Incidental Mutation 'FR4737:Stard9'
| ID |
511582 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Stard9
|
| Ensembl Gene |
ENSMUSG00000033705 |
| Gene Name |
StAR related lipid transfer domain containing 9 |
| Synonyms |
4831403C07Rik, E230025N21Rik, Kif16a, N-3 kinesin |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.173)
|
| Stock # |
FR4737 ()
|
| Quality Score |
217.468 |
|
Status
|
Not validated
|
| Chromosome |
2 |
| Chromosomal Location |
120459602-120562376 bp(+) (GRCm39) |
| Type of Mutation |
small insertion (5 aa in frame mutation) |
| DNA Base Change (assembly) |
C to CTAAGGGACTAGTAGG
at 120526566 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000136055
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000140843]
[ENSMUST00000180041]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000140843
|
| SMART Domains |
Protein: ENSMUSP00000117178
Gene: ENSMUSG00000033705
| Domain | Start | End | E-Value | Type |
|---|
|
FHA
|
63 |
115 |
2.8e-4 |
SMART |
|
coiled coil region
|
334 |
354 |
N/A |
INTRINSIC |
|
low complexity region
|
573 |
584 |
N/A |
INTRINSIC |
|
low complexity region
|
866 |
871 |
N/A |
INTRINSIC |
|
low complexity region
|
1023 |
1035 |
N/A |
INTRINSIC |
|
low complexity region
|
1234 |
1248 |
N/A |
INTRINSIC |
|
low complexity region
|
1765 |
1775 |
N/A |
INTRINSIC |
|
low complexity region
|
2546 |
2559 |
N/A |
INTRINSIC |
|
low complexity region
|
2953 |
2963 |
N/A |
INTRINSIC |
|
low complexity region
|
3269 |
3281 |
N/A |
INTRINSIC |
|
low complexity region
|
3421 |
3435 |
N/A |
INTRINSIC |
|
coiled coil region
|
3767 |
3808 |
N/A |
INTRINSIC |
|
low complexity region
|
3812 |
3821 |
N/A |
INTRINSIC |
|
low complexity region
|
3827 |
3844 |
N/A |
INTRINSIC |
|
low complexity region
|
3904 |
3925 |
N/A |
INTRINSIC |
|
SCOP:d1jssa_
|
3946 |
4142 |
1e-28 |
SMART |
|
Blast:START
|
3947 |
4143 |
1e-10 |
BLAST |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000180041
|
| SMART Domains |
Protein: ENSMUSP00000136055
Gene: ENSMUSG00000033705
| Domain | Start | End | E-Value | Type |
|---|
|
KISc
|
1 |
392 |
3.31e-143 |
SMART |
|
low complexity region
|
398 |
409 |
N/A |
INTRINSIC |
|
FHA
|
481 |
533 |
2.8e-4 |
SMART |
|
coiled coil region
|
752 |
772 |
N/A |
INTRINSIC |
|
low complexity region
|
991 |
1002 |
N/A |
INTRINSIC |
|
low complexity region
|
1284 |
1289 |
N/A |
INTRINSIC |
|
low complexity region
|
1441 |
1453 |
N/A |
INTRINSIC |
|
low complexity region
|
1652 |
1666 |
N/A |
INTRINSIC |
|
low complexity region
|
2183 |
2193 |
N/A |
INTRINSIC |
|
low complexity region
|
2964 |
2977 |
N/A |
INTRINSIC |
|
low complexity region
|
3371 |
3381 |
N/A |
INTRINSIC |
|
low complexity region
|
3687 |
3699 |
N/A |
INTRINSIC |
|
low complexity region
|
3839 |
3853 |
N/A |
INTRINSIC |
|
coiled coil region
|
4185 |
4226 |
N/A |
INTRINSIC |
|
low complexity region
|
4230 |
4239 |
N/A |
INTRINSIC |
|
low complexity region
|
4245 |
4262 |
N/A |
INTRINSIC |
|
low complexity region
|
4322 |
4343 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 99.8%
- 3x: 99.6%
- 10x: 98.8%
- 20x: 97.0%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 211 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700001K19Rik |
TCT |
TCTCCT |
12: 110,634,882 (GRCm39) |
|
probably benign |
Het |
| A630001G21Rik |
CTGTT |
CT |
1: 85,650,856 (GRCm39) |
|
probably benign |
Homo |
| Abcb11 |
C |
A |
2: 69,073,862 (GRCm39) |
R1221L |
probably damaging |
Homo |
| Abcb4 |
GAAA |
G |
5: 8,946,597 (GRCm39) |
|
probably benign |
Homo |
| Ahdc1 |
CT |
CTCGT |
4: 132,790,070 (GRCm39) |
|
probably benign |
Homo |
| Alpk3 |
TCT |
TCTACT |
7: 80,727,510 (GRCm39) |
|
probably benign |
Het |
| Amfr |
C |
G |
8: 94,731,787 (GRCm39) |
G30R |
probably damaging |
Homo |
| Ankrd35 |
GC |
GCTAC |
3: 96,591,165 (GRCm39) |
|
probably benign |
Homo |
| Anxa7 |
C |
T |
14: 20,519,479 (GRCm39) |
G113E |
probably damaging |
Homo |
| Apc |
CAATAAAGC |
CAATAAAGCTAATAAAGC |
18: 34,415,052 (GRCm39) |
|
probably benign |
Homo |
| Apol6 |
GTTT |
GTTTCTTT |
15: 76,935,642 (GRCm39) |
|
probably null |
Homo |
| Arpc1b |
GGTGGC |
GGTGGCGTGGC |
5: 145,063,597 (GRCm39) |
|
probably null |
Het |
| AY358078 |
C |
T |
14: 52,043,155 (GRCm39) |
S281L |
unknown |
Homo |
| Blm |
ACCTGC |
ACCTGCCTGC |
7: 80,113,519 (GRCm39) |
|
probably null |
Het |
| Blm |
T |
TACCA |
7: 80,113,522 (GRCm39) |
|
probably null |
Het |
| Bltp1 |
TTATTAT |
TTATTATTATTATTACTATTAT |
3: 37,104,903 (GRCm39) |
|
probably benign |
Het |
| Blzf1 |
TTGT |
TT |
1: 164,131,486 (GRCm39) |
|
probably null |
Homo |
| Btnl10 |
A |
AAGG |
11: 58,814,757 (GRCm39) |
|
probably benign |
Homo |
| Cacna1a |
ACC |
ACCGCC |
8: 85,365,349 (GRCm39) |
|
probably benign |
Het |
| Cacna1a |
ACC |
ACCCCC |
8: 85,365,355 (GRCm39) |
|
probably benign |
Homo |
| Catsper2 |
TTC |
TTCTTTTACTTTGTC |
2: 121,228,021 (GRCm39) |
|
probably benign |
Homo |
| Ccdc170 |
ACC |
ACCTCC |
10: 4,511,023 (GRCm39) |
|
probably benign |
Het |
| Ccdc170 |
AC |
ACCCC |
10: 4,511,029 (GRCm39) |
|
probably benign |
