Incidental Mutation 'R7560:Spata31h1'
| ID |
585047 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Spata31h1
|
| Ensembl Gene |
ENSMUSG00000044581 |
| Gene Name |
SPATA31 subfamily H member 1 |
| Synonyms |
4932415D10Rik |
| MMRRC Submission |
045626-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.072)
|
| Stock # |
R7560 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
10 |
| Chromosomal Location |
82117950-82152416 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 82120449 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tyrosine to Cysteine
at position 4187
(Y4187C)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000151425
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000171401]
[ENSMUST00000217661]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000171401
AA Change: Y217C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000126178
Gene: ENSMUSG00000044581
AA Change: Y217C
| 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 damaging
Transcript: ENSMUST00000217661
AA Change: Y4187C
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.4%
|
| Validation Efficiency |
100% (100/100) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 101 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Acot12 |
A |
G |
13: 91,932,510 (GRCm39) |
D502G |
probably benign |
Het |
| Adrb1 |
T |
C |
19: 56,711,120 (GRCm39) |
V106A |
probably damaging |
Het |
| Ahcyl2 |
G |
T |
6: 29,886,139 (GRCm39) |
G352W |
probably damaging |
Het |
| Ahnak2 |
T |
G |
12: 112,745,851 (GRCm39) |
D446A |
|
Het |
| Arhgap42 |
T |
C |
9: 9,035,532 (GRCm39) |
D270G |
probably benign |
Het |
| Atp2a1 |
A |
G |
7: 126,058,828 (GRCm39) |
V129A |
possibly damaging |
Het |
| B9d2 |
G |
A |
7: 25,380,784 (GRCm39) |
|
probably benign |
Het |
| Bace1 |
A |
T |
9: 45,767,437 (GRCm39) |
I207F |
possibly damaging |
Het |
| Blnk |
T |
A |
19: 40,940,834 (GRCm39) |
I190F |
possibly damaging |
Het |
| Bmp7 |
C |
T |
2: 172,781,757 (GRCm39) |
E36K |
possibly damaging |
Het |
| Brsk2 |
A |
G |
7: 141,554,597 (GRCm39) |
E654G |
probably benign |
Het |
| Cacna2d3 |
T |
C |
14: 28,780,378 (GRCm39) |
H661R |
probably benign |
Het |
| Cdh4 |
T |
C |
2: 179,532,695 (GRCm39) |
V719A |
probably benign |
Het |
| Cdkn2d |
G |
T |
9: 21,200,540 (GRCm39) |
P77H |
probably damaging |
Het |
| Chd3 |
A |
G |
11: 69,247,096 (GRCm39) |
V1024A |
probably damaging |
Het |
| Chsy1 |
T |
A |
7: 65,820,992 (GRCm39) |
M409K |
possibly damaging |
Het |
| Chsy1 |
T |
C |
7: 65,821,319 (GRCm39) |
L518P |
probably damaging |
Het |
| Cic |
G |
A |
7: 24,972,278 (GRCm39) |
V670M |
probably damaging |
Het |
| Clock |
A |
T |
5: 76,390,738 (GRCm39) |
|
probably null |
Het |
| Coro1a |
C |
A |
7: 126,302,306 (GRCm39) |
V14L |
probably damaging |
Het |
| Ctcfl |
C |
A |
2: 172,960,199 (GRCm39) |
C128F |
probably damaging |
Het |
| Cyb5b |
A |
G |
8: 107,896,491 (GRCm39) |
T71A |
probably damaging |
Het |
| Cyp2c40 |
C |
G |
19: 39,795,658 (GRCm39) |
V174L |
possibly damaging |
Het |
| D630045J12Rik |
T |
A |
6: 38,173,562 (GRCm39) |
Q202L |
possibly damaging |
Het |
| Dgkz |
T |
C |
