |
5: 139,958,840 (GRCm39) |
Y615H |
probably damaging |
Het |
| Epha1 |
T |
C |
6: 42,338,416 (GRCm39) |
D720G |
probably benign |
Het |
| Fras1 |
A |
G |
5: 96,926,018 (GRCm39) |
I3741V |
probably benign |
Het |
| Gm53 |
A |
T |
11: 96,142,562 (GRCm39) |
|
noncoding transcript |
Het |
| Grb10 |
G |
T |
11: 11,901,469 (GRCm39) |
|
probably benign |
Het |
| Grid2ip |
A |
G |
5: 143,368,384 (GRCm39) |
H568R |
probably damaging |
Het |
| Gsap |
A |
T |
5: 21,492,797 (GRCm39) |
|
probably null |
Het |
| Gse1 |
T |
C |
8: 121,299,496 (GRCm39) |
|
probably benign |
Het |
| Gstm1 |
T |
C |
3: 107,923,724 (GRCm39) |
R94G |
possibly damaging |
Het |
| Gtf2ird1 |
A |
G |
5: 134,391,398 (GRCm39) |
F866L |
probably damaging |
Het |
| Haao |
T |
A |
17: 84,146,009 (GRCm39) |
|
probably null |
Het |
| Hcn4 |
A |
T |
9: 58,766,853 (GRCm39) |
I805F |
unknown |
Het |
| Hemk1 |
A |
T |
9: 107,206,647 (GRCm39) |
|
probably benign |
Het |
| Il12rb1 |
A |
T |
8: 71,263,232 (GRCm39) |
Y33F |
possibly damaging |
Het |
| Il19 |
T |
A |
1: 130,863,683 (GRCm39) |
I103F |
probably damaging |
Het |
| Itpr1 |
A |
G |
6: 108,387,828 (GRCm39) |
N1522S |
probably benign |
Het |
| Klhdc8a |
A |
G |
1: 132,230,843 (GRCm39) |
Y236C |
probably damaging |
Het |
| Klhl3 |
C |
T |
13: 58,166,620 (GRCm39) |
G404S |
probably damaging |
Het |
| Large2 |
T |
C |
2: 92,196,979 (GRCm39) |
|
probably benign |
Het |
| Lgi1 |
C |
A |
19: 38,294,698 (GRCm39) |
A490E |
probably damaging |
Het |
| Lmbr1 |
A |
G |
5: 29,528,807 (GRCm39) |
L112P |
probably damaging |
Het |
| Lmo7 |
T |
A |
14: 102,124,784 (GRCm39) |
|
probably null |
Het |
| Lpin1 |
A |
C |
12: 16,613,631 (GRCm39) |
I479S |
possibly damaging |
Het |
| Lrrc40 |
T |
A |
3: 157,771,866 (GRCm39) |
|
probably benign |
Het |
| Lrrc9 |
A |
G |
12: 72,546,466 (GRCm39) |
N1218S |
possibly damaging |
Het |
| Map3k9 |
A |
G |
12: 81,771,401 (GRCm39) |
V729A |
probably benign |
Het |
| Marf1 |
A |
T |
16: 13,946,475 (GRCm39) |
Y1215* |
probably null |
Het |
| Moap1 |
T |
A |
12: 102,708,824 (GRCm39) |
I242L |
probably benign |
Het |
| Mpo |
A |
G |
11: 87,687,107 (GRCm39) |
K218E |
probably benign |
Het |
| Mpz |
C |
T |
1: 170,986,379 (GRCm39) |
R98C |
probably damaging |
Het |
| Neb |
T |
G |
2: 52,091,992 (GRCm39) |
K5024T |
probably damaging |
Het |
| Nlrp4b |
C |
T |
7: 10,449,225 (GRCm39) |
T109I |
probably benign |
Het |
| Noc3l |
T |
A |
19: 38,781,244 (GRCm39) |
|
probably null |
Het |
| Nosip |
G |
A |
7: 44,726,102 (GRCm39) |
V220I |
probably benign |
Het |
| Nyap1 |
A |
C |
5: 137,733,840 (GRCm39) |
S398A |
probably damaging |
Het |
| Or12d17 |
A |
G |
17: 37,777,714 (GRCm39) |
M206V |
possibly damaging |
Het |
| Or4a68 |
T |
G |
2: 89,269,967 (GRCm39) |
I219L |
probably damaging |
Het |
| Or4f54 |
A |
G |
2: 111,123,488 (GRCm39) |
N292D |
possibly damaging |
Het |
| Osbpl7 |
T |
C |
11: 96,947,495 (GRCm39) |
|
probably benign |
Het |
| Pard3 |
A |
T |
8: 128,050,535 (GRCm39) |
Y199F |
probably damaging |
Het |