Het |
| Ccdc73 |
TAAG |
T |
2: 104,822,185 (GRCm39) |
|
probably benign |
Homo |
| Ccnk |
TTCCCAC |
T |
12: 108,168,766 (GRCm39) |
|
probably benign |
Het |
| Cdan1 |
A |
C |
2: 120,555,452 (GRCm39) |
V763G |
probably damaging |
Het |
| Cdk6 |
A |
G |
5: 3,394,211 (GRCm39) |
|
probably benign |
Het |
| Cdx1 |
TGCTGC |
TGCTGCCGCTGC |
18: 61,152,946 (GRCm39) |
|
probably benign |
Het |
| Cdx1 |
GCTGCT |
GCTGCTTCTGCT |
18: 61,152,950 (GRCm39) |
|
probably benign |
Het |
| Cfap46 |
CCTTCT |
CCTTCTTCT |
7: 139,218,846 (GRCm39) |
|
probably benign |
Homo |
| Chd4 |
GC |
GCTCCCCC |
6: 125,099,094 (GRCm39) |
|
probably benign |
Homo |
| Cluh |
GAGCCT |
GAGCCTAAGCCT |
11: 74,560,350 (GRCm39) |
|
probably benign |
Het |
| Cluh |
CC |
CCTGAGGC |
11: 74,560,359 (GRCm39) |
|
probably benign |
Het |
| Cluh |
CCCCGAGCC |
CCCCGAGCCCGAGCC |
11: 74,560,340 (GRCm39) |
|
probably benign |
Het |
| Cluh |
AGCCTG |
AGCCTGCGCCTG |
11: 74,560,345 (GRCm39) |
|
probably benign |
Het |
| Cntnap1 |
GCCCCA |
GCCCCACCCCCA |
11: 101,080,408 (GRCm39) |
|
probably benign |
Het |
| Cntnap1 |
CCCAGC |
CCCAGCGCCAGC |
11: 101,080,416 (GRCm39) |
|
probably benign |
Het |
| Cntnap1 |
AGCCCC |
AGCCCCCGCCCC |
11: 101,080,395 (GRCm39) |
|
probably benign |
Het |
| Cntnap1 |
GCCCCA |
GCCCCAACCCCA |
11: 101,080,402 (GRCm39) |
|
probably benign |
Het |
| Cracdl |
T |
A |
1: 37,664,116 (GRCm39) |
E594V |
probably benign |
Homo |
| Cracdl |
C |
A |
1: 37,664,117 (GRCm39) |
E594* |
probably null |
Homo |
| Cul9 |
CTC |
CTCTTC |
17: 46,811,784 (GRCm39) |
|
probably benign |
Het |
| Cul9 |
CTCTTC |
CTCTTCTTC |
17: 46,811,772 (GRCm39) |
|
probably benign |
Het |
| Cyth2 |
C |
A |
7: 45,462,466 (GRCm39) |
S102I |
possibly damaging |
Het |
| Dbr1 |
AGGAGG |
AGGAGGCGGAGG |
9: 99,465,739 (GRCm39) |
|
probably benign |
Het |
| Dbr1 |
GGAGG |
GGAGGACGAGG |
9: 99,465,752 (GRCm39) |
|
probably benign |
Het |
| Dennd2b |
CACCACACTGGGGCAGCCCACACTGGGGCAG |
CCCCACACTGGGGCAG |
7: 109,156,128 (GRCm39) |
|
probably benign |
Het |
| Dhx8 |
GACCGA |
GACCGATACCGA |
11: 101,629,005 (GRCm39) |
|
probably benign |
Homo |
| Dhx8 |
GAGACC |
GAGACCCAGACC |
11: 101,629,015 (GRCm39) |
|
probably benign |
Homo |
| Dhx8 |
CGAGAC |
CGAGACGGAGAC |
11: 101,629,008 (GRCm39) |
|
probably benign |
Homo |
| Dnaaf9 |
CC |
CCTGC |
2: 130,612,672 (GRCm39) |
|
probably benign |
Het |
| Dnah8 |
ACTGCCCCT |
ACT |
17: 30,854,439 (GRCm39) |
|
probably benign |
Het |
| Dnah8 |
CCTCCCG |
C |
17: 30,854,451 (GRCm39) |
|
probably benign |
Homo |
| Dnajb5 |
AGGTG |
A |
4: 42,957,126 (GRCm39) |
|
probably null |
Het |
| Dusp10 |
G |
T |
1: 183,769,253 (GRCm39) |
C73F |
probably damaging |
Homo |
| E4f1 |
CCG |
CCGACG |
17: 24,674,166 (GRCm39) |
|
probably benign |
Homo |
| Eif3a |
TTA |
TTATTATA |
19: 60,763,727 (GRCm39) |
|
probably benign |
Het |
| Fam81b |
TTC |
TTCGTC |
13: 76,419,438 (GRCm39) |
|
probably benign |
Het |
| Fbxo22 |
G |
A |
9: 55,116,666 (GRCm39) |
R56H |
probably damaging |
Het |
| Fcgr1 |
CTTCT |
C |
3: 96,191,820 (GRCm39) |
|
probably null |
Het |
| Fcgr1 |
T |
C |
3: 96,194,410 (GRCm39) |
D159G |
probably benign |
Homo |
| Fmn1 |
CC |
CCTCCTTC |
2: 113,356,129 (GRCm39) |
|
probably benign |
Het |
| Fmn1 |
CCTCCT |
CCTCCTACTCCT |
2: 113,356,123 (GRCm39) |
|
probably benign |
Het |
| Fmn1 |
CC |
CCCCCTGC |
2: 113,356,126 (GRCm39) |
|
probably benign |
Het |
| G530012D18Rik |
GA |
GACAGAGATA |
1: 85,504,899 (GRCm39) |
|
probably null |
Het |
| Gli3 |
G |
A |
13: 15,818,942 (GRCm39) |
R248H |
probably damaging |
Het |
| Gm16503 |
G |
A |
4: 147,625,710 (GRCm39) |
G68E |
unknown |
Het |
| Gm19345 |
GGATGGCAGGTG |
GG |
7: 19,591,527 (GRCm39) |
|
probably null |
Het |
| Gm4340 |
AGC |
AGCTGC |
10: 104,031,958 (GRCm39) |
|
probably benign |
Het |
| Gm4340 |
AG |
AGCGG |
10: 104,031,961 (GRCm39) |
|
probably benign |
Het |
| Gm4340 |
GCA |
GCAACA |
10: 104,031,938 (GRCm39) |
|
probably benign |
Het |
| Gm6309 |
C |
T |
5: 146,104,993 (GRCm39) |
V307I |
probably benign |
Het |
| Gpatch11 |
AAGAGG |
AAGAGGCAGAGG |
17: 79,149,600 (GRCm39) |
|
probably benign |
Het |
| Gpatch11 |
AGGAA |
AGGAAGCGGAA |
17: 79,149,609 (GRCm39) |
|
probably benign |
Het |
| Hoxa10 |
T |
A |
6: 52,211,166 (GRCm39) |
Q250L |
possibly damaging |
Homo |
| Hrh1 |
T |
C |
6: 114,458,084 (GRCm39) |
I455T |
possibly damaging |
Het |
| Hspa1b |
GCGCC |
GC |
17: 35,176,105 (GRCm39) |
|
probably benign |
Homo |
| Iba57 |
GAAA |
GAAAAA |
11: 59,052,331 (GRCm39) |
|
probably null |
Homo |
| Igf1r |
TGGAGC |
TGGAGCTGGAGAGGGAGC |
7: 67,875,929 (GRCm39) |
|
probably benign |
Het |
| Il17rd |
CGG |
CGGAGG |
14: 26,804,637 (GRCm39) |
|
probably benign |
Het |
| Il2 |
TGG |
TGGGGCTTGAAGCGG |
3: 37,179,977 (GRCm39) |
|
probably benign |
Het |
| Il2 |
AGGTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
AGCTGCTGCTGCTGCTGCTGCTGCTG |
3: 37,179,913 (GRCm39) |
|
probably benign |
Het |
| Kcng4 |
G |
T |
8: 120,360,258 (GRCm39) |
Y39* |
probably null |
Homo |
| Klra2 |
G |
GAAATCCACAT |
6: 131,198,815 (GRCm39) |
|
probably null |
Het |
| Kmt2b |
CCTCCT |
