Incidental Mutation 'R0207:Btaf1'
| ID |
33439 |
| 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 |
038460-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.965)
|
| Stock # |
R0207 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
19 |
| Chromosomal Location |
36903479-36990152 bp(+) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
T to A
at 36987048 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Stop codon
at position 1714
(L1714*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000097093
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099494]
|
| AlphaFold |
E9QAE3 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000099494
AA Change: L1714*
|
| SMART Domains |
Protein: ENSMUSP00000097093
Gene: ENSMUSG00000040565
AA Change: L1714*
| 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 |
0.9755 |
| Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.7%
- 10x: 97.2%
- 20x: 95.5%
|
| Validation Efficiency |
95% (76/80) |
| 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: 82 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca1 |
A |
G |
4: 53,086,039 (GRCm39) |
F488S |
probably damaging |
Het |
| Acap3 |
C |
T |
4: 155,983,881 (GRCm39) |
R116W |
probably damaging |
Het |
| Adamts10 |
C |
A |
17: 33,764,364 (GRCm39) |
P663T |
possibly damaging |
Het |
| Akap12 |
G |
A |
10: 4,303,333 (GRCm39) |
G48S |
probably damaging |
Het |
| Ankrd7 |
T |
A |
6: 18,870,030 (GRCm39) |
M261K |
probably benign |
Het |
| Ankzf1 |
C |
A |
1: 75,174,948 (GRCm39) |
D599E |
possibly damaging |
Het |
| Aox1 |
T |
C |
1: 58,144,173 (GRCm39) |
I1278T |
possibly damaging |
Het |
| Apcdd1 |
T |
C |
18: 63,083,150 (GRCm39) |
Y327H |
probably benign |
Het |
| Asxl3 |
T |
A |
18: 22,544,553 (GRCm39) |
|
probably benign |
Het |
| Birc6 |
C |
A |
17: 74,969,827 (GRCm39) |
|
probably benign |
Het |
| Cacng6 |
T |
A |
7: 3,473,520 (GRCm39) |
|
probably benign |
Het |
| Cdc20b |
A |
G |
13: 113,215,146 (GRCm39) |
D238G |
probably damaging |
Het |
| Celf5 |
T |
A |
10: 81,306,532 (GRCm39) |
R113W |
probably null |
Het |
| Cfap251 |
T |
C |
5: 123,421,510 (GRCm39) |
V182A |
probably damaging |
Het |
| Cfap70 |
C |
A |
14: 20,462,415 (GRCm39) |
E659D |
probably damaging |
Het |
| Clspn |
T |
A |
4: 126,484,391 (GRCm39) |
M1183K |
possibly damaging |
Het |
| Dpy19l1 |
G |
A |
9: 24,365,187 (GRCm39) |
R275C |
probably damaging |
Het |
| Dst |
C |
T |
1: 34,226,016 (GRCm39) |
S1721L |
probably benign |
Het |
| Faap100 |
T |
C |
11: 120,265,191 (GRCm39) |
T562A |
probably damaging |
Het |
| Fam168b |
T |
C |
1: 34,858,769 (GRCm39) |
M133V |
probably damaging |
Het |
| Farp2 |
T |
C |
1: 93,496,809 (GRCm39) |
I172T |
probably damaging |
Het |
| Fer |
T |
G |
17: 64,203,273 (GRCm39) |
S68A |
probably damaging |
Het |
| Fmo5 |
A |
G |
3: 97,552,997 (GRCm39) |
E315G |
probably damaging |
Het |
| Gpr89 |
A |
T |
3: 96,778,796 (GRCm39) |
F426I |
probably damaging |
Het |
| Hinfp |
T |
C |
9: 44,207,624 (GRCm39) |
I461V |
possibly damaging |
Het |
| Hsd11b1 |
A |
T |
1: 192,922,556 (GRCm39) |
V167D |
probably damaging |
Het |
| Htt |
A |
G |
5: 35,054,252 (GRCm39) |
K2574E |
probably benign |
Het |
| I830077J02Rik |
A |
G |
3: 105,833,821 (GRCm39) |
S112P |
probably benign |
Het |
| Igf2bp3 |
T |
A |
6: 49,082,551 (GRCm39) |
M344L |
probably benign |
Het |
| Itch |
A |
T |
2: 155,044,177 (GRCm39) |
Q494L |
probably benign |
Het |
| Itga9 |
T |
C |
9: 118,598,321 (GRCm39) |
|
probably benign |
Het |
| Jaml |
T |
A |
9: 45,005,065 (GRCm39) |
D152E |
probably benign |
Het |
| Kif22 |
A |
C |
7: 126,641,572 (GRCm39) |
M1R |
probably null |
Het |
| Kifap3 |
T |
C |
1: 163,710,955 (GRCm39) |
Y663H |
probably benign |
Het |
| Letm2 |
T |
A |
8: 26,068,786 (GRCm39) |
N472I |
probably damaging |
Het |
| Mthfr |
T |
G |
4: 148,136,681 (GRCm39) |
V446G |
probably damaging |
Het |
| Myh11 |
T |
C |
16: 14,029,124 (GRCm39) |
