Incidental Mutation 'R7248:Btaf1'
| ID |
563724 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Btaf1
|
| Ensembl Gene |
ENSMUSG00000040565 |
| Gene Name |
B-TFIID TATA-box binding protein associated factor 1 |
| Synonyms |
E430027O22Rik |
| MMRRC Submission |
045311-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.967)
|
| Stock # |
R7248 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
19 |
| Chromosomal Location |
36903479-36990152 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 36922714 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamic Acid to Aspartic acid
at position 39
(E39D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000097093
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099494]
|
| AlphaFold |
E9QAE3 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000099494
AA Change: E39D
PolyPhen 2
Score 0.538 (Sensitivity: 0.88; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000097093
Gene: ENSMUSG00000040565
AA Change: E39D
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
87 |
98 |
N/A |
INTRINSIC |
|
low complexity region
|
143 |
152 |
N/A |
INTRINSIC |
|
PDB:3OC3|B
|
276 |
414 |
3e-6 |
PDB |
|
low complexity region
|
438 |
454 |
N/A |
INTRINSIC |
|
Pfam:DUF3535
|
585 |
1051 |
1.1e-133 |
PFAM |
|
low complexity region
|
1099 |
1110 |
N/A |
INTRINSIC |
|
low complexity region
|
1177 |
1192 |
N/A |
INTRINSIC |
|
DEXDc
|
1261 |
1469 |
3.02e-30 |
SMART |
|
low complexity region
|
1630 |
1641 |
N/A |
INTRINSIC |
|
HELICc
|
1657 |
1743 |
2.22e-19 |
SMART |
|
| Meta Mutation Damage Score |
0.0791 |
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.5%
- 20x: 98.4%
|
| Validation Efficiency |
97% (75/77) |
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a TAF (TATA box-binding protein-associated factor), which associates with TBP (TATA box-binding protein) to form the B-TFIID complex that is required for transcription initiation of genes by RNA polymerase II. This TAF has DNA-dependent ATPase activity, which drives the dissociation of TBP from DNA, freeing the TBP to associate with other TATA boxes or TATA-less promoters. [provided by RefSeq, Sep 2011]
PHENOTYPE: Embryos homozygous for a gene-trapped allele display growth retardation. Embryos homozygous for an ENU-induced allele show growth retardation, edema, abnormal blood circulation, myocardial trabeculae hypoplasia, and delayed head and brain development. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(40) : Gene trapped(40) |
| Other mutations in this stock |
Total: 76 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700006A11Rik |
A |
G |
3: 124,207,959 (GRCm39) |
|
probably null |
Het |
| Aldh16a1 |
A |
G |
7: 44,795,018 (GRCm39) |
Y484H |
probably damaging |
Het |
| Arhgap26 |
T |
C |
18: 39,439,907 (GRCm39) |
|
probably null |
Het |
| Atxn7l1 |
A |
G |
12: 33,417,194 (GRCm39) |
T452A |
probably benign |
Het |
| Baz1a |
C |
T |
12: 54,947,293 (GRCm39) |
E1119K |