CCTCCTTCTCCT |
7: 30,285,792 (GRCm39) |
|
probably benign |
Het |
| Kmt2b |
CCTCCT |
CCTCCTGCTCCT |
7: 30,285,795 (GRCm39) |
|
probably benign |
Het |
| Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,803 (GRCm39) |
|
probably benign |
Het |
| Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,285,791 (GRCm39) |
|
probably benign |
Het |
| Krt10 |
TCCTCC |
TCCTCCGCCTCC |
11: 99,280,099 (GRCm39) |
|
probably benign |
Het |
| Krt10 |
TCCGCC |
TCCGCCGCC |
11: 99,277,023 (GRCm39) |
|
probably benign |
Homo |
| Krt10 |
TCC |
TCCTCCACC |
11: 99,280,105 (GRCm39) |
|
probably benign |
Homo |
| Krtap28-10 |
TCCCACA |
TCCCACACCCACA |
1: 83,019,844 (GRCm39) |
|
probably benign |
Homo |
| Krtap4-2 |
A |
ACAC |
11: 99,525,839 (GRCm39) |
|
probably benign |
Het |
| Krtap9-3 |
AC |
ACAGGTGTCGC |
11: 99,488,830 (GRCm39) |
|
probably benign |
Het |
| Las1l |
AGG |
AGGGGG |
X: 94,984,427 (GRCm39) |
|
probably benign |
Het |
| Las1l |
GAG |
GAGCAG |
X: 94,984,435 (GRCm39) |
|
probably benign |
Het |
| Las1l |
AGG |
AGGCGG |
X: 94,984,433 (GRCm39) |
|
probably benign |
Het |
| Lrit3 |
TGC |
TGCAGC |
3: 129,582,455 (GRCm39) |
|
probably benign |
Het |
| Lrit3 |
AC |
ACATTC |
3: 129,597,562 (GRCm39) |
|
probably null |
Homo |
| Lrit3 |
GCT |
GCTTCT |
3: 129,582,459 (GRCm39) |
|
probably benign |
Het |
| Luzp1 |
A |
AGGTGGCCTCTTCAGT |
4: 136,270,507 (GRCm39) |
|
probably benign |
Het |
| Mamld1 |
AGC |
AGCCGC |
X: 70,162,441 (GRCm39) |
|
probably benign |
Het |
| Mamld1 |
GCA |
GCAACA |
X: 70,162,445 (GRCm39) |
|
probably benign |
Het |
| Mapk8ip3 |
G |
A |
17: 25,121,093 (GRCm39) |
|
probably null |
Homo |
| Mbd1 |
TGTCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC |
TATCTGCATCTGCGTCTTCGTCTGCATCTGCATCTGC |
18: 74,406,644 (GRCm39) |
|
probably benign |
Het |
| Nat8f2 |
T |
A |
6: 85,844,668 (GRCm39) |
L231F |
possibly damaging |
Homo |
| Nfxl1 |
CC |
CCGGGGAC |
5: 72,716,464 (GRCm39) |
|
probably benign |
Het |
| Noc2l |
CTG |
CTGTTG |
4: 156,324,552 (GRCm39) |
|
probably benign |
Het |
| Noc2l |
GGTAG |
GG |
4: 156,325,958 (GRCm39) |
|
probably benign |
Homo |
| Noc2l |
GCT |
GCTTCT |
4: 156,324,551 (GRCm39) |
|
probably benign |
Het |
| Nxpe5 |
C |
T |
5: 138,228,196 (GRCm39) |
|
probably benign |
Het |
| Or10j2 |
GGGCTGCTTGTGGCAAT |
G |
1: 173,098,197 (GRCm39) |
|
probably null |
Het |
| Or51a43 |
G |
C |
7: 103,720,499 (GRCm39) |
|
probably benign |
Homo |
| Or51f2 |
CT |
CTAATTGCCTT |
7: 102,526,440 (GRCm39) |
|
probably benign |
Homo |
| Or8b41 |
A |
G |
9: 38,054,484 (GRCm39) |
I13V |
probably benign |
Homo |
| Or8u3-ps |
CAG |
CAGAG |
2: 85,953,104 (GRCm39) |
|
probably null |
Homo |
| Osmr |
C |
CTCA |
15: 6,867,187 (GRCm39) |
|
probably null |
Homo |
| Patl2 |
GC |
GCTAC |
2: 121,956,625 (GRCm39) |
|
probably null |
Het |
| Patl2 |
C |
CTGA |
2: 121,956,626 (GRCm39) |
|
probably benign |
Het |
| Patl2 |
CTG |
CTGTTG |
2: 121,956,617 (GRCm39) |
|
probably benign |
Het |
| Pdik1l |
GTTTTTGTTTT |
GTTTTTGTTTTTTTTTTGTTTT |
4: 134,006,678 (GRCm39) |
|
probably null |
Homo |
| Pdik1l |
ACCACC |
ACCACCCCCACC |
4: 134,006,817 (GRCm39) |
|
probably benign |
Het |
| Phc1 |
GCTG |
GCTGCTTCTG |
6: 122,300,557 (GRCm39) |
|
probably benign |
Het |
| Piezo1 |
G |
A |
8: 123,222,308 (GRCm39) |
R503W |
probably damaging |
Homo |
| Pitrm1 |
TTTTA |
T |
13: 6,610,632 (GRCm39) |
|
probably benign |
Homo |
| Pkdrej |
TG |
TGGGAGCG |
15: 85,703,881 (GRCm39) |
|
probably benign |
Homo |
| Pla2g4e |
AGGG |
A |
2: 120,075,205 (GRCm39) |
|
probably benign |
Homo |
| Plekhs1 |
AC |
ACCTCCCCCGAGCC |
19: 56,468,295 (GRCm39) |
|
probably benign |
Het |
| Pnma8a |
CCTCATGATGCACCTGCTTCAACATC |
CCTCATGATGCACCTGCTTCAACATCTCATGATGCACCTGCTTCAACATC |
7: 16,695,350 (GRCm39) |
|
probably benign |
Homo |
| Pnma8b |
TGGA |
T |
7: 16,679,931 (GRCm39) |
|
probably benign |
Het |
| Ppp1r3f |
C |
A |
X: 7,426,575 (GRCm39) |
G562V |
probably damaging |
Homo |
| Prr13 |
CTC |
CTCATC |
15: 102,370,608 (GRCm39) |
|
probably benign |
Het |
| Prss41 |
CACA |
C |
17: 24,063,071 (GRCm39) |
|
probably benign |
Het |
| Prtg |
GTAAC |
G |
9: 72,764,363 (GRCm39) |
|
probably benign |
Het |
| Ptk2b |
C |
T |
14: 66,411,298 (GRCm39) |
R411Q |
possibly damaging |
Homo |
| Ptms |
TCT |
TCTGCT |
6: 124,891,420 (GRCm39) |
|
probably benign |
Homo |
| Ptms |
C |
CTTG |
6: 124,891,424 (GRCm39) |
|
probably benign |
Homo |
| Ptms |
TTC |
TTCGTC |
6: 124,891,422 (GRCm39) |
|
probably benign |
Homo |
| Ptpn23 |
G |
T |
9: 110,216,701 (GRCm39) |
P1052T |
probably benign |
Homo |
| Rab3il1 |
C |
A |
19: 10,011,115 (GRCm39) |
A264E |
probably damaging |
Homo |
| Rbm6 |
GCTGT |
G |
9: 107,659,954 (GRCm39) |
|
probably null |
Homo |
| Rtbdn |
TAG |
TAGGGGCAG |
8: 85,682,790 (GRCm39) |
|
probably benign |
Het |
| Rtbdn |
GGC |
GGCAGCTGC |
8: 85,682,806 (GRCm39) |
|
probably benign |
Het |
| Rtbdn |
CGGC |
CGGCAGGGGC |
8: 85,682,805 (GRCm39) |
|
probably benign |
Het |
| Rtbdn |
AGCG |
AGCGTCCGCG |
8: 85,682,797 (GRCm39) |
|
probably benign |
Het |
| Sbp |
CAAAG |
CAAAGCTGCTGACAAAAAAG |