E1206G |
possibly damaging |
Het |
| Myo6 |
G |
A |
9: 80,195,338 (GRCm39) |
V903I |
probably damaging |
Het |
| Myo9b |
C |
T |
8: 71,807,869 (GRCm39) |
|
probably benign |
Het |
| Nr2f2 |
G |
C |
7: 70,009,923 (GRCm39) |
P52R |
probably damaging |
Het |
| Nsd3 |
A |
G |
8: 26,173,273 (GRCm39) |
N859S |
probably benign |
Het |
| Nucb2 |
C |
A |
7: 116,135,245 (GRCm39) |
A384E |
probably damaging |
Het |
| Ogdhl |
C |
A |
14: 32,063,994 (GRCm39) |
|
probably null |
Het |
| Or10al3 |
C |
A |
17: 38,011,949 (GRCm39) |
C129* |
probably null |
Het |
| Or1e22 |
A |
T |
11: 73,377,401 (GRCm39) |
L83Q |
probably benign |
Het |
| Or1i2 |
T |
C |
10: 78,447,705 (GRCm39) |
T257A |
probably benign |
Het |
| Or4a74 |
G |
A |
2: 89,440,207 (GRCm39) |
L80F |
probably damaging |
Het |
| Or5b105 |
G |
A |
19: 13,080,642 (GRCm39) |
R3C |
possibly damaging |
Het |
| Parp10 |
C |
T |
15: 76,126,833 (GRCm39) |
S145N |
probably benign |
Het |
| Pigh |
A |
G |
12: 79,130,483 (GRCm39) |
|
probably benign |
Het |
| Pigo |
A |
G |
4: 43,023,824 (GRCm39) |
|
probably benign |
Het |
| Pkp4 |
T |
A |
2: 59,135,832 (GRCm39) |
V199D |
possibly damaging |
Het |
| Polr1e |
C |
A |
4: 45,025,143 (GRCm39) |
|
probably null |
Het |
| Ppfia3 |
C |
A |
7: 44,997,958 (GRCm39) |
R723L |
probably damaging |
Het |
| Prex1 |
C |
A |
2: 166,427,818 (GRCm39) |
A945S |
possibly damaging |
Het |
| Prrt3 |
A |
T |
6: 113,472,801 (GRCm39) |
V457E |
probably damaging |
Het |
| Rab39 |
A |
G |
9: 53,617,271 (GRCm39) |
F49L |
possibly damaging |
Het |
| Rrs1 |
C |
A |
1: 9,615,987 (GRCm39) |
|
probably null |
Het |
| Rrs1 |
G |
A |
1: 9,615,992 (GRCm39) |
E82K |
probably damaging |
Het |
| Serpinb3c |
T |
C |
1: 107,204,722 (GRCm39) |
D8G |
probably benign |
Het |
| Slc17a6 |
A |
G |
7: 51,295,928 (GRCm39) |
|
probably benign |
Het |
| Slc24a4 |
T |
A |
12: 102,195,210 (GRCm39) |
|
probably null |
Het |
| Smc1b |
C |
T |
15: 85,007,960 (GRCm39) |
M272I |
probably benign |
Het |
| Smc6 |
T |
C |
12: 11,333,179 (GRCm39) |
|
probably benign |
Het |
| Tcf20 |
T |
C |
15: 82,739,286 (GRCm39) |
T722A |
probably benign |
Het |
| Tesmin |
A |
T |
19: 3,454,088 (GRCm39) |
M141L |
probably benign |
Het |
| Tmprss5 |
T |
A |
9: 49,024,460 (GRCm39) |
H274Q |
possibly damaging |
Het |
| Tns1 |
C |
T |
1: 73,976,477 (GRCm39) |
|
probably null |
Het |
| Tpr |
T |
C |
1: 150,293,178 (GRCm39) |
S868P |
possibly damaging |
Het |
| Trank1 |
C |
T |
9: 111,195,321 (GRCm39) |
T1115I |
probably damaging |
Het |
| Trmt44 |
A |
T |
5: 35,730,261 (GRCm39) |
I203K |
possibly damaging |
Het |
| Ulk2 |
A |
T |
11: 61,668,611 (GRCm39) |
V1037E |
probably benign |
Het |
| Usp43 |
A |
G |
11: 67,767,325 (GRCm39) |
Y682H |
probably damaging |
Het |
| Vipr2 |
A |
T |
12: 116,106,502 (GRCm39) |
Q366L |
probably damaging |
Het |
| Vmn1r185 |
C |
A |
7: 26,311,014 (GRCm39) |
V164L |
possibly damaging |
Het |
| Vmn2r120 |
C |
T |
17: 57,832,052 (GRCm39) |
V246I |
probably benign |
Het |
| Wiz |
C |
T |
17: 32,576,007 (GRCm39) |
G790R |
probably damaging |
Het |
| Wnk1 |
A |
T |
6: 119,929,694 (GRCm39) |
S1016R |
probably damaging |
Het |
| Zc3hav1 |
A |
G |
6: 38,288,109 (GRCm39) |
L909S |
probably benign |
Het |
| Zfp236 |
T |
A |
18: 82,658,352 (GRCm39) |
I637F |
probably damaging |
Het |
| Zfp788 |
G |
A |
7: 41,299,020 (GRCm39) |
G532D |
probably damaging |
Het |
| Zranb1 |
T |
C |
7: 132,552,114 (GRCm39) |
I255T |
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 |
|
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 |
|
R7248:Btaf1
|
UTSW |
19 |
36,922,714 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
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'- AAATACACAGTAacagttcaagggcaca -3'
(R):5'- CAACATAGAGACAGTGACCCAGGC -3'
Sequencing Primer
(F):5'- gtaagccaggaggagcaag -3'
(R):5'- AGACAGTGACCCAGGCTTTTG -3'
|
| Posted On |
2013-05-09 |
Incidental Mutation