probably damaging |
Het |
| Bud13 |
G |
T |
9: 46,194,413 (GRCm39) |
E29* |
probably null |
Het |
| Ccdc150 |
C |
T |
1: 54,344,057 (GRCm39) |
T530I |
probably benign |
Het |
| Chd6 |
G |
A |
2: 160,803,199 (GRCm39) |
Q2160* |
probably null |
Het |
| Cluap1 |
T |
A |
16: 3,737,364 (GRCm39) |
I172N |
possibly damaging |
Het |
| Cnot2 |
T |
C |
10: 116,334,278 (GRCm39) |
N329S |
probably benign |
Het |
| Cog4 |
A |
T |
8: 111,608,834 (GRCm39) |
T175S |
unknown |
Het |
| Coq7 |
C |
A |
7: 118,128,897 (GRCm39) |
R46L |
probably benign |
Het |
| D630045J12Rik |
A |
T |
6: 38,145,198 (GRCm39) |
V1276E |
probably damaging |
Het |
| Dcaf15 |
A |
G |
8: 84,829,394 (GRCm39) |
V116A |
possibly damaging |
Het |
| Ddr2 |
C |
T |
1: 169,822,198 (GRCm39) |
V417I |
probably benign |
Het |
| Defa25 |
G |
A |
8: 21,575,216 (GRCm39) |
C65Y |
probably damaging |
Het |
| Dhx38 |
T |
C |
8: 110,285,559 (GRCm39) |
T425A |
probably benign |
Het |
| Diaph1 |
T |
C |
18: 38,022,829 (GRCm39) |
T782A |
probably benign |
Het |
| Dnah7b |
T |
A |
1: 46,181,245 (GRCm39) |
M1044K |
possibly damaging |
Het |
| Dusp16 |
G |
A |
6: 134,695,940 (GRCm39) |
T297M |
probably benign |
Het |
| Esyt2 |
A |
G |
12: 116,305,858 (GRCm39) |
N363D |
probably damaging |
Het |
| Fasl |
C |
T |
1: 161,615,760 (GRCm39) |
C32Y |
possibly damaging |
Het |
| Flg |
T |
C |
3: 93,189,041 (GRCm39) |
V137A |
probably benign |
Het |
| Gm57858 |
T |
A |
3: 36,080,086 (GRCm39) |
T224S |
probably benign |
Het |
| Gpr150 |
G |
A |
13: 76,204,126 (GRCm39) |
A273V |
probably benign |
Het |
| Grk5 |
A |
G |
19: 60,879,045 (GRCm39) |
T10A |
probably benign |
Het |
| Hivep2 |
A |
G |
10: 14,006,909 (GRCm39) |
K1169R |
possibly damaging |
Het |
| Ido2 |
A |
C |
8: 25,030,657 (GRCm39) |
Y224* |
probably null |
Het |
| Ido2 |
A |
G |
8: 25,038,839 (GRCm39) |
I149T |
probably damaging |
Het |
| Iqca1l |
C |
T |
5: 24,749,269 (GRCm39) |
S743N |
probably benign |
Het |
| Kctd2 |
A |
G |
11: 115,312,845 (GRCm39) |
T126A |
possibly damaging |
Het |
| Khdc4 |
T |
C |
3: 88,600,886 (GRCm39) |
S228P |
probably damaging |
Het |
| Kif1a |
T |
C |
1: 92,969,305 (GRCm39) |
D1090G |
probably benign |
Het |
| Klrb1a |
A |
T |
6: 128,586,697 (GRCm39) |
H222Q |
possibly damaging |
Het |
| Kndc1 |
A |
C |
7: 139,500,699 (GRCm39) |
H688P |
probably damaging |
Het |
| Lrriq1 |
C |
A |
10: 103,059,611 (GRCm39) |
V141F |
possibly damaging |
Het |
| Malrd1 |
A |
G |
2: 16,106,722 (GRCm39) |
I1845V |
unknown |
Het |
| Mob3c |
G |
A |
4: 115,688,881 (GRCm39) |
R138H |
probably benign |
Het |
| Mre11a |
T |
A |
9: 14,723,209 (GRCm39) |
D394E |
possibly damaging |
Het |
| Myh7b |
A |
T |
2: 155,464,106 (GRCm39) |
I536F |
probably damaging |
Het |
| Nacad |
T |
A |
11: 6,548,589 (GRCm39) |
K1382* |
probably null |
Het |
| Ncor1 |
T |
C |
11: 62,275,598 (GRCm39) |
K128R |
possibly damaging |
Het |
| Or10am5 |
T |
C |
7: 6,517,520 (GRCm39) |
N303D |
probably damaging |
Het |
| Ostn |
T |
A |
