Incidental Mutation 'R4998:Baz1a'
| ID |
389668 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Baz1a
|
| Ensembl Gene |
ENSMUSG00000035021 |
| Gene Name |
bromodomain adjacent to zinc finger domain 1A |
| Synonyms |
Gtl5, Wcrf180, Acf1 |
| MMRRC Submission |
042592-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4998 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
12 |
| Chromosomal Location |
54939774-55061133 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 55021922 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Glycine
at position 120
(E120G)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000133478
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000038926]
[ENSMUST00000172875]
[ENSMUST00000173177]
[ENSMUST00000173433]
[ENSMUST00000173529]
|
| AlphaFold |
O88379 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000038926
AA Change: E120G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000039757
Gene: ENSMUSG00000035021
AA Change: E120G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:WAC_Acf1_DNA_bd
|
23 |
122 |
4.4e-36 |
PFAM |
|
low complexity region
|
164 |
175 |
N/A |
INTRINSIC |
|
coiled coil region
|
312 |
397 |
N/A |
INTRINSIC |
|
Pfam:DDT
|
423 |
485 |
2.3e-14 |
PFAM |
|
low complexity region
|
519 |
530 |
N/A |
INTRINSIC |
|
Pfam:WHIM1
|
593 |
641 |
1.5e-8 |
PFAM |
|
low complexity region
|
658 |
696 |
N/A |
INTRINSIC |
|
low complexity region
|
725 |
738 |
N/A |
INTRINSIC |
|
low complexity region
|
774 |
796 |
N/A |
INTRINSIC |
|
low complexity region
|
861 |
873 |
N/A |
INTRINSIC |
|
Pfam:WHIM3
|
894 |
932 |
2e-16 |
PFAM |
|
low complexity region
|
1058 |
1073 |
N/A |
INTRINSIC |
|
PHD
|
1151 |
1197 |
9.46e-15 |
SMART |
|
RING
|
1152 |
1196 |
6.88e-1 |
SMART |
|
low complexity region
|
1214 |
1257 |
N/A |
INTRINSIC |
|
BROMO
|
1426 |
1534 |
2.18e-31 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000172875
AA Change: E120G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000134384
Gene: ENSMUSG00000035021
AA Change: E120G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:WAC_Acf1_DNA_bd
|
22 |
122 |
3e-39 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173177
|
| SMART Domains |
Protein: ENSMUSP00000133796
Gene: ENSMUSG00000035021
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:WAC_Acf1_DNA_bd
|
22 |
86 |
5.2e-27 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000173433
AA Change: E120G
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000133478
Gene: ENSMUSG00000035021
AA Change: E120G
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:WAC_Acf1_DNA_bd
|
22 |
122 |
1.1e-37 |
PFAM |
|
low complexity region
|
164 |
175 |
N/A |
INTRINSIC |
|
coiled coil region
|
312 |
397 |
N/A |
INTRINSIC |
|
DDT
|
422 |
487 |
1.54e-19 |
SMART |
|
low complexity region
|
518 |
529 |
N/A |
INTRINSIC |
|
Pfam:WHIM1
|
592 |
640 |
1.8e-8 |
PFAM |
|
low complexity region
|
657 |
695 |
N/A |
INTRINSIC |
|
low complexity region
|
722 |
735 |
N/A |
INTRINSIC |
|
low complexity region
|
771 |
793 |
N/A |
INTRINSIC |
|
low complexity region
|