17: 24,164,356 (GRCm39) |
|
probably benign |
Het |
| Sbp |
G |
GCTGACAACAAAGATC |
17: 24,164,363 (GRCm39) |
|
probably benign |
Het |
| Setd1a |
GTGGTAGTG |
GTGGTAGTGTTGGTAGTG |
7: 127,384,484 (GRCm39) |
|
probably benign |
Het |
| Sfswap |
GCCCACTC |
GCCCACTCATCCCACTC |
5: 129,646,820 (GRCm39) |
|
probably benign |
Het |
| Six3 |
GGC |
GGCAGC |
17: 85,928,785 (GRCm39) |
|
probably benign |
Het |
| Six3 |
GCG |
GCGCCG |
17: 85,928,786 (GRCm39) |
|
probably benign |
Het |
| Six3 |
CGG |
CGGGGG |
17: 85,928,790 (GRCm39) |
|
probably benign |
Het |
| Six3 |
GGC |
GGCAGC |
17: 85,928,791 (GRCm39) |
|
probably benign |
Het |
| Six3 |
CGG |
CGGGGG |
17: 85,928,793 (GRCm39) |
|
probably benign |
Het |
| Six3 |
CGG |
CGGGGG |
17: 85,928,796 (GRCm39) |
|
probably benign |
Het |
| Slc12a1 |
ACC |
ACCTTTGGCCACAACTCC |
2: 124,996,134 (GRCm39) |
|
probably benign |
Homo |
| Smarca2 |
CAGCAGCAGCAGCAGCAGCA |
CAGCAGCAGCAGCAGCAGCAGCAGCA |
19: 26,608,399 (GRCm39) |
|
probably benign |
Homo |
| Spaca1 |
TCGCTC |
TCGCTCGCGCTC |
4: 34,049,836 (GRCm39) |
|
probably benign |
Het |
| Spag1 |
TTC |
TTCGTC |
15: 36,197,879 (GRCm39) |
|
probably benign |
Het |
| Spag17 |
AGG |
AGGCGG |
3: 99,963,573 (GRCm39) |
|
probably benign |
Het |
| Spata31h1 |
TTCA |
T |
10: 82,121,303 (GRCm39) |
|
probably benign |
Homo |
| Srebf2 |
G |
T |
15: 82,069,536 (GRCm39) |
A693S |
probably damaging |
Homo |
| Srpk2 |
T |
C |
5: 23,750,194 (GRCm39) |
|
probably null |
Homo |
| Sry |
AACTGCT |
A |
Y: 2,663,195 (GRCm39) |
|
probably benign |
Het |
| Sry |
GTG |
GTGTTG |
Y: 2,662,837 (GRCm39) |
|
probably benign |
Homo |
| Sry |
TGG |
TGGGGG |
Y: 2,662,838 (GRCm39) |
|
probably benign |
Homo |
| Supt20 |
CAGCAG |
CAGCAGGAGCAG |
3: 54,635,079 (GRCm39) |
|
probably benign |
Het |
| Supt20 |
CAGCAG |
CAGCAGAAGCAG |
3: 54,635,082 (GRCm39) |
|
probably benign |
Het |
| Supt20 |
GCAGCA |
GCAGCAACAGCA |
3: 54,635,078 (GRCm39) |
|
probably benign |
Het |
| Tcof1 |
GGGTA |
G |
18: 60,961,722 (GRCm39) |
|
probably benign |
Homo |
| Tdpoz3 |
A |
C |
3: 93,733,981 (GRCm39) |
N219H |
probably benign |
Het |
| Tesk1 |
C |
CCCCG |
4: 43,447,004 (GRCm39) |
|
probably null |
Homo |
| Tob1 |
GCA |
GCAACA |
11: 94,105,290 (GRCm39) |
|
probably benign |
Het |
| Tob1 |
CACA |
CACAACA |
11: 94,105,277 (GRCm39) |
|
probably benign |
Het |
| Tob1 |
A |
AGCC |
11: 94,105,304 (GRCm39) |
|
probably benign |
Het |
| Trav15-2-dv6-2 |
AG |
AGAGG |
14: 53,887,213 (GRCm39) |
|
probably benign |
Homo |
| Trav15-2-dv6-2 |
G |
GAAA |
14: 53,887,214 (GRCm39) |
|
probably benign |
Homo |
| Trim63 |
GAGT |
G |
4: 134,055,036 (GRCm39) |
|
probably benign |
Het |
| Tsbp1 |
CAG |
CAGAAG |
17: 34,679,025 (GRCm39) |
|
probably benign |
Het |
| Tsbp1 |
GCA |
GCATCA |
17: 34,679,042 (GRCm39) |
|
probably benign |
Het |
| Tsen2 |
G |
GAGA |
6: 115,537,038 (GRCm39) |
|
probably benign |
Het |
| Ttf2 |
TC |
TCCCC |
3: 100,870,476 (GRCm39) |
|
probably benign |
Homo |
| Tusc1 |
ACCGCC |
ACCGCCCCCGCC |
4: 93,223,550 (GRCm39) |
|
probably benign |
Homo |
| Ubqlnl |
TGAG |
T |
7: 103,799,042 (GRCm39) |
|
probably benign |
Homo |
| Ubtf |
CCT |
CCTACT |
11: 102,197,774 (GRCm39) |
|
probably null |
Het |
| Ubtf |
TCC |
TCCACC |
11: 102,197,776 (GRCm39) |
|
probably benign |
Het |
| Vps13b |
G |
T |
15: 35,847,103 (GRCm39) |
A2629S |
probably damaging |
Homo |
| Wasf3 |
G |
T |
5: 146,407,060 (GRCm39) |
R460L |
probably damaging |
Het |
| Zc3h13 |
TGCGAGATG |
TGCGAGATGAGCGAGATG |
14: 75,561,039 (GRCm39) |
|
probably benign |
Homo |
| Zc3h13 |
ATGTGCGAG |
ATGTGCGAGGTGTGCGAG |
14: 75,561,036 (GRCm39) |
|
probably benign |
Homo |
| Zfhx3 |
GCAACA |
GCAACAACAACAACA |
8: 109,682,720 (GRCm39) |
|
probably benign |
Het |
| Zfhx3 |
GCA |
GCAACAGCACCA |
8: 109,682,735 (GRCm39) |
|
probably benign |
Het |
| Zfhx3 |
AGCA |
AGCAACAGACGCA |
8: 109,682,734 (GRCm39) |
|
probably benign |
Het |
| Zfp111 |
TCA |
TCAACA |
7: 23,899,230 (GRCm39) |
|
probably benign |
Homo |
| Zfp112 |
CATGA |
CATGATGA |
7: 23,824,832 (GRCm39) |
|
probably benign |
Homo |
| Zfp26 |
C |
A |
9: 20,349,842 (GRCm39) |
A241S |
probably benign |
Homo |
| Zfp282 |
CGG |
CGGGGG |
6: 47,881,724 (GRCm39) |
|
probably benign |
Het |
| Zfp282 |
CGG |
CGGGGG |
6: 47,881,733 (GRCm39) |
|
probably benign |
Het |
| Zfp335 |
TC |
TCCCC |
2: 164,749,404 (GRCm39) |
|
probably benign |
Het |
| Zfp335 |
TCC |
TCCGCC |
2: 164,749,395 (GRCm39) |
|
probably benign |
Het |
| Zfp335 |
CTC |
CTCGTC |
2: 164,749,394 (GRCm39) |
|
probably benign |
Het |
| Zfp462 |
CCACC |
CCACCTCAGCCACAGTCACC |
4: 55,009,758 (GRCm39) |
|
probably benign |
Het |
| Zfp462 |
ACC |
ACCTCAGCCACAGTCGCC |
4: 55,009,760 (GRCm39) |
|
probably benign |
Het |
| Zfp598 |
ACCACC |
ACCACCCCCACC |
17: 24,899,750 (GRCm39) |
|
probably benign |
Het |
| Zfp598 |
AC |
ACCACCGC |
17: 24,899,765 (GRCm39) |
|
probably benign |
Het |
| Zfp598 |
ACCACC |
ACCACCGCCACC |
17: 24,899,756 (GRCm39) |
|
probably benign |
Het |
| Zfp831 |
TCC |
TCCCCC |
2: 174,487,264 (GRCm39) |
|
probably benign |
Het |
| Zfp831 |
TC |
TCCGC |