16: 27,165,719 (GRCm39) |
|
probably null |
Het |
| Pacs1 |
G |
A |
19: 5,189,003 (GRCm39) |
T793I |
probably damaging |
Het |
| Pcdhb2 |
T |
C |
18: 37,429,547 (GRCm39) |
S507P |
probably damaging |
Het |
| Pde2a |
A |
G |
7: 101,152,597 (GRCm39) |
K393E |
possibly damaging |
Het |
| Pfkl |
T |
A |
10: 77,825,423 (GRCm39) |
N656Y |
probably damaging |
Het |
| Phf20 |
T |
A |
2: 156,135,331 (GRCm39) |
|
probably null |
Het |
| Plekha6 |
G |
T |
1: 133,203,586 (GRCm39) |
E550* |
probably null |
Het |
| Plxna4 |
A |
T |
6: 32,139,095 (GRCm39) |
V1691E |
probably damaging |
Het |
| Rag1 |
A |
T |
2: 101,472,123 (GRCm39) |
H1006Q |
probably damaging |
Het |
| Rfx4 |
C |
T |
10: 84,740,919 (GRCm39) |
P679L |
probably benign |
Het |
| Ripor2 |
A |
G |
13: 24,878,128 (GRCm39) |
H301R |
probably damaging |
Het |
| Rrp12 |
A |
T |
19: 41,871,877 (GRCm39) |
I469N |
possibly damaging |
Het |
| Serpinb6b |
A |
G |
13: 33,161,559 (GRCm39) |
T211A |
probably benign |
Het |
| Sf1 |
A |
T |
19: 6,426,383 (GRCm39) |
H547L |
unknown |
Het |
| Slc29a1 |
T |
C |
17: 45,903,108 (GRCm39) |
D9G |
probably damaging |
Het |
| Sptan1 |
T |
A |
2: 29,892,311 (GRCm39) |
M1075K |
probably benign |
Het |
| Syngap1 |
A |
G |
17: 27,176,741 (GRCm39) |
D474G |
probably damaging |
Het |
| Syt16 |
C |
T |
12: 74,313,483 (GRCm39) |
R470C |
probably damaging |
Het |
| Timeless |
A |
G |
10: 128,087,870 (GRCm39) |
T1148A |
probably benign |
Het |
| Tmem116 |
A |
T |
5: 121,601,899 (GRCm39) |
|
probably null |
Het |
| Tmem158 |
A |
T |
9: 123,089,390 (GRCm39) |
I74N |
probably damaging |
Het |
| Traf5 |
T |
A |
1: 191,743,432 (GRCm39) |
D174V |
probably benign |
Het |
| Trim65 |
A |
T |
11: 116,018,534 (GRCm39) |
I247N |
probably benign |
Het |
| Tsfm |
A |
T |
10: 126,847,500 (GRCm39) |
V197E |
probably benign |
Het |
| Utrn |
A |
G |
10: 12,604,562 (GRCm39) |
C539R |
possibly damaging |
Het |
| Vps13a |
A |
T |
19: 16,655,406 (GRCm39) |
F1874Y |
probably benign |
Het |
| Wdr6 |
A |
G |
9: 108,453,238 (GRCm39) |
M215T |
possibly damaging |
Het |
| Wdr75 |
T |
A |
1: 45,856,560 (GRCm39) |
W528R |
probably damaging |
Het |
| Zc3h7b |
A |
G |
15: 81,655,988 (GRCm39) |
D112G |
possibly damaging |
Het |
| Zc3hav1 |
C |
T |
6: 38,330,911 (GRCm39) |
D83N |
probably benign |
Het |
| Zfp369 |
T |
A |
13: 65,443,931 (GRCm39) |
V358E |
probably damaging |
Het |
| Zfp946 |
T |
A |
17: 22,672,489 (GRCm39) |
C29* |
probably null |
Het |
| Zng1 |
A |
G |
19: 24,898,505 (GRCm39) |
S318P |
probably damaging |
Het |
|
| Other mutations in Btaf1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00392:Btaf1
|
APN |
19 |
36,987,102 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00535:Btaf1
|
APN |
19 |
36,974,935 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00574:Btaf1
|
APN |
19 |
36,947,330 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL00969:Btaf1
|
APN |
19 |
36,988,652 (GRCm39) |
splice site |
probably benign |
|
|
IGL01325:Btaf1
|
