Incidental Mutation 'R4757:Phf3'
| ID |
500061 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Phf3
|
| Ensembl Gene |
ENSMUSG00000048874 |
| Gene Name |
PHD finger protein 3 |
| Synonyms |
AU020177, 2310061N19Rik |
| MMRRC Submission |
041973-MU
|
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
R4757 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
30841417-30912989 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 30859908 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glycine to Aspartic acid
at position 873
(G873D)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000139610
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000088310]
[ENSMUST00000186733]
[ENSMUST00000191064]
|
| AlphaFold |
B2RQG2 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000088310
AA Change: G873D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000085650
Gene: ENSMUSG00000048874
AA Change: G873D
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
212 |
223 |
N/A |
INTRINSIC |
|
low complexity region
|
337 |
344 |
N/A |
INTRINSIC |
|
low complexity region
|
600 |
611 |
N/A |
INTRINSIC |
|
low complexity region
|
651 |
660 |
N/A |
INTRINSIC |
|
PHD
|
697 |
748 |
3.82e-10 |
SMART |
|
low complexity region
|
847 |
859 |
N/A |
INTRINSIC |
|
low complexity region
|
876 |
887 |
N/A |
INTRINSIC |
|
TFS2M
|
908 |
1008 |
1.28e-47 |
SMART |
|
Pfam:SPOC
|
1188 |
1294 |
4.2e-26 |
PFAM |
|
low complexity region
|
1367 |
1373 |
N/A |
INTRINSIC |
|
low complexity region
|
1516 |
1529 |
N/A |
INTRINSIC |
|
low complexity region
|
1597 |
1620 |
N/A |
INTRINSIC |
|
low complexity region
|
1796 |
1811 |
N/A |
INTRINSIC |
|
low complexity region
|
1813 |
1846 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000186105
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000186733
AA Change: G873D
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000139610
Gene: ENSMUSG00000048874
AA Change: G873D
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
212 |
223 |
N/A |
INTRINSIC |
|
low complexity region
|
337 |
344 |
N/A |
INTRINSIC |
|
low complexity region
|
600 |
611 |
N/A |
INTRINSIC |
|
low complexity region
|
651 |
660 |
N/A |
INTRINSIC |
|
PHD
|
697 |
748 |
3.82e-10 |
SMART |
|
low complexity region
|
847 |
859 |
N/A |
INTRINSIC |
|
low complexity region
|
876 |
887 |
N/A |
INTRINSIC |
|
TFS2M
|
908 |
1008 |
1.28e-47 |
SMART |
|
Pfam:SPOC
|
1188 |
1294 |
4.2e-26 |
PFAM |
|
low complexity region
|
1367 |
1373 |
N/A |
INTRINSIC |
|
low complexity region
|
1516 |
1529 |
N/A |
INTRINSIC |
|
low complexity region
|
1597 |
1620 |
N/A |
INTRINSIC |
|
low complexity region
|
1796 |
1811 |
N/A |
INTRINSIC |
|
low complexity region
|
1813 |
1846 |
N/A |
INTRINSIC |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000187600
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000188847
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000191064
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000191245
|
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.5%
- 10x: 97.0%
- 20x: 94.5%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of a PHD finger-containing gene family. This gene may function as a transcription factor and may be involved in glioblastomas development. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2014]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 76 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 4930550C14Rik |