2: 174,487,276 (GRCm39) |
|
probably benign |
Het |
| Zfp831 |
CTC |
CTCATC |
2: 174,487,269 (GRCm39) |
|
probably benign |
Het |
| Zfp93 |
CAGGCATAG |
CAG |
7: 23,974,814 (GRCm39) |
|
probably benign |
Homo |
| Zscan10 |
TGACG |
TG |
17: 23,828,419 (GRCm39) |
|
probably benign |
Homo |
|
| Other mutations in Stard9 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01103:Stard9
|
APN |
2 |
120,532,328 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
IGL01122:Stard9
|
APN |
2 |
120,528,960 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL01318:Stard9
|
APN |
2 |
120,529,200 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
IGL01371:Stard9
|
APN |
2 |
120,531,849 (GRCm39) |
missense |
probably benign |
0.04 |
|
IGL01394:Stard9
|
APN |
2 |
120,536,808 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
IGL01531:Stard9
|
APN |
2 |
120,504,085 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL01721:Stard9
|
APN |
2 |
120,533,811 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01810:Stard9
|
APN |
2 |
120,529,565 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL01829:Stard9
|
APN |
2 |
120,536,927 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
IGL01916:Stard9
|
APN |
2 |
120,498,497 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02031:Stard9
|
APN |
2 |
120,532,820 (GRCm39) |
missense |
probably benign |
0.27 |
|
IGL02081:Stard9
|
APN |
2 |
120,495,391 (GRCm39) |
missense |
probably damaging |
0.98 |
|
IGL02558:Stard9
|
APN |
2 |
120,527,388 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
IGL02646:Stard9
|
APN |
2 |
120,529,473 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02873:Stard9
|
APN |
2 |
120,544,288 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03195:Stard9
|
APN |
2 |
120,536,283 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03204:Stard9
|
APN |
2 |
120,536,283 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03014:Stard9
|
UTSW |
2 |
120,532,675 (GRCm39) |
unclassified |
probably benign |
|
|
PIT4151001:Stard9
|
UTSW |
2 |
120,533,237 (GRCm39) |
nonsense |
probably null |
|
|
PIT4498001:Stard9
|
UTSW |
2 |
120,527,916 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R0027:Stard9
|
UTSW |
2 |
120,533,982 (GRCm39) |
missense |
probably benign |
|
|
R0027:Stard9
|
UTSW |
2 |
120,533,982 (GRCm39) |
missense |
probably benign |
|
|
R0038:Stard9
|
UTSW |
2 |
120,526,313 (GRCm39) |
missense |
probably benign |
|
|
R0049:Stard9
|
UTSW |
2 |
120,530,300 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0049:Stard9
|
UTSW |
2 |
120,530,300 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0116:Stard9
|
UTSW |
2 |
120,464,736 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0398:Stard9
|
UTSW |
2 |
120,526,788 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0479:Stard9
|
UTSW |
2 |
120,528,077 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0556:Stard9
|
UTSW |
2 |
120,529,404 (GRCm39) |
missense |
probably benign |
0.09 |
|
R0589:Stard9
|
UTSW |
2 |
120,529,028 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0609:Stard9
|
UTSW |
2 |
120,536,787 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0611:Stard9
|
UTSW |
2 |
120,529,738 (GRCm39) |
missense |
probably benign |
0.00 |
|
R0683:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0751:Stard9
|
UTSW |
2 |
120,527,966 (GRCm39) |
missense |
probably benign |
0.04 |
|
R0833:Stard9
|
UTSW |
2 |
120,527,480 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R0836:Stard9
|
UTSW |
2 |
120,527,480 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R0838:Stard9
|
UTSW |
2 |
120,531,323 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0848:Stard9
|
UTSW |
2 |
120,526,304 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0849:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0961:Stard9
|
UTSW |
2 |
120,523,920 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0993:Stard9
|
UTSW |
2 |
120,535,650 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1005:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1006:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1115:Stard9
|
UTSW |
2 |
120,523,331 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1163:Stard9
|
UTSW |
2 |
120,526,694 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R1199:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1200:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1331:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1332:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1333:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1334:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1335:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1336:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1338:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1346:Stard9
|
UTSW |
2 |
120,543,929 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1370:Stard9
|
UTSW |
2 |
120,527,958 (GRCm39) |
missense |
probably benign |
0.11 |
|
R1384:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1401:Stard9