858 |
870 |
N/A |
INTRINSIC |
|
low complexity region
|
1055 |
1070 |
N/A |
INTRINSIC |
|
PHD
|
1148 |
1194 |
9.46e-15 |
SMART |
|
RING
|
1149 |
1193 |
6.88e-1 |
SMART |
|
low complexity region
|
1211 |
1254 |
N/A |
INTRINSIC |
|
BROMO
|
1423 |
1531 |
2.18e-31 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000173529
|
| SMART Domains |
Protein: ENSMUSP00000134445
Gene: ENSMUSG00000035021
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:WAC_Acf1_DNA_bd
|
22 |
82 |
7.5e-26 |
PFAM |
|
| Meta Mutation Damage Score |
0.9592 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.6%
- 20x: 93.3%
|
| Validation Efficiency |
97% (91/94) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The BAZ1A gene encodes the accessory subunit of the ATP-dependent chromatin assembly factor (ACF), a member of the ISWI ('imitation switch') family of chromatin remodeling complexes (summarized by Racki et al., 2009 [PubMed 20033039]).[supplied by OMIM, Apr 2010]
PHENOTYPE: Mice homozygous for a knock-out allele are viable and able to repair meiotic double-strand breaks but exhibit teratospermia, oligospermia, asthenospermia, and male infertility due to impaired spermiogenesis. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 86 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2310022A10Rik |
T |
C |
7: 27,271,088 (GRCm39) |
V135A |
probably damaging |
Het |
| Ankrd42 |
T |
C |
7: 92,273,282 (GRCm39) |
N115S |
possibly damaging |
Het |
| Calcrl |
A |
T |
2: 84,169,658 (GRCm39) |
V341E |
probably damaging |
Het |
| Card6 |
T |
C |
15: 5,129,564 (GRCm39) |
R611G |
probably benign |
Het |
| Cd70 |
A |
T |
17: 57,453,311 (GRCm39) |
S118T |
probably damaging |
Het |
| Chil5 |
T |
A |
3: 105,927,248 (GRCm39) |
I188F |
probably damaging |
Het |
| Clca4b |
C |
T |
3: 144,621,269 (GRCm39) |
V602I |
probably benign |
Het |
| Cldn10 |
G |
A |
14: 119,025,725 (GRCm39) |
G53S |
possibly damaging |
Het |
| Col6a4 |
A |
G |
9: 105,867,977 (GRCm39) |
|
probably benign |
Het |
| Cox8b |
T |
C |
7: 140,479,001 (GRCm39) |
E38G |
probably damaging |
Het |
| Cx3cl1 |
C |
G |
8: 95,507,053 (GRCm39) |
L353V |
probably damaging |
Het |
| Cyp2a4 |
G |
T |
7: 26,006,786 (GRCm39) |
Q48H |
probably damaging |
Het |
| Defb8 |
T |
C |
8: 19,497,603 (GRCm39) |
I3V |
probably benign |
Het |
| Dip2a |
A |
T |
10: 76,155,390 (GRCm39) |
L65* |
probably null |
Het |
| Dnaaf4 |
A |
G |
9: 72,867,960 (GRCm39) |
T74A |
possibly damaging |
Het |
| Dsg2 |
A |
T |
18: 20,734,578 (GRCm39) |
D852V |
probably benign |
Het |
| Edar |
T |
C |
10: 58,441,915 (GRCm39) |
R326G |
probably damaging |
Het |
| Egfr |
A |
G |
11: 16,831,493 (GRCm39) |
E554G |
possibly damaging |
Het |
| Eif2b3 |
A |
C |
4: 116,923,589 (GRCm39) |
K268T |
probably benign |
Het |
| Enox1 |
A |
T |
14: 77,738,875 (GRCm39) |
|
probably benign |
Het |
| Enpp3 |
C |
A |
10: 24,683,436 (GRCm39) |
M260I |
probably benign |
Het |
| Espn |
A |
T |
4: 152,220,040 (GRCm39) |
M361K |
possibly damaging |
Het |
| Fam107a |
T |
C |
14: 8,299,514 (GRCm38) |
N108S |
possibly damaging |
Het |
| Fbn2 |
A |
T |
