Incidental Mutation 'R7493:Btaf1'
| ID |
580965 |
| 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 |
045567-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.967)
|
| Stock # |
R7493 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
19 |
| Chromosomal Location |
36903479-36990152 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 36987005 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Phenylalanine
at position 1700
(V1700F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000097093
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000099494]
|
| AlphaFold |
E9QAE3 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000099494
AA Change: V1700F
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000097093
Gene: ENSMUSG00000040565
AA Change: V1700F
| 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 |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 98.9%
|
| Validation Efficiency |
97% (74/76) |
| 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: 77 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 3425401B19Rik |
A |
G |
14: 32,385,257 (GRCm39) |
L236P |
possibly damaging |
Het |
| Abca7 |
T |
A |
10: 79,837,896 (GRCm39) |
D488E |
probably damaging |
Het |
| Adora2a |
A |
G |
10: 75,169,423 (GRCm39) |
K296E |
possibly damaging |
Het |
| Aopep |
A |
G |
13: 63,163,345 (GRCm39) |
D122G |
probably benign |
Het |
| Atp13a4 |
T |
A |
16: 29,290,774 (GRCm39) |
E225V |
|
Het |
| Bpifb2 |
A |
G |
2: 153,731,397 (GRCm39) |
M258V |
possibly damaging |
Het |
| Brd2 |
G |
A |
17: 34,341,231 (GRCm39) |
|
probably benign |
Het |
| C2cd3 |
A |
G |
7: 100,076,433 (GRCm39) |
I797V |
|
Het |
| Ccdc148 |
T |
G |
2: 58,899,160 (GRCm39) |
E71A |
probably damaging |
Het |
| Ccdc18 |
T |
A |
5: 108,354,483 (GRCm39) |
L1074* |
probably null |
Het |
| Ccne2 |
A |
G |
4: 11,198,772 (GRCm39) |
D215G |
probably damaging |
Het |
| Cers6 |
T |
A |
2: 68,692,151 (GRCm39) |
|
probably null |
Het |
| Copz1 |
A |
G |
15: 103,204,971 (GRCm39) |
E110G |
probably damaging |
Het |
| Cped1 |
A |
T |
6: 22,215,512 (GRCm39) |
D682V |
probably damaging |
Het |
| Crb1 |
A |
T |
1: 139,164,768 (GRCm39) |
C1180S |
probably damaging |
Het |
| Cyren |
A |
T |
6: 34,851,593 (GRCm39) |
L114Q |
probably damaging |
Het |
| Echdc3 |
A |
T |
2: 6,194,368 (GRCm39) |
L229Q |
probably damaging |
Het |
| Etfb |
C |
T |
7: 43,104,000 (GRCm39) |
P145L |
probably damaging |
Het |
| Exoc3l2 |
G |
T |
7: 19,203,813 (GRCm39) |
R135L |
|
Het |
| Fam83a |
G |
A |
15: 57,849,569 (GRCm39) |
A38T |
probably damaging |
Het |
| G6pc2 |
T |
C |
2: 69,053,344 (GRCm39) |
Y133H |
probably benign |
Het |
| Gfy |
T |
C |
7: 44,827,518 (GRCm39) |
I193V |
probably benign |
Het |
| Ggnbp2 |
T |
C |
11: 84,744,899 (GRCm39) |
T208A |
probably benign |
Het |
| Gigyf1 |
T |
A |
5: 137,523,795 (GRCm39) |
M1019K |
probably damaging |
Het |
| Gm45783 |
T |
C |
7: 7,373,599 (GRCm39) |
D61G |
probably damaging |
Het |
| Golga5 |
T |
C |
12: 102,450,835 (GRCm39) |
|
probably null |
Het |
| Ighe |
A |
G |
12: 113,235,023 (GRCm39) |
V379A |
|
Het |
| Itpr3 |
C |
A |
17: 27,313,774 (GRCm39) |
H573Q |
probably benign |
Het |
| Klhl2 |
A |
G |
8: 65,202,809 (GRCm39) |
L463P |
probably damaging |
Het |
| Large1 |
T |
G |
8: 73,550,343 (GRCm39) |
M619L |
probably benign |
Het |
| Limd1 |
T |
A |
9: 123,308,748 (GRCm39) |
V149E |
probably benign |
Het |
| Lyz2 |
T |
C |
10: 117,118,144 (GRCm39) |
K2E |
probably damaging |
Het |
| Man2c1 |
T |
A |
9: 57,048,412 (GRCm39) |
S858T |
probably damaging |
Het |
| Nt5dc1 |
A |
T |
10: 34,180,932 (GRCm39) |
N439K |
probably benign |
Het |
| Or4a2 |