|
UTSW |
2 |
120,543,328 (GRCm39) |
splice site |
probably benign |
|
|
R1416:Stard9
|
UTSW |
2 |
120,531,453 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1453:Stard9
|
UTSW |
2 |
120,496,857 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1468:Stard9
|
UTSW |
2 |
120,533,678 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R1468:Stard9
|
UTSW |
2 |
120,533,678 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R1525:Stard9
|
UTSW |
2 |
120,532,533 (GRCm39) |
missense |
probably benign |
0.09 |
|
R1538:Stard9
|
UTSW |
2 |
120,527,192 (GRCm39) |
missense |
probably benign |
0.25 |
|
R1614:Stard9
|
UTSW |
2 |
120,528,156 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1654:Stard9
|
UTSW |
2 |
120,534,203 (GRCm39) |
missense |
probably benign |
0.37 |
|
R1658:Stard9
|
UTSW |
2 |
120,532,023 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1686:Stard9
|
UTSW |
2 |
120,529,973 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1797:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1803:Stard9
|
UTSW |
2 |
120,531,970 (GRCm39) |
missense |
probably benign |
0.24 |
|
R1806:Stard9
|
UTSW |
2 |
120,509,934 (GRCm39) |
splice site |
probably null |
|
|
R1847:Stard9
|
UTSW |
2 |
120,528,970 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R1853:Stard9
|
UTSW |
2 |
120,519,232 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1892:Stard9
|
UTSW |
2 |
120,524,189 (GRCm39) |
missense |
probably benign |
0.01 |
|
R1906:Stard9
|
UTSW |
2 |
120,526,908 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1907:Stard9
|
UTSW |
2 |
120,544,293 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1930:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1933:Stard9
|
UTSW |
2 |
120,529,137 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R1989:Stard9
|
UTSW |
2 |
120,531,887 (GRCm39) |
missense |
probably benign |
|
|
R1999:Stard9
|
UTSW |
2 |
120,523,349 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2004:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2005:Stard9
|
UTSW |
2 |
120,504,117 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2005:Stard9
|
UTSW |
2 |
120,495,426 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R2021:Stard9
|
UTSW |
2 |
120,534,716 (GRCm39) |
missense |
probably benign |
0.05 |
|
R2025:Stard9
|
UTSW |
2 |
120,532,879 (GRCm39) |
missense |
probably benign |
0.20 |
|
R2190:Stard9
|
UTSW |
2 |
120,544,601 (GRCm39) |
missense |
probably benign |
0.22 |
|
R2204:Stard9
|
UTSW |
2 |
120,529,012 (GRCm39) |
frame shift |
probably null |
|
|
R2422:Stard9
|
UTSW |
2 |
120,530,765 (GRCm39) |
missense |
probably benign |
0.29 |
|
R3401:Stard9
|
UTSW |
2 |
120,534,170 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R3618:Stard9
|
UTSW |
2 |
120,529,500 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R3619:Stard9
|
UTSW |
2 |
120,529,500 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R3900:Stard9
|
UTSW |
2 |
120,544,030 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R3943:Stard9
|
UTSW |
2 |
120,528,710 (GRCm39) |
missense |
probably benign |
0.11 |
|
R4022:Stard9
|
UTSW |
2 |
120,534,636 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4223:Stard9
|
UTSW |
2 |
120,495,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4224:Stard9
|
UTSW |
2 |
120,495,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4225:Stard9
|
UTSW |
2 |
120,495,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4345:Stard9
|
UTSW |
2 |
120,532,427 (GRCm39) |
missense |
probably benign |
0.43 |
|
R4382:Stard9
|
UTSW |
2 |
120,464,703 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4453:Stard9
|
UTSW |
2 |
120,528,272 (GRCm39) |
missense |
probably benign |
|
|
R4499:Stard9
|
UTSW |
2 |
120,530,722 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4524:Stard9
|
UTSW |
2 |
120,526,926 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4671:Stard9
|
UTSW |
2 |
120,529,121 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4701:Stard9
|
UTSW |
2 |
120,536,194 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R4744:Stard9
|
UTSW |
2 |
120,526,604 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4822:Stard9
|
UTSW |
2 |
120,526,422 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R4847:Stard9
|
UTSW |
2 |
120,533,594 (GRCm39) |
missense |
probably benign |
0.18 |
|
R4863:Stard9
|
UTSW |
2 |
120,531,341 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4898:Stard9
|
UTSW |
2 |
120,536,900 (GRCm39) |
nonsense |
probably null |
|
|
R5033:Stard9
|
UTSW |
2 |
120,523,880 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5087:Stard9
|
UTSW |
2 |
120,527,500 (GRCm39) |
nonsense |
probably null |
|
|
R5157:Stard9
|
UTSW |
2 |
120,528,342 (GRCm39) |
missense |
probably benign |
|
|
R5213:Stard9
|
UTSW |
2 |
120,529,707 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5237:Stard9
|
UTSW |
2 |
120,529,839 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R5257:Stard9
|
UTSW |
2 |
120,529,824 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5258:Stard9