18: 58,205,703 (GRCm39) |
V1125D |
probably damaging |
Het |
| Fbxo30 |
T |
A |
10: 11,166,507 (GRCm39) |
S410T |
probably damaging |
Het |
| Fchsd1 |
C |
T |
18: 38,092,926 (GRCm39) |
|
probably benign |
Het |
| Fcsk |
G |
A |
8: 111,614,435 (GRCm39) |
A618V |
probably damaging |
Het |
| Gm10715 |
T |
G |
9: 3,038,073 (GRCm39) |
|
probably benign |
Het |
| Gm10722 |
A |
C |
9: 3,001,041 (GRCm39) |
Y39S |
probably benign |
Het |
| Gm17416 |
C |
A |
2: 152,411,427 (GRCm39) |
P57Q |
probably damaging |
Het |
| Gm27013 |
A |
T |
6: 130,653,501 (GRCm39) |
C654S |
probably damaging |
Het |
| Gon4l |
G |
T |
3: 88,807,305 (GRCm39) |
E1666D |
probably damaging |
Het |
| Gypa |
T |
A |
8: 81,222,964 (GRCm39) |
S23T |
unknown |
Het |
| Gys1 |
C |
A |
7: 45,100,968 (GRCm39) |
|
probably benign |
Het |
| Hdac10 |
T |
A |
15: 89,008,143 (GRCm39) |
Q569L |
possibly damaging |
Het |
| Icos |
A |
G |
1: 61,032,941 (GRCm39) |
T47A |
possibly damaging |
Het |
| Igfn1 |
T |
A |
1: 135,882,404 (GRCm39) |
I2814F |
probably damaging |
Het |
| Kif27 |
A |
G |
13: 58,440,957 (GRCm39) |
S1153P |
probably damaging |
Het |
| Lin28a |
A |
C |
4: 133,746,028 (GRCm39) |
F9V |
possibly damaging |
Het |
| Lrriq3 |
T |
A |
3: 154,893,695 (GRCm39) |
N465K |
probably benign |
Het |
| Lsm14a |
T |
C |
7: 34,074,799 (GRCm39) |
E47G |
probably damaging |
Het |
| Mmel1 |
A |
G |
4: 154,969,967 (GRCm39) |
K177R |
probably benign |
Het |
| Ncstn |
T |
A |
1: 171,899,087 (GRCm39) |
N348I |
possibly damaging |
Het |
| Ninl |
A |
G |
2: 150,795,284 (GRCm39) |
I619T |
probably damaging |
Het |
| Npb |
T |
C |
11: 120,499,401 (GRCm39) |
Y23H |
probably damaging |
Het |
| Npepps |
A |
G |
11: 97,096,933 (GRCm39) |
|
probably benign |
Het |
| Or8k30 |
T |
C |
2: 86,339,699 (GRCm39) |
Y299H |
probably benign |
Het |
| Otop1 |
G |
A |
5: 38,451,892 (GRCm39) |
|
probably null |
Het |
| Pcdha1 |
T |
C |
18: 37,065,469 (GRCm39) |
L711P |
probably damaging |
Het |
| Pcyt1a |
A |
G |
16: 32,270,660 (GRCm39) |
|
probably benign |
Het |
| Pdpr |
G |
T |
8: 111,841,400 (GRCm39) |
V211F |
probably damaging |
Het |
| Pip4k2b |
T |
C |
11: 97,613,261 (GRCm39) |
N245S |
possibly damaging |
Het |
| Platr26 |
G |
A |
2: 71,561,214 (GRCm39) |
|
noncoding transcript |
Het |
| Plek |
A |
G |
11: 16,933,194 (GRCm39) |
|
probably null |
Het |
| Potefam3c |
G |
C |
8: 69,906,010 (GRCm39) |
N13K |
probably benign |
Het |
| Prdm15 |
A |
T |
16: 97,595,689 (GRCm39) |
D1046E |
probably damaging |
Het |
| Prr29 |
T |
G |
11: 106,267,779 (GRCm39) |
C175G |
probably benign |
Het |
| Ptpru |
A |
G |
4: 131,504,196 (GRCm39) |
V1097A |
probably damaging |
Het |
| Ramp2 |
T |
A |
11: 101,138,247 (GRCm39) |
|
probably benign |
Het |
| Rap1gap |
A |
G |
4: 137,455,595 (GRCm39) |
D381G |
possibly damaging |
Het |
| Rbbp6 |
T |
A |
7: 122,589,549 (GRCm39) |
D412E |
probably benign |
Het |
| Rgs4 |
C |
T |
1: 169,572,802 (GRCm39) |
V45I |
probably benign |
Het |
| Ryr2 |
C |
T |
13: 11,658,781 (GRCm39) |
R3614Q |
probably damaging |
Het |
| Shc3 |
G |
A |
13: 51,596,856 (GRCm39) |
|
probably null |