A |
G |
2: 89,248,145 (GRCm39) |
I204T |
probably benign |
Het |
| Or4n4b |
G |
A |
14: 50,536,281 (GRCm39) |
L162F |
probably benign |
Het |
| Or4p7 |
T |
C |
2: 88,222,224 (GRCm39) |
V211A |
possibly damaging |
Het |
| Or51f1 |
A |
T |
7: 102,506,278 (GRCm39) |
Y70* |
probably null |
Het |
| Or5d43 |
T |
C |
2: 88,105,445 (GRCm39) |
|
probably benign |
Het |
| Or7g27 |
A |
C |
9: 19,250,109 (GRCm39) |
M118L |
probably damaging |
Het |
| Otogl |
T |
C |
10: 107,722,843 (GRCm39) |
N296S |
probably benign |
Het |
| Patj |
A |
G |
4: 98,383,298 (GRCm39) |
N789D |
probably benign |
Het |
| Pcsk6 |
A |
G |
7: 65,693,314 (GRCm39) |
D851G |
possibly damaging |
Het |
| Peg3 |
T |
C |
7: 6,712,723 (GRCm39) |
H833R |
probably damaging |
Het |
| Pira1 |
T |
C |
7: 3,742,023 (GRCm39) |
E119G |
not run |
Het |
| Plekha5 |
A |
G |
6: 140,526,161 (GRCm39) |
D933G |
probably benign |
Het |
| Pnma1 |
G |
A |
12: 84,193,903 (GRCm39) |
R267C |
probably damaging |
Het |
| Ppp3cb |
T |
A |
14: 20,558,619 (GRCm39) |
H481L |
probably benign |
Het |
| Prl8a8 |
T |
C |
13: 27,695,418 (GRCm39) |
|
probably null |
Het |
| Ptma |
GGAAGAAG |
GGAAGAAGAAG |
1: 86,457,261 (GRCm39) |
|
probably benign |
Het |
| Ptpro |
C |
A |
6: 137,359,647 (GRCm39) |
L406I |
probably benign |
Het |
| Rbpj |
T |
C |
5: 53,758,276 (GRCm39) |
S18P |
probably benign |
Het |
| Rhbg |
C |
T |
3: 88,154,886 (GRCm39) |
V173M |
probably damaging |
Het |
| Rps6kc1 |
A |
G |
1: 190,532,254 (GRCm39) |
S583P |
probably benign |
Het |
| Ryr1 |
T |
C |
7: 28,794,630 (GRCm39) |
S1217G |
probably benign |
Het |
| S1pr1 |
A |
T |
3: 115,505,922 (GRCm39) |
I224N |
probably damaging |
Het |
| Sall1 |
C |
T |
8: 89,757,681 (GRCm39) |
D808N |
probably benign |
Het |
| Shoc2 |
T |
C |
19: 53,976,467 (GRCm39) |
V119A |
probably benign |
Het |
| Spata31h1 |
A |
T |
10: 82,124,798 (GRCm39) |
Y2737* |
probably null |
Het |
| Spata31h1 |
T |
C |
10: 82,152,264 (GRCm39) |
Y34C |
unknown |
Het |
| Ssh2 |
A |
T |
11: 77,328,542 (GRCm39) |
E369D |
probably benign |
Het |
| Stx1b |
C |
T |
7: 127,406,531 (GRCm39) |
V273M |
possibly damaging |
Het |
| Syne2 |
A |
G |
12: 76,012,654 (GRCm39) |
H2615R |
probably benign |
Het |
| Tmc8 |
T |
C |
11: 117,675,758 (GRCm39) |
I225T |
probably benign |
Het |
| Tmem126b |
A |
G |
7: 90,121,854 (GRCm39) |
I52T |
probably benign |
Het |
| Top2b |
G |
A |
14: 16,416,605 (GRCm38) |
D1122N |
probably benign |
Het |
| Trav13-2 |
T |
A |
14: 53,872,363 (GRCm39) |
S7T |
possibly damaging |
Het |
| Ttc1 |
A |
T |
11: 43,636,189 (GRCm39) |
L18Q |
probably damaging |
Het |
| Ttn |
A |
T |
2: 76,567,553 (GRCm39) |
I27780N |
probably damaging |
Het |
| Ubfd1 |
T |
C |
7: 121,666,635 (GRCm39) |
S44P |
probably benign |
Het |
| Vmn1r89 |
A |
G |
7: 12,953,632 (GRCm39) |
K123E |
probably damaging |
Het |
| Vmn2r62 |
A |
C |
7: 42,437,316 (GRCm39) |
F389L |
possibly damaging |
Het |
| Vps35l |
C |
T |
7: 118,393,800 (GRCm39) |
|
probably null |
Het |
| Zdhhc11 |
T |
A |
13: 74,121,726 (GRCm39) |
M79K |
possibly damaging |
Het |
| Zfp202 |
G |
T |
9: 40,118,640 (GRCm39) |
V18F |
possibly damaging |
Het |
| Zfp39 |
A |
G |
11: 58,781,869 (GRCm39) |
F298L |
possibly damaging |
Het |
| Znrf1 |
G |
A |
8: 112,264,071 (GRCm39) |
G100D |
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 |
|
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 |
|
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'- GGACATTCTCATCTCAGTGGATAAC -3'
(R):5'- TCGCTGAGGTGAAAGAGCAC -3'
Sequencing Primer
(F):5'- CTTGACACAAGCTAGAGTTGC -3'
(R):5'- GTGAAAGAGCACTGGCACCC -3'
|
| Posted On |
2019-10-17 |
Incidental Mutation