2: 91,773,160 (GRCm39) |
|
probably benign |
Het |
| Dlgap2 |
T |
C |
8: 14,872,697 (GRCm39) |
|
probably null |
Het |
| Dnah1 |
T |
C |
14: 31,026,940 (GRCm39) |
I695V |
probably benign |
Het |
| Dst |
T |
A |
1: 34,221,532 (GRCm39) |
S2445R |
possibly damaging |
Het |
| Elob |
T |
C |
17: 24,043,950 (GRCm39) |
D83G |
probably benign |
Het |
| Elp4 |
T |
A |
2: 105,624,933 (GRCm39) |
D320V |
probably damaging |
Het |
| Enpp5 |
G |
A |
17: 44,396,155 (GRCm39) |
G356S |
probably damaging |
Het |
| Etfdh |
T |
C |
3: 79,530,886 (GRCm39) |
Y45C |
probably damaging |
Het |
| Exph5 |
A |
G |
9: 53,287,073 (GRCm39) |
I1385V |
probably benign |
Het |
| Fat3 |
A |
T |
9: 15,908,138 (GRCm39) |
D2621E |
probably damaging |
Het |
| Fbxl6 |
G |
T |
15: 76,422,669 (GRCm39) |
A83D |
probably benign |
Het |
| Fmo2 |
A |
G |
1: 162,716,318 (GRCm39) |
Y90H |
probably damaging |
Het |
| Fzd4 |
T |
A |
7: 89,056,761 (GRCm39) |
Y269* |
probably null |
Het |
| Grik5 |
T |
A |
7: 24,757,951 (GRCm39) |
I377F |
probably damaging |
Het |
| Havcr2 |
C |
A |
11: 46,349,889 (GRCm39) |
P137Q |
probably damaging |
Het |
| Hectd4 |
A |
G |
5: 121,392,405 (GRCm39) |
N223S |
possibly damaging |
Het |
| Hmcn2 |
A |
G |
2: 31,347,185 (GRCm39) |
S4792G |
probably benign |
Het |
| Hps3 |
T |
G |
3: 20,084,616 (GRCm39) |
I191L |
probably benign |
Het |
| Ica1l |
T |
A |
1: 60,049,369 (GRCm39) |
K195* |
probably null |
Het |
| Idh2 |
TCCCAGGGCC |
TCC |
7: 79,748,079 (GRCm39) |
|
probably null |
Het |
| Ift140 |
A |
G |
17: 25,311,315 (GRCm39) |
D1170G |
probably benign |
Het |
| Igflr1 |
T |
C |
7: 30,266,776 (GRCm39) |
F208S |
possibly damaging |
Het |
| Kcnma1 |
T |
C |
14: 23,580,310 (GRCm39) |
T313A |
probably benign |
Het |
| Krt6a |
T |
A |
15: 101,598,994 (GRCm39) |
I524F |
unknown |
Het |
| Lce1d |
G |
T |
3: 92,593,148 (GRCm39) |
H88Q |
unknown |
Het |
| Lrmda |
A |
G |
14: 22,878,770 (GRCm39) |
E177G |
probably benign |
Het |
| Lrrn3 |
T |
A |
12: 41,502,712 (GRCm39) |
N535I |
possibly damaging |
Het |
| Map2k4 |
T |
A |
11: 65,666,583 (GRCm39) |
I40L |
unknown |
Het |
| Map7d1 |
A |
G |
4: 126,130,429 (GRCm39) |
L459P |
probably damaging |
Het |
| Mipol1 |
A |
T |
12: 57,352,859 (GRCm39) |
N66I |
possibly damaging |
Het |
| Mycn |
A |
C |
12: 12,990,292 (GRCm39) |
F35V |
probably benign |
Het |
| Mzt2 |
A |
C |
16: 15,680,669 (GRCm39) |
M40R |
possibly damaging |
Het |
| N4bp2 |
T |
G |
5: 65,948,458 (GRCm39) |
L363V |
probably damaging |
Het |
| Nfat5 |
T |
A |
8: 108,097,221 (GRCm39) |
M1532K |
probably benign |
Het |
| Notch1 |
G |
A |
2: 26,350,177 (GRCm39) |
T2321M |
probably benign |
Het |
| Nr1h4 |
T |
C |
10: 89,334,123 (GRCm39) |
D89G |
probably benign |
Het |
| Nsun4 |
G |
A |
4: 115,908,691 (GRCm39) |
T623I |
possibly damaging |
Het |
| Nup155 |
T |
C |
15: 8,184,531 (GRCm39) |
S1309P |
probably benign |
Het |
| Or4e1 |
T |
C |
14: 52,700,851 (GRCm39) |
N205S |
probably damaging |
Het |
| Or51f5 |
T |
C |
7: 102,430,889 (GRCm39) |
S69P |
probably damaging |
Het |
| Or8h10 |
T |
C |
2: 86,809,122 (GRCm39) |
Y6C |
probably benign |
Het |
| Pcsk5 |
A |
G |
19: 17,814,336 (GRCm39) |