Het |
| Shmt2 |
A |
T |
10: 127,354,139 (GRCm39) |
C412S |
probably damaging |
Het |
| Slc25a45 |
A |
T |
19: 5,934,945 (GRCm39) |
N265Y |
probably damaging |
Het |
| Slc4a10 |
G |
C |
2: 62,074,783 (GRCm39) |
E316Q |
probably benign |
Het |
| Slc5a8 |
T |
C |
10: 88,743,919 (GRCm39) |
|
probably null |
Het |
| Snx31 |
A |
G |
15: 36,539,513 (GRCm39) |
V121A |
probably damaging |
Het |
| Socs3 |
T |
C |
11: 117,858,542 (GRCm39) |
E172G |
probably damaging |
Het |
| Tg |
A |
G |
15: 66,545,899 (GRCm39) |
D207G |
probably damaging |
Het |
| Them4 |
G |
T |
3: 94,237,088 (GRCm39) |
V183F |
probably damaging |
Het |
| Tkt |
G |
A |
14: 30,287,499 (GRCm39) |
W136* |
probably null |
Het |
| Tlcd3b |
C |
T |
7: 126,426,795 (GRCm39) |
R73C |
probably damaging |
Het |
| Tmc3 |
C |
A |
7: 83,271,529 (GRCm39) |
R894S |
probably benign |
Het |
| Tmem132a |
G |
T |
19: 10,836,305 (GRCm39) |
P742T |
probably benign |
Het |
| Tmem202 |
A |
G |
9: 59,432,129 (GRCm39) |
L66P |
probably damaging |
Het |
| Trbc1 |
G |
A |
6: 41,516,270 (GRCm39) |
|
probably benign |
Het |
| Trhr2 |
A |
G |
8: 123,085,511 (GRCm39) |
F158L |
probably benign |
Het |
| Ttc13 |
A |
T |
8: 125,406,795 (GRCm39) |
N595K |
probably damaging |
Het |
| Ucp1 |
A |
G |
8: 84,024,484 (GRCm39) |
|
probably null |
Het |
| Zbtb4 |
C |
T |
11: 69,669,497 (GRCm39) |
T740I |
probably benign |
Het |
| Zfp69 |
A |
T |
4: 120,804,522 (GRCm39) |
D116E |
possibly damaging |
Het |
| Zfp879 |
A |
G |
11: 50,728,796 (GRCm39) |
L66S |
probably damaging |
Het |
| Zfp955b |
T |
A |
17: 33,524,125 (GRCm39) |
|
probably benign |
Het |
| Zfyve1 |
T |
C |
12: 83,594,839 (GRCm39) |
I718V |
possibly damaging |
Het |
|
| Other mutations in Baz1a |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01108:Baz1a
|
APN |
12 |
54,963,516 (GRCm39) |
missense |
probably benign |
|
|
IGL01138:Baz1a
|
APN |
12 |
54,977,110 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01298:Baz1a
|
APN |
12 |
55,001,594 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02639:Baz1a
|
APN |
12 |
54,942,810 (GRCm39) |
splice site |
probably benign |
|
|
IGL02995:Baz1a
|
APN |
12 |
54,947,232 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03001:Baz1a
|
APN |
12 |
54,969,896 (GRCm39) |
missense |
possibly damaging |
0.50 |
|
IGL03104:Baz1a
|
APN |
12 |
54,941,743 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03135:Baz1a
|
APN |
12 |
54,976,375 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03151:Baz1a
|
APN |
12 |
54,955,934 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
IGL03235:Baz1a
|
APN |
12 |
54,945,320 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03240:Baz1a
|
APN |
12 |
54,974,352 (GRCm39) |
nonsense |
probably null |
|
|
Bezos
|
UTSW |
12 |
54,941,816 (GRCm39) |
nonsense |
probably null |
|
|
Flavia
|
UTSW |
12 |
55,022,093 (GRCm39) |
missense |
probably damaging |
1.00 |
|
gumdrops
|
UTSW |
12 |
54,947,233 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Kilter
|
UTSW |
12 |
54,947,317 (GRCm39) |
missense |
probably damaging |
0.99 |
|
Kisses
|
UTSW |