|
UTSW |
2 |
120,529,824 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5273:Stard9
|
UTSW |
2 |
120,535,568 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R5286:Stard9
|
UTSW |
2 |
120,532,428 (GRCm39) |
missense |
probably benign |
0.43 |
|
R5288:Stard9
|
UTSW |
2 |
120,531,111 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5292:Stard9
|
UTSW |
2 |
120,529,626 (GRCm39) |
missense |
probably benign |
0.17 |
|
R5328:Stard9
|
UTSW |
2 |
120,529,711 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5385:Stard9
|
UTSW |
2 |
120,531,111 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5386:Stard9
|
UTSW |
2 |
120,531,111 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R5393:Stard9
|
UTSW |
2 |
120,533,387 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R5405:Stard9
|
UTSW |
2 |
120,524,149 (GRCm39) |
missense |
probably benign |
0.17 |
|
R5685:Stard9
|
UTSW |
2 |
120,535,803 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5749:Stard9
|
UTSW |
2 |
120,534,267 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5780:Stard9
|
UTSW |
2 |
120,533,877 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5901:Stard9
|
UTSW |
2 |
120,531,851 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5941:Stard9
|
UTSW |
2 |
120,544,039 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5960:Stard9
|
UTSW |
2 |
120,530,442 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5966:Stard9
|
UTSW |
2 |
120,527,580 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5967:Stard9
|
UTSW |
2 |
120,537,375 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6012:Stard9
|
UTSW |
2 |
120,535,067 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6019:Stard9
|
UTSW |
2 |
120,524,196 (GRCm39) |
frame shift |
probably null |
|
|
R6020:Stard9
|
UTSW |
2 |
120,524,196 (GRCm39) |
frame shift |
probably null |
|
|
R6036:Stard9
|
UTSW |
2 |
120,530,556 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6036:Stard9
|
UTSW |
2 |
120,530,556 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6090:Stard9
|
UTSW |
2 |
120,524,135 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6192:Stard9
|
UTSW |
2 |
120,527,241 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6228:Stard9
|
UTSW |
2 |
120,544,231 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6235:Stard9
|
UTSW |
2 |
120,544,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6280:Stard9
|
UTSW |
2 |
120,531,608 (GRCm39) |
missense |
probably benign |
|
|
R6338:Stard9
|
UTSW |
2 |
120,527,966 (GRCm39) |
missense |
probably benign |
|
|
R6344:Stard9
|
UTSW |
2 |
120,534,801 (GRCm39) |
missense |
probably benign |
0.12 |
|
R6364:Stard9
|
UTSW |
2 |
120,543,910 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6383:Stard9
|
UTSW |
2 |
120,496,888 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6644:Stard9
|
UTSW |
2 |
120,526,253 (GRCm39) |
missense |
probably benign |
0.11 |
|
R6747:Stard9
|
UTSW |
2 |
120,528,864 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R6833:Stard9
|
UTSW |
2 |
120,531,740 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6836:Stard9
|
UTSW |
2 |
120,530,324 (GRCm39) |
missense |
probably benign |
0.15 |
|
R6861:Stard9
|
UTSW |
2 |
120,535,667 (GRCm39) |
missense |
probably benign |
0.09 |
|
R6872:Stard9
|
UTSW |
2 |
120,544,549 (GRCm39) |
nonsense |
probably null |
|
|
R6875:Stard9
|
UTSW |
2 |
120,527,917 (GRCm39) |
missense |
probably benign |
0.04 |
|
R6915:Stard9
|
UTSW |
2 |
120,533,111 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6934:Stard9
|
UTSW |
2 |
120,528,176 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6943:Stard9
|
UTSW |
2 |
120,532,677 (GRCm39) |
missense |
probably benign |
0.29 |
|
R7009:Stard9
|
UTSW |
2 |
120,527,672 (GRCm39) |
missense |
probably benign |
0.37 |
|
R7031:Stard9
|
UTSW |
2 |
120,530,931 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R7132:Stard9
|
UTSW |
2 |
120,509,859 (GRCm39) |
nonsense |
probably null |
|
|
R7151:Stard9
|
UTSW |
2 |
120,526,623 (GRCm39) |
missense |
probably benign |
|
|
R7154:Stard9
|
UTSW |
2 |
120,535,023 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7154:Stard9
|
UTSW |
2 |
120,531,795 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7165:Stard9
|
UTSW |
2 |
120,534,639 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7260:Stard9
|
UTSW |
2 |
120,537,419 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7270:Stard9
|
UTSW |
2 |
120,464,755 (GRCm39) |
nonsense |
probably null |
|
|
R7282:Stard9
|
UTSW |
2 |
120,528,984 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7344:Stard9
|
UTSW |
2 |
120,535,167 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R7347:Stard9
|
UTSW |
2 |
120,497,015 (GRCm39) |
missense |
probably benign |
|
|
R7359:Stard9
|
UTSW |
2 |
120,528,761 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7375:Stard9
|
UTSW |
2 |
120,495,483 (GRCm39) |
splice site |
probably null |
|
|
R7410:Stard9
|
UTSW |
2 |
120,531,978 (GRCm39) |
missense |