F61L |
probably benign |
Het |
| Phrf1 |
A |
T |
7: 140,811,138 (GRCm39) |
|
probably null |
Het |
| Pkd1 |
G |
A |
17: 24,792,605 (GRCm39) |
E1431K |
probably benign |
Het |
| Pkd2 |
T |
A |
5: 104,628,219 (GRCm39) |
I431N |
probably damaging |
Het |
| Plcb2 |
A |
G |
2: 118,546,124 (GRCm39) |
L557P |
probably damaging |
Het |
| Poteg |
A |
G |
8: 27,984,988 (GRCm39) |
N449S |
probably benign |
Het |
| Ppargc1b |
C |
A |
18: 61,445,281 (GRCm39) |
G192W |
probably damaging |
Het |
| Rab13 |
T |
C |
3: 90,132,206 (GRCm39) |
S178P |
probably benign |
Het |
| Ralgds |
A |
G |
2: 28,437,607 (GRCm39) |
D571G |
probably damaging |
Het |
| Ror2 |
A |
G |
13: 53,264,849 (GRCm39) |
S748P |
probably benign |
Het |
| Sart1 |
A |
T |
19: 5,434,905 (GRCm39) |
L167Q |
probably damaging |
Het |
| Septin12 |
A |
G |
16: 4,810,055 (GRCm39) |
V160A |
possibly damaging |
Het |
| Sgo1 |
T |
C |
17: 53,986,295 (GRCm39) |
S299G |
probably benign |
Het |
| Shoc1 |
T |
C |
4: 59,076,140 (GRCm39) |
N601S |
possibly damaging |
Het |
| Slc35b4 |
T |
A |
6: 34,140,296 (GRCm39) |
D152V |
probably benign |
Het |
| Specc1 |
T |
A |
11: 62,019,235 (GRCm39) |
|
probably null |
Het |
| Synj1 |
G |
A |
16: 90,737,371 (GRCm39) |
T1308I |
probably benign |
Het |
| Thap12 |
T |
G |
7: 98,359,438 (GRCm39) |
L106V |
probably damaging |
Het |
| Togaram1 |
T |
C |
12: 65,057,916 (GRCm39) |
M1501T |
possibly damaging |
Het |
| Top2a |
G |
T |
11: 98,891,663 (GRCm39) |
N1153K |
probably benign |
Het |
| Trpm5 |
A |
G |
7: 142,634,723 (GRCm39) |
L658P |
probably damaging |
Het |
| Ttc21b |
G |
A |
2: 66,047,548 (GRCm39) |
A849V |
possibly damaging |
Het |
| Vcf1 |
C |
T |
11: 113,554,215 (GRCm39) |
G160D |
probably damaging |
Het |
| Vmn1r80 |
A |
T |
7: 11,927,750 (GRCm39) |
I287F |
probably damaging |
Het |
| Vmn1r87 |
T |
C |
7: 12,865,745 (GRCm39) |
S181G |
probably damaging |
Het |
| Vmn2r71 |
A |
T |
7: 85,273,115 (GRCm39) |
H643L |
probably benign |
Het |
| Washc5 |
G |
A |
15: 59,238,041 (GRCm39) |
R228C |
probably damaging |
Het |
| Wdr72 |
T |
C |
9: 74,117,408 (GRCm39) |
S719P |
probably damaging |
Het |
| Xrcc3 |
G |
T |
12: 111,774,336 (GRCm39) |
D164E |
probably benign |
Het |
| Zc2hc1b |
G |
A |
10: 13,044,529 (GRCm39) |
R45C |
probably damaging |
Het |
| Zfp335 |
A |
G |
2: 164,737,912 (GRCm39) |
Y900H |
probably damaging |
Het |
| Zfp512b |
G |
A |
2: 181,228,875 (GRCm39) |
R697C |
probably damaging |
Het |
| Zfp60 |
T |
C |
7: 27,448,561 (GRCm39) |
Y410H |
probably damaging |
Het |
| Zfp60 |
T |
A |
7: 27,448,696 (GRCm39) |
C455S |
probably damaging |
Het |
| Zfp605 |
C |
T |
5: 110,275,157 (GRCm39) |
Q92* |
probably null |
Het |
| Zfp64 |
C |
T |
2: 168,767,585 (GRCm39) |
D676N |
probably damaging |
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 |
|
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 |
|
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'- GGACAAGACCTGACTCTAGAGG -3'
(R):5'- ACACGTGGCTCAACATCTTC -3'
Sequencing Primer
(F):5'- CAGAGGAACATTGTGGGGTATTTGAC -3'
(R):5'- CGTGGCTCAACATCTTCTATAATAC -3'
|
| Posted On |
2019-10-17 |
Incidental Mutation