12 |
55,021,922 (GRCm39) |
missense |
probably damaging |
1.00 |
|
liverlips
|
UTSW |
12 |
54,967,928 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
smooch
|
UTSW |
12 |
54,963,608 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Smootch
|
UTSW |
12 |
54,958,170 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4458001:Baz1a
|
UTSW |
12 |
54,977,095 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0127:Baz1a
|
UTSW |
12 |
54,945,491 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R0183:Baz1a
|
UTSW |
12 |
54,958,172 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0393:Baz1a
|
UTSW |
12 |
54,965,221 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0532:Baz1a
|
UTSW |
12 |
54,981,605 (GRCm39) |
missense |
possibly damaging |
0.55 |
|
R0614:Baz1a
|
UTSW |
12 |
54,988,304 (GRCm39) |
nonsense |
probably null |
|
|
R0626:Baz1a
|
UTSW |
12 |
55,022,055 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0654:Baz1a
|
UTSW |
12 |
54,958,182 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0782:Baz1a
|
UTSW |
12 |
54,941,273 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0826:Baz1a
|
UTSW |
12 |
54,977,097 (GRCm39) |
nonsense |
probably null |
|
|
R0855:Baz1a
|
UTSW |
12 |
54,947,348 (GRCm39) |
splice site |
probably benign |
|
|
R0927:Baz1a
|
UTSW |
12 |
54,941,773 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0941:Baz1a
|
UTSW |
12 |
54,945,216 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1079:Baz1a
|
UTSW |
12 |
54,941,785 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R1157:Baz1a
|
UTSW |
12 |
54,976,349 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1647:Baz1a
|
UTSW |
12 |
55,021,983 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1731:Baz1a
|
UTSW |
12 |
54,965,330 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R1739:Baz1a
|
UTSW |
12 |
54,945,573 (GRCm39) |
nonsense |
probably null |
|
|
R1762:Baz1a
|
UTSW |
12 |
54,955,805 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1770:Baz1a
|
UTSW |
12 |
54,945,293 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1968:Baz1a
|
UTSW |
12 |
54,947,122 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R2037:Baz1a
|
UTSW |
12 |
54,976,431 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2111:Baz1a
|
UTSW |
12 |
54,958,170 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2215:Baz1a
|
UTSW |
12 |
55,022,154 (GRCm39) |
nonsense |
probably null |
|
|
R2282:Baz1a
|
UTSW |
12 |
54,963,597 (GRCm39) |
nonsense |
probably null |
|
|
R2875:Baz1a
|
UTSW |
12 |
54,969,904 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2890:Baz1a
|
UTSW |
12 |
54,945,302 (GRCm39) |
missense |
probably benign |
|
|
R2971:Baz1a
|
UTSW |
12 |
54,970,224 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3404:Baz1a
|
UTSW |
12 |
54,963,774 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3419:Baz1a
|
UTSW |
12 |
54,993,684 (GRCm39) |
missense |
probably benign |
0.05 |
|
R3699:Baz1a
|
UTSW |
12 |
54,963,831 (GRCm39) |
missense |
probably benign |
0.09 |
|
R3899:Baz1a
|
UTSW |
12 |
54,981,589 (GRCm39) |