A |
T |
9: 53,336,830 (GRCm39) |
M45L |
probably benign |
Het |
| Abcb1a |
T |
A |
5: 8,787,632 (GRCm39) |
V978D |
probably damaging |
Het |
| Acsm4 |
T |
C |
7: 119,297,900 (GRCm39) |
V179A |
probably benign |
Het |
| Agtr1a |
C |
A |
13: 30,565,842 (GRCm39) |
Y302* |
probably null |
Het |
| Akap9 |
T |
C |
5: 4,058,382 (GRCm39) |
I1677T |
probably damaging |
Het |
| Ankk1 |
T |
A |
9: 49,327,230 (GRCm39) |
M650L |
probably benign |
Het |
| Apod |
T |
A |
16: 31,122,280 (GRCm39) |
N65Y |
probably damaging |
Het |
| Bcl2l1 |
T |
A |
2: 152,624,178 (GRCm39) |
N197Y |
possibly damaging |
Het |
| Brpf1 |
A |
T |
6: 113,292,072 (GRCm39) |
I373F |
probably damaging |
Het |
| Car13 |
T |
C |
3: 14,726,615 (GRCm39) |
V257A |
probably damaging |
Het |
| Ccdc150 |
A |
T |
1: 54,317,874 (GRCm39) |
H271L |
possibly damaging |
Het |
| Cit |
T |
A |
5: 116,135,608 (GRCm39) |
I1836N |
probably damaging |
Het |
| Clec12b |
A |
G |
6: 129,357,655 (GRCm39) |
S68P |
probably damaging |
Het |
| Col4a4 |
A |
G |
1: 82,506,187 (GRCm39) |
F298L |
unknown |
Het |
| Crct1 |
G |
A |
3: 92,922,093 (GRCm39) |
Q15* |
probably null |
Het |
| Creld1 |
A |
G |
6: 113,469,208 (GRCm39) |
E346G |
probably benign |
Het |
| Ctnnal1 |
T |
A |
4: 56,847,980 (GRCm39) |
H53L |
probably damaging |
Het |
| Cyb5d1 |
T |
C |
11: 69,285,814 (GRCm39) |
D74G |
probably damaging |
Het |
| Deptor |
A |
T |
15: 55,075,674 (GRCm39) |
S293C |
probably damaging |
Het |
| Dnajb12 |
A |
G |
10: 59,728,592 (GRCm39) |
S187G |
probably benign |
Het |
| Duoxa2 |
G |
T |
2: 122,131,072 (GRCm39) |
V78L |
possibly damaging |
Het |
| Fem1al |
A |
T |
11: 29,775,454 (GRCm39) |
M1K |
probably null |
Het |
| Fhod1 |
C |
A |
8: 106,074,443 (GRCm39) |
|
probably benign |
Het |
| Foxf2 |
C |
T |
13: 31,810,172 (GRCm39) |
P37L |
unknown |
Het |
| Gabbr2 |
T |
C |
4: 46,875,675 (GRCm39) |
N149S |
probably damaging |
Het |
| Gckr |
G |
T |
5: 31,464,728 (GRCm39) |
M344I |
possibly damaging |
Het |
| Herc6 |
G |
A |
6: 57,577,045 (GRCm39) |
|
probably null |
Het |
| Igf1 |
A |
T |
10: 87,751,287 (GRCm39) |
E161V |
probably benign |
Het |
| Ighv8-13 |
T |
A |
12: 115,729,268 (GRCm39) |
|
probably benign |
Het |
| Igkv6-14 |
A |
T |
6: 70,412,426 (GRCm39) |
L12* |
probably null |
Het |
| Kpnb1 |
C |
T |
11: 97,068,160 (GRCm39) |
S270N |
possibly damaging |
Het |
| Lingo1 |
A |
G |
9: 56,527,209 (GRCm39) |
V460A |
probably benign |
Het |
| Lsm6 |
T |
C |
8: 79,539,711 (GRCm39) |
|
probably null |
Het |
| Mccc1 |
C |
T |
3: 36,050,066 (GRCm39) |
G42E |
probably benign |
Het |
| Mga |
A |
G |
2: 119,734,120 (GRCm39) |
K323E |
possibly damaging |
Het |
| Mks1 |
A |
G |
11: 87,753,850 (GRCm39) |
*562W |
probably null |
Het |
| Mrgpra4 |
T |
A |
7: 47,630,686 (GRCm39) |
E305V |
probably damaging |
Het |
| Msh4 |
T |
A |
3: 153,585,024 (GRCm39) |
H360L |
probably damaging |
Het |
| Mthfsd |
C |
T |
8: 121,825,737 (GRCm39) |
|
probably null |
Het |
| Myl12a |
A |
T |
17: 71,303,798 (GRCm39) |
F26L |
possibly damaging |
Het |
| Nedd4l |
A |
G |
18: 65,298,676 (GRCm39) |
S343G |
probably damaging |
Het |
| Nlgn1 |
T |
A |
3: 25,490,332 (GRCm39) |
D465V |
probably damaging |
Het |
| Nlgn1 |
C |
T |
3: 25,490,507 (GRCm39) |
V407I |
possibly damaging |
Het |
| Npsr1 |
T |
C |
9: 24,046,064 (GRCm39) |
V61A |
probably benign |
Het |
| Nrxn2 |
A |
G |
19: 6,559,851 (GRCm39) |
D160G |
probably damaging |
Het |
| Or2p2 |