APN |
19 |
36,982,049 (GRCm39) |
splice site |
probably benign |
|
|
IGL01399:Btaf1
|
APN |
19 |
36,977,570 (GRCm39) |
nonsense |
probably null |
|
|
IGL02024:Btaf1
|
APN |
19 |
36,969,826 (GRCm39) |
splice site |
probably benign |
|
|
IGL02471:Btaf1
|
APN |
19 |
36,977,592 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL02664:Btaf1
|
APN |
19 |
36,955,828 (GRCm39) |
splice site |
probably benign |
|
|
IGL02898:Btaf1
|
APN |
19 |
36,946,468 (GRCm39) |
missense |
probably benign |
|
|
IGL02995:Btaf1
|
APN |
19 |
36,958,535 (GRCm39) |
splice site |
probably benign |
|
|
IGL03023:Btaf1
|
APN |
19 |
36,987,415 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
IGL03188:Btaf1
|
APN |
19 |
36,926,508 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL03353:Btaf1
|
APN |
19 |
36,969,900 (GRCm39) |
missense |
probably damaging |
1.00 |
|
freudenberg
|
UTSW |
19 |
36,965,573 (GRCm39) |
critical splice donor site |
probably null |
|
|
Galanos
|
UTSW |
19 |
36,926,502 (GRCm39) |
missense |
probably damaging |
1.00 |
|
3-1:Btaf1
|
UTSW |
19 |
36,987,478 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0013:Btaf1
|
UTSW |
19 |
36,935,773 (GRCm39) |
missense |
probably benign |
|
|
R0048:Btaf1
|
UTSW |
19 |
36,980,924 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0117:Btaf1
|
UTSW |
19 |
36,947,368 (GRCm39) |
missense |
probably benign |
0.06 |
|
R0207:Btaf1
|
UTSW |
19 |
36,987,048 (GRCm39) |
nonsense |
probably null |
|
|
R0310:Btaf1
|
UTSW |
19 |
36,981,934 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R0377:Btaf1
|
UTSW |
19 |
36,966,402 (GRCm39) |
missense |
probably benign |
|
|
R0419:Btaf1
|
UTSW |
19 |
36,922,629 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0440:Btaf1
|
UTSW |
19 |
36,964,053 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0532:Btaf1
|
UTSW |
19 |
36,928,586 (GRCm39) |
splice site |
probably benign |
|
|
R0612:Btaf1
|
UTSW |
19 |
36,946,537 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0731:Btaf1
|
UTSW |
19 |
36,974,895 (GRCm39) |
splice site |
probably null |
|
|
R0780:Btaf1
|
UTSW |
19 |
36,966,322 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0919:Btaf1
|
UTSW |
19 |
36,968,143 (GRCm39) |
missense |
probably benign |
0.03 |
|
R1104:Btaf1
|
UTSW |
19 |
36,982,002 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1263:Btaf1
|
UTSW |
19 |
36,933,924 (GRCm39) |
missense |
probably benign |
0.10 |
|
R1325:Btaf1
|
UTSW |
19 |
36,946,562 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R1447:Btaf1
|
UTSW |
19 |
36,969,854 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1554:Btaf1
|
UTSW |
19 |
36,973,998 (GRCm39) |
missense |
probably benign |
0.02 |
|
R1649:Btaf1
|
UTSW |
19 |
36,959,122 (GRCm39) |
missense |
probably benign |
|
|
R1715:Btaf1
|
UTSW |
19 |
36,946,521 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1733:Btaf1
|
UTSW |
19 |
36,972,362 (GRCm39) |
missense |
probably benign |
|
|
R1764:Btaf1
|
UTSW |
19 |