missense |
probably benign |
0.01 |
|
R3927:Baz1a
|
UTSW |
12 |
54,967,928 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R4050:Baz1a
|
UTSW |
12 |
54,976,404 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4072:Baz1a
|
UTSW |
12 |
54,988,345 (GRCm39) |
missense |
probably benign |
0.18 |
|
R4196:Baz1a
|
UTSW |
12 |
54,958,200 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4289:Baz1a
|
UTSW |
12 |
54,947,233 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4455:Baz1a
|
UTSW |
12 |
54,958,153 (GRCm39) |
missense |
probably benign |
0.26 |
|
R4583:Baz1a
|
UTSW |
12 |
54,969,325 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4622:Baz1a
|
UTSW |
12 |
54,988,300 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4807:Baz1a
|
UTSW |
12 |
54,945,267 (GRCm39) |
missense |
probably benign |
0.28 |
|
R5239:Baz1a
|
UTSW |
12 |
54,945,129 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5379:Baz1a
|
UTSW |
12 |
54,941,133 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5408:Baz1a
|
UTSW |
12 |
54,969,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5678:Baz1a
|
UTSW |
12 |
54,947,317 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5810:Baz1a
|
UTSW |
12 |
54,974,500 (GRCm39) |
intron |
probably benign |
|
|
R6092:Baz1a
|
UTSW |
12 |
54,955,868 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R6317:Baz1a
|
UTSW |
12 |
55,001,585 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R6332:Baz1a
|
UTSW |
12 |
54,965,339 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6803:Baz1a
|
UTSW |
12 |
54,988,340 (GRCm39) |
missense |
probably null |
0.99 |
|
R7185:Baz1a
|
UTSW |
12 |
55,022,093 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7248:Baz1a
|
UTSW |
12 |
54,947,293 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7392:Baz1a
|
UTSW |
12 |
54,945,550 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8009:Baz1a
|
UTSW |
12 |
54,941,816 (GRCm39) |
nonsense |
probably null |
|
|
R8025:Baz1a
|
UTSW |
12 |
54,955,921 (GRCm39) |
missense |
probably benign |
0.34 |
|
R8392:Baz1a
|
UTSW |
12 |
54,969,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8862:Baz1a
|
UTSW |
12 |
55,032,624 (GRCm39) |
unclassified |
probably benign |
|
|
R8949:Baz1a
|
UTSW |
12 |
54,941,238 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9340:Baz1a
|
UTSW |
12 |
54,963,372 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9389:Baz1a
|
UTSW |
12 |
54,963,608 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9401:Baz1a
|
UTSW |
12 |
54,963,339 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9666:Baz1a
|
UTSW |
12 |
54,988,345 (GRCm39) |
missense |
probably benign |
0.18 |
|
R9722:Baz1a
|
UTSW |
12 |
54,946,882 (GRCm39) |
missense |
probably benign |
0.43 |
|
R9746:Baz1a
|
UTSW |
12 |
55,021,895 (GRCm39) |
frame shift |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- GGAAAGGTTTCATCACATCTCC -3'
(R):5'- ACGTATCAGGAAGCTCTTGAATC -3'
Sequencing Primer
(F):5'- AGACAGTCTTGCTCTATGGC -3'
(R):5'- TATCAGGAAGCTCTTGAATCCGAAAG -3'
|
| Posted On |
2016-06-06 |
Incidental Mutation