T |
C |
13: 21,256,715 (GRCm39) |
Y252C |
probably damaging |
Het |
| Or52d3 |
T |
C |
7: 104,229,404 (GRCm39) |
Y184H |
possibly damaging |
Het |
| Or5b107 |
A |
C |
19: 13,143,277 (GRCm39) |
S300R |
probably benign |
Het |
| Or5b113 |
G |
T |
19: 13,342,810 (GRCm39) |
A273S |
probably benign |
Het |
| Or9g4 |
A |
G |
2: 85,504,664 (GRCm39) |
F277S |
probably damaging |
Het |
| Pbx1 |
C |
A |
1: 168,023,450 (GRCm39) |
R235L |
probably damaging |
Het |
| Pcnx4 |
T |
C |
12: 72,603,067 (GRCm39) |
V443A |
probably benign |
Het |
| Pde7b |
T |
C |
10: 20,423,688 (GRCm39) |
T63A |
probably benign |
Het |
| Phox2b |
A |
T |
5: 67,256,197 (GRCm39) |
Y30N |
probably damaging |
Het |
| Plch2 |
T |
A |
4: 155,080,690 (GRCm39) |
I599F |
possibly damaging |
Het |
| Plekha8 |
A |
G |
6: 54,599,213 (GRCm39) |
E249G |
probably benign |
Het |
| Pou2af1 |
T |
A |
9: 51,144,439 (GRCm39) |
Y118N |
possibly damaging |
Het |
| Ppp3cc |
T |
A |
14: 70,455,635 (GRCm39) |
K489N |
possibly damaging |
Het |
| Sema4b |
T |
C |
7: 79,866,577 (GRCm39) |
L219P |
probably damaging |
Het |
| Slc6a5 |
T |
G |
7: 49,609,030 (GRCm39) |
V745G |
probably benign |
Het |
| Slf2 |
A |
G |
19: 44,923,497 (GRCm39) |
M104V |
probably benign |
Het |
| Slx1b |
A |
G |
7: 126,291,701 (GRCm39) |
V121A |
probably benign |
Het |
| Speer4e2 |
T |
A |
5: 15,026,222 (GRCm39) |
H145L |
probably benign |
Het |
| Spen |
T |
A |
4: 141,200,390 (GRCm39) |
K2746* |
probably null |
Het |
| Stxbp5l |
T |
C |
16: 37,008,996 (GRCm39) |
Y681C |
probably damaging |
Het |
| Sv2b |
T |
C |
7: 74,773,918 (GRCm39) |
T518A |
probably benign |
Het |
| Tgm7 |
A |
T |
2: 120,926,870 (GRCm39) |
H426Q |
possibly damaging |
Het |
| Tlx2 |
A |
G |
6: 83,046,900 (GRCm39) |
F54S |
probably benign |
Het |
| Trp53bp2 |
A |
T |
1: 182,286,339 (GRCm39) |
M1060L |
probably benign |
Het |
| Trpv5 |
T |
A |
6: 41,630,148 (GRCm39) |
E647D |
probably damaging |
Het |
| Tut1 |
G |
T |
19: 8,936,672 (GRCm39) |
K165N |
possibly damaging |
Het |
| Tyro3 |
A |
G |
2: 119,641,419 (GRCm39) |
K543E |
probably damaging |
Het |
| Vmn2r69 |
T |
A |
7: 85,061,575 (GRCm39) |
Y133F |
probably damaging |
Het |
| Zfhx4 |
T |
A |
3: 5,465,122 (GRCm39) |
V1785D |
possibly damaging |
Het |
| Zfp451 |
A |
G |
1: 33,804,939 (GRCm39) |
L1037P |
probably damaging |
Het |
| Zscan29 |
A |
T |
2: 120,991,392 (GRCm39) |
F799I |
possibly damaging |
Het |
|
| Other mutations in Phf3 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00234:Phf3
|
APN |
1 |
30,850,928 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL00704:Phf3
|
APN |
1 |
30,843,919 (GRCm39) |
missense |
probably benign |
|
|
IGL01147:Phf3
|
APN |
1 |
30,843,250 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01360:Phf3
|
APN |
1 |
30,847,809 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01376:Phf3
|
APN |
1 |
30,869,566 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
IGL01396:Phf3
|
APN |
1 |
30,843,386 (GRCm39) |
nonsense |
probably null |
|
|
IGL01830:Phf3
|
APN |
1 |
30,853,148 (GRCm39) |
nonsense |
probably null |
|
|
IGL02108:Phf3
|
APN |
1 |
30,869,032 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02156:Phf3
|
APN |
1 |
30,847,859 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02576:Phf3
|
APN |
1 |
30,869,117 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03031:Phf3
|
APN |
1 |
30,843,734 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03334:Phf3