36,928,518 (GRCm39) |
missense |
probably benign |
0.12 |
|
R1874:Btaf1
|
UTSW |
19 |
36,957,983 (GRCm39) |
missense |
probably benign |
|
|
R1911:Btaf1
|
UTSW |
19 |
36,964,030 (GRCm39) |
missense |
probably benign |
|
|
R1933:Btaf1
|
UTSW |
19 |
36,950,357 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2080:Btaf1
|
UTSW |
19 |
36,928,548 (GRCm39) |
missense |
probably benign |
0.09 |
|
R2483:Btaf1
|
UTSW |
19 |
36,958,486 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2510:Btaf1
|
UTSW |
19 |
36,979,845 (GRCm39) |
missense |
probably benign |
0.08 |
|
R3623:Btaf1
|
UTSW |
19 |
36,958,486 (GRCm39) |
missense |
probably benign |
0.02 |
|
R3624:Btaf1
|
UTSW |
19 |
36,958,486 (GRCm39) |
missense |
probably benign |
0.02 |
|
R3801:Btaf1
|
UTSW |
19 |
36,966,373 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3801:Btaf1
|
UTSW |
19 |
36,963,948 (GRCm39) |
missense |
probably benign |
|
|
R3802:Btaf1
|
UTSW |
19 |
36,966,373 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3802:Btaf1
|
UTSW |
19 |
36,963,948 (GRCm39) |
missense |
probably benign |
|
|
R3803:Btaf1
|
UTSW |
19 |
36,966,373 (GRCm39) |
missense |
probably benign |
0.00 |
|
R3803:Btaf1
|
UTSW |
19 |
36,963,948 (GRCm39) |
missense |
probably benign |
|
|
R4077:Btaf1
|
UTSW |
19 |
36,963,879 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4079:Btaf1
|
UTSW |
19 |
36,963,879 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4133:Btaf1
|
UTSW |
19 |
36,939,138 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4673:Btaf1
|
UTSW |
19 |
36,955,772 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4731:Btaf1
|
UTSW |
19 |
36,958,478 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4796:Btaf1
|
UTSW |
19 |
36,933,828 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R4824:Btaf1
|
UTSW |
19 |
36,958,448 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R4835:Btaf1
|
UTSW |
19 |
36,979,858 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4837:Btaf1
|
UTSW |
19 |
36,944,185 (GRCm39) |
missense |
probably benign |
|
|
R4925:Btaf1
|
UTSW |
19 |
36,988,733 (GRCm39) |
missense |
probably benign |
|
|
R4968:Btaf1
|
UTSW |
19 |
36,947,351 (GRCm39) |
missense |
probably null |
0.71 |
|
R4976:Btaf1
|
UTSW |
19 |
36,963,979 (GRCm39) |
missense |
probably benign |
|
|
R5001:Btaf1
|
UTSW |
19 |
36,964,052 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R5037:Btaf1
|
UTSW |
19 |
36,980,931 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5039:Btaf1
|
UTSW |
19 |
36,968,162 (GRCm39) |
missense |
probably benign |
|
|
R5211:Btaf1
|
UTSW |
19 |
36,973,962 (GRCm39) |
missense |
probably benign |
0.32 |
|
R5422:Btaf1
|
UTSW |
19 |
36,928,507 (GRCm39) |
missense |
probably benign |
0.09 |
|
R5429:Btaf1
|
UTSW |
19 |
36,972,257 (GRCm39) |
missense |
possibly damaging |
0.58 |
|
R5530:Btaf1
|
UTSW |
19 |
36,968,175 (GRCm39) |
missense |
possibly damaging |
0.85 |
|
R5582:Btaf1
|
UTSW |
19 |