probably benign |
0.41 |
|
R7422:Stard9
|
UTSW |
2 |
120,532,633 (GRCm39) |
missense |
probably benign |
0.21 |
|
R7475:Stard9
|
UTSW |
2 |
120,518,591 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7523:Stard9
|
UTSW |
2 |
120,530,078 (GRCm39) |
missense |
probably benign |
|
|
R7553:Stard9
|
UTSW |
2 |
120,524,289 (GRCm39) |
splice site |
probably null |
|
|
R7624:Stard9
|
UTSW |
2 |
120,518,627 (GRCm39) |
missense |
probably benign |
0.15 |
|
R7761:Stard9
|
UTSW |
2 |
120,529,860 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7794:Stard9
|
UTSW |
2 |
120,534,911 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7819:Stard9
|
UTSW |
2 |
120,531,465 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7823:Stard9
|
UTSW |
2 |
120,532,587 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7837:Stard9
|
UTSW |
2 |
120,534,146 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7889:Stard9
|
UTSW |
2 |
120,534,942 (GRCm39) |
missense |
probably benign |
0.11 |
|
R7905:Stard9
|
UTSW |
2 |
120,526,562 (GRCm39) |
missense |
not run |
|
|
R7956:Stard9
|
UTSW |
2 |
120,535,852 (GRCm39) |
nonsense |
probably null |
|
|
R8013:Stard9
|
UTSW |
2 |
120,518,582 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8113:Stard9
|
UTSW |
2 |
120,534,911 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8114:Stard9
|
UTSW |
2 |
120,534,911 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8116:Stard9
|
UTSW |
2 |
120,495,420 (GRCm39) |
nonsense |
probably null |
|
|
R8117:Stard9
|
UTSW |
2 |
120,534,911 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8118:Stard9
|
UTSW |
2 |
120,534,911 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8170:Stard9
|
UTSW |
2 |
120,530,529 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R8300:Stard9
|
UTSW |
2 |
120,535,250 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R8333:Stard9
|
UTSW |
2 |
120,532,270 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8337:Stard9
|
UTSW |
2 |
120,510,306 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8536:Stard9
|
UTSW |
2 |
120,545,140 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R8682:Stard9
|
UTSW |
2 |
120,533,796 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R8696:Stard9
|
UTSW |
2 |
120,531,595 (GRCm39) |
missense |
probably benign |
0.02 |
|
R8708:Stard9
|
UTSW |
2 |
120,534,059 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8732:Stard9
|
UTSW |
2 |
120,510,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8798:Stard9
|
UTSW |
2 |
120,535,212 (GRCm39) |
missense |
probably benign |
0.09 |
|
R8807:Stard9
|
UTSW |
2 |
120,535,932 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8807:Stard9
|
UTSW |
2 |
120,535,943 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8862:Stard9
|
UTSW |
2 |
120,534,099 (GRCm39) |
missense |
probably benign |
|
|
R8920:Stard9
|
UTSW |
2 |
120,533,088 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9026:Stard9
|
UTSW |
2 |
120,536,283 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9048:Stard9
|
UTSW |
2 |
120,508,415 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9049:Stard9
|
UTSW |
2 |
120,510,418 (GRCm39) |
missense |
probably benign |
0.30 |
|
R9152:Stard9
|
UTSW |
2 |
120,529,068 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9189:Stard9
|
UTSW |
2 |
120,533,500 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R9238:Stard9
|
UTSW |
2 |
120,528,447 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9372:Stard9
|
UTSW |
2 |
120,495,420 (GRCm39) |
nonsense |
probably null |
|
|
R9393:Stard9
|
UTSW |
2 |
120,518,656 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R9444:Stard9
|
UTSW |
2 |
120,495,414 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9514:Stard9
|
UTSW |
2 |
120,534,564 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9515:Stard9
|
UTSW |
2 |
120,534,564 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9516:Stard9
|
UTSW |
2 |
120,534,564 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9570:Stard9
|
UTSW |
2 |
120,534,714 (GRCm39) |
missense |
probably benign |
0.02 |
|
R9649:Stard9
|
UTSW |
2 |
120,526,635 (GRCm39) |
missense |
probably benign |
0.20 |
|
R9789:Stard9
|
UTSW |
2 |
120,510,417 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0023:Stard9
|
UTSW |
2 |
120,533,444 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
X0023:Stard9
|
UTSW |
2 |
120,533,225 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1176:Stard9
|
UTSW |
2 |
120,528,803 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Stard9
|
UTSW |
2 |
120,527,093 (GRCm39) |
missense |
probably benign |
|
|
Z1176:Stard9
|
UTSW |
2 |
120,526,299 (GRCm39) |
missense |
probably benign |
0.01 |
|
Z1177:Stard9
|
UTSW |
2 |
120,504,157 (GRCm39) |
critical splice donor site |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- AACAGCTTCCATTCATCTCGG -3'
(R):5'- TTTGATGCCCTGCTTGAAGG -3'
Sequencing Primer
(F):5'- CCATTCATCTCGGTGGAGGAAG -3'
(R):5'- ATGCCCTGCTTGAAGGAGATG -3'
|
| Posted On |
2018-04-05 |
Incidental Mutation