| Pcdha11 |
G |
A |
18: 37,144,505 (GRCm39) |
V199I |
probably benign |
Het |
| Pcdhga8 |
A |
T |
18: 37,859,967 (GRCm39) |
N341I |
probably damaging |
Het |
| Pcsk4 |
A |
G |
10: 80,160,873 (GRCm39) |
S318P |
probably damaging |
Het |
| Phldb1 |
C |
A |
9: 44,607,389 (GRCm39) |
R1272L |
probably damaging |
Het |
| Phlpp2 |
A |
G |
8: 110,603,642 (GRCm39) |
T103A |
probably damaging |
Het |
| Pibf1 |
T |
A |
14: 99,423,937 (GRCm39) |
Y503* |
probably null |
Het |
| Pkn1 |
A |
T |
8: 84,410,856 (GRCm39) |
|
probably null |
Het |
| Pramel22 |
A |
T |
4: 143,383,158 (GRCm39) |
N20K |
possibly damaging |
Het |
| Ptprf |
A |
G |
4: 118,074,394 (GRCm39) |
|
probably benign |
Het |
| Rbm19 |
C |
A |
5: 120,270,898 (GRCm39) |
|
probably benign |
Het |
| Rcan1 |
T |
C |
16: 92,262,794 (GRCm39) |
D5G |
possibly damaging |
Het |
| Recql5 |
A |
T |
11: 115,819,038 (GRCm39) |
L176Q |
probably damaging |
Het |
| Rev3l |
T |
A |
10: 39,714,455 (GRCm39) |
L2393Q |
probably damaging |
Het |
| Rp1 |
C |
A |
1: 4,422,539 (GRCm39) |
K180N |
probably damaging |
Het |
| Rp1 |
T |
A |
1: 4,422,540 (GRCm39) |
K180M |
probably damaging |
Het |
| Sdk1 |
T |
C |
5: 142,147,531 (GRCm39) |
V1461A |
probably benign |
Het |
| Sdk2 |
A |
T |
11: 113,712,208 (GRCm39) |
L1653* |
probably null |
Het |
| Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
| Skint10 |
A |
T |
4: 112,603,830 (GRCm39) |
V119D |
possibly damaging |
Het |
| Sncaip |
T |
C |
18: 53,002,297 (GRCm39) |
S273P |
probably benign |
Het |
| Sp1 |
T |
G |
15: 102,339,409 (GRCm39) |
I449S |
probably damaging |
Het |
| Spats2 |
T |
C |
15: 99,072,301 (GRCm39) |
L78P |
probably damaging |
Het |
| Stambp |
T |
A |
6: 83,533,348 (GRCm39) |
N305I |
probably benign |
Het |
| Stim2 |
A |
T |
5: 54,275,888 (GRCm39) |
S688C |
probably damaging |
Het |
| Sytl3 |
A |
G |
17: 7,003,980 (GRCm39) |
N355S |
probably damaging |
Het |
| Taf4b |
C |
T |
18: 14,937,635 (GRCm39) |
A236V |
probably null |
Het |
| Tnfaip6 |
A |
G |
2: 51,941,086 (GRCm39) |
|
probably null |
Het |
| Trpc2 |
T |
A |
7: 101,733,176 (GRCm39) |
S416T |
probably benign |
Het |
| Ttn |
T |
C |
2: 76,569,210 (GRCm39) |
T27228A |
probably damaging |
Het |
| Ush2a |
T |
A |
1: 188,269,917 (GRCm39) |
D1721E |
probably benign |
Het |
| Usp47 |
T |
A |
7: 111,681,759 (GRCm39) |
H523Q |
probably damaging |
Het |
| Vmn1r8 |
A |
T |
6: 57,013,338 (GRCm39) |
I130F |
probably benign |
Het |
| Vps13b |
A |
G |
15: 35,456,800 (GRCm39) |
S749G |
probably benign |
Het |
| Xrcc5 |
C |
A |
1: 72,365,424 (GRCm39) |
T283K |
possibly damaging |
Het |
| Ydjc |
A |
G |
16: 16,966,002 (GRCm39) |
|
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 |
|
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 |
|
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'- GCTTGGAATGCCTGCCTTAG -3'
(R):5'- CTGCTTCTGTACAAGTCCACAC -3'
Sequencing Primer
(F):5'- CCTTAGGCTATGAAAAAGCAGTTG -3'
(R):5'- TGTACAAGTCCACACGCAGC -3'
|
| Posted On |
2016-03-01 |
Incidental Mutation