36,965,573 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5654:Btaf1
|
UTSW |
19 |
36,961,015 (GRCm39) |
missense |
probably benign |
0.35 |
|
R5744:Btaf1
|
UTSW |
19 |
36,981,890 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6082:Btaf1
|
UTSW |
19 |
36,960,942 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6243:Btaf1
|
UTSW |
19 |
36,958,520 (GRCm39) |
missense |
probably benign |
0.02 |
|
R6291:Btaf1
|
UTSW |
19 |
36,950,408 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6502:Btaf1
|
UTSW |
19 |
36,961,017 (GRCm39) |
missense |
probably benign |
|
|
R7034:Btaf1
|
UTSW |
19 |
36,981,869 (GRCm39) |
missense |
probably benign |
|
|
R7036:Btaf1
|
UTSW |
19 |
36,981,869 (GRCm39) |
missense |
probably benign |
|
|
R7085:Btaf1
|
UTSW |
19 |
36,950,318 (GRCm39) |
missense |
probably benign |
|
|
R7097:Btaf1
|
UTSW |
19 |
36,926,502 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7386:Btaf1
|
UTSW |
19 |
36,935,782 (GRCm39) |
missense |
probably benign |
0.02 |
|
R7402:Btaf1
|
UTSW |
19 |
36,980,915 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7452:Btaf1
|
UTSW |
19 |
36,946,527 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7493:Btaf1
|
UTSW |
19 |
36,987,005 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7513:Btaf1
|
UTSW |
19 |
36,955,803 (GRCm39) |
missense |
probably benign |
0.30 |
|
R7888:Btaf1
|
UTSW |
19 |
36,943,036 (GRCm39) |
missense |
probably benign |
0.10 |
|
R7944:Btaf1
|
UTSW |
19 |
36,926,565 (GRCm39) |
missense |
probably benign |
|
|
R8062:Btaf1
|
UTSW |
19 |
36,969,865 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8559:Btaf1
|
UTSW |
19 |
36,964,273 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8793:Btaf1
|
UTSW |
19 |
36,958,429 (GRCm39) |
missense |
probably benign |
0.21 |
|
R8855:Btaf1
|
UTSW |
19 |
36,935,901 (GRCm39) |
missense |
probably benign |
|
|
R8866:Btaf1
|
UTSW |
19 |
36,935,901 (GRCm39) |
missense |
probably benign |
|
|
R9016:Btaf1
|
UTSW |
19 |
36,971,705 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9028:Btaf1
|
UTSW |
19 |
36,946,508 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9109:Btaf1
|
UTSW |
19 |
36,964,114 (GRCm39) |
missense |
probably benign |
|
|
R9172:Btaf1
|
UTSW |
19 |
36,977,630 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9298:Btaf1
|
UTSW |
19 |
36,964,114 (GRCm39) |
missense |
probably benign |
|
|
R9717:Btaf1
|
UTSW |
19 |
36,922,646 (GRCm39) |
missense |
probably benign |
0.28 |
|
W0251:Btaf1
|
UTSW |
19 |
36,980,904 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0027:Btaf1
|
UTSW |
19 |
36,926,496 (GRCm39) |
nonsense |
probably null |
|
|
Z1088:Btaf1
|
UTSW |
19 |
36,964,018 (GRCm39) |
missense |
probably damaging |
0.99 |
|
| Predicted Primers |
PCR Primer
(F):5'- GTTGAATACATTTTCTGGCTCAAGC -3'
(R):5'- GTCAGACTCAAATTTGTCACACAAG -3'
Sequencing Primer
(F):5'- TCTGGCTCAAGCTTATGAGGAAAC -3'
(R):5'- AAAGTTTCAATATCTGACACATCCC -3'
|
| Posted On |
2019-06-26 |
Incidental Mutation