|
APN |
1 |
30,844,810 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL03411:Phf3
|
APN |
1 |
30,843,482 (GRCm39) |
missense |
probably damaging |
1.00 |
|
FR4976:Phf3
|
UTSW |
1 |
30,844,104 (GRCm39) |
utr 3 prime |
probably benign |
|
|
PIT4458001:Phf3
|
UTSW |
1 |
30,855,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0037:Phf3
|
UTSW |
1 |
30,843,999 (GRCm39) |
missense |
probably benign |
0.03 |
|
R0052:Phf3
|
UTSW |
1 |
30,847,848 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0114:Phf3
|
UTSW |
1 |
30,844,524 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R0123:Phf3
|
UTSW |
1 |
30,844,146 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0225:Phf3
|
UTSW |
1 |
30,844,146 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0715:Phf3
|
UTSW |
1 |
30,850,919 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0835:Phf3
|
UTSW |
1 |
30,869,632 (GRCm39) |
missense |
probably benign |
0.02 |
|
R0848:Phf3
|
UTSW |
1 |
30,902,253 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1473:Phf3
|
UTSW |
1 |
30,845,021 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1522:Phf3
|
UTSW |
1 |
30,844,729 (GRCm39) |
missense |
probably benign |
0.05 |
|
R1549:Phf3
|
UTSW |
1 |
30,843,923 (GRCm39) |
missense |
probably benign |
0.00 |
|
R1555:Phf3
|
UTSW |
1 |
30,844,958 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R1780:Phf3
|
UTSW |
1 |
30,851,023 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1789:Phf3
|
UTSW |
1 |
30,845,287 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1875:Phf3
|
UTSW |
1 |
30,869,704 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R1912:Phf3
|
UTSW |
1 |
30,843,426 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1957:Phf3
|
UTSW |
1 |
30,870,601 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2019:Phf3
|
UTSW |
1 |
30,850,928 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2259:Phf3
|
UTSW |
1 |
30,843,424 (GRCm39) |
missense |
probably benign |
0.20 |
|
R2305:Phf3
|
UTSW |
1 |
30,844,556 (GRCm39) |
nonsense |
probably null |
|
|
R2345:Phf3
|
UTSW |
1 |
30,844,432 (GRCm39) |
nonsense |
probably null |
|
|
R2424:Phf3
|
UTSW |
1 |
30,845,430 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2497:Phf3
|
UTSW |
1 |
30,869,095 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2504:Phf3
|
UTSW |
1 |
30,849,870 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3522:Phf3
|
UTSW |
1 |
30,844,684 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3816:Phf3
|
UTSW |
1 |
30,844,834 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4152:Phf3
|
UTSW |
1 |
30,870,539 (GRCm39) |
missense |
probably benign |
0.13 |
|
R4403:Phf3
|
UTSW |
1 |
30,843,490 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4658:Phf3
|
UTSW |
1 |
30,902,169 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4663:Phf3
|
UTSW |
1 |
30,860,296 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4669:Phf3
|
UTSW |
1 |
30,869,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4706:Phf3
|
UTSW |
1 |
30,844,687 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4766:Phf3
|
UTSW |
1 |
30,853,020 (GRCm39) |
unclassified |
probably benign |
|
|
R4786:Phf3
|
UTSW |
1 |
30,855,638 (GRCm39) |
nonsense |
probably null |
|
|
R5107:Phf3
|
UTSW |
1 |
30,870,566 (GRCm39) |
missense |
probably benign |
0.03 |
|
R5155:Phf3
|
UTSW |
1 |
30,863,457 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R5310:Phf3
|
UTSW |
1 |
30,842,887 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5823:Phf3
|
UTSW |
1 |
30,843,764 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5944:Phf3
|
UTSW |
1 |
30,859,785 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5979:Phf3
|
UTSW |
1 |
30,844,827 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6007:Phf3
|
UTSW |
1 |
30,843,426 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6024:Phf3
|
UTSW |
1 |
30,902,307 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6072:Phf3
|
UTSW |
1 |
30,869,769 (GRCm39) |
missense |
probably benign |
0.08 |
|
R6533:Phf3
|
UTSW |
1 |
30,845,399 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6649:Phf3
|
UTSW |
1 |
30,844,104 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R6653:Phf3
|
UTSW |
1 |
30,844,104 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R6852:Phf3
|
UTSW |
1 |
30,843,711 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6855:Phf3
|
UTSW |
1 |
30,859,204 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6862:Phf3
|
UTSW |
1 |
30,853,063 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6930:Phf3
|
UTSW |
1 |
30,850,958 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7135:Phf3
|
UTSW |
1 |
30,870,190 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R7323:Phf3
|
UTSW |
1 |
30,852,211 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7352:Phf3
|
UTSW |
1 |
30,843,407 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7455:Phf3
|
UTSW |
1 |
30,876,239 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7549:Phf3
|
UTSW |
1 |
30,870,556 (GRCm39) |
missense |
probably benign |
0.01 |
|
R7609:Phf3
|
UTSW |
1 |
30,844,582 (GRCm39) |
missense |
probably benign |
0.05 |
|
R7720:Phf3
|
UTSW |
1 |
30,868,938 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7745:Phf3
|
UTSW |
1 |
30,843,305 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8134:Phf3
|
UTSW |
1 |
30,863,552 (GRCm39) |
missense |
unknown |
|
|
R8264:Phf3
|
UTSW |
1 |
30,870,138 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R8545:Phf3
|
UTSW |
1 |
30,863,391 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R8821:Phf3
|
UTSW |
1 |
30,860,347 (GRCm39) |
nonsense |
probably null |
|
|
R8831:Phf3
|
UTSW |
1 |
30,860,347 (GRCm39) |
nonsense |
probably null |
|
|
R8873:Phf3
|
UTSW |
1 |
30,843,773 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R9101:Phf3
|
UTSW |
1 |
30,843,026 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R9402:Phf3
|
UTSW |
1 |
30,850,928 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9426:Phf3
|
UTSW |
1 |
30,870,625 (GRCm39) |
nonsense |
probably null |
|
|
R9594:Phf3
|
UTSW |
1 |
30,869,003 (GRCm39) |
missense |
probably benign |
0.07 |
|
R9707:Phf3
|
UTSW |
1 |
30,868,923 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9803:Phf3
|
UTSW |
1 |
30,869,872 (GRCm39) |
missense |
probably benign |
0.16 |
|
Z1177:Phf3
|
UTSW |
1 |
30,851,049 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
Z1177:Phf3
|
UTSW |
1 |
30,844,132 (GRCm39) |
missense |
unknown |
|
|
Z1177:Phf3
|
UTSW |
1 |
30,843,376 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Predicted Primers |
PCR Primer
(F):5'- GCTATTCGACCACTGGCATAAC -3'
(R):5'- GAGACTGCTGGAGATTATGTACTTG -3'
Sequencing Primer
(F):5'- CTGGCATAACAACATGTTACCTTTTC -3'
(R):5'- GCGTACACTTTATGACTCTAGAACC -3'
|
| Posted On |
2017-11-30 |
Incidental Mutation