Incidental Mutation 'R9647:Zgrf1'
| ID |
726779 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Zgrf1
|
| Ensembl Gene |
ENSMUSG00000051278 |
| Gene Name |
zinc finger, GRF-type containing 1 |
| Synonyms |
4930422G04Rik |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.080)
|
| Stock # |
R9647 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
3 |
| Chromosomal Location |
127347138-127411672 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 127355251 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Isoleucine
at position 159
(T159I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000142886
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000043108]
[ENSMUST00000195955]
[ENSMUST00000196141]
[ENSMUST00000199888]
[ENSMUST00000200490]
|
| AlphaFold |
Q0VGT4 |
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000043108
AA Change: T159I
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000044432
Gene: ENSMUSG00000051278
AA Change: T159I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF2439
|
3 |
81 |
3.7e-23 |
PFAM |
|
low complexity region
|
92 |
105 |
N/A |
INTRINSIC |
|
low complexity region
|
628 |
639 |
N/A |
INTRINSIC |
|
low complexity region
|
896 |
906 |
N/A |
INTRINSIC |
|
Pfam:zf-GRF
|
1109 |
1153 |
1.5e-17 |
PFAM |
|
low complexity region
|
1316 |
1328 |
N/A |
INTRINSIC |
|
Pfam:AAA_11
|
1501 |
1608 |
1.6e-21 |
PFAM |
|
Pfam:AAA_12
|
1616 |
1802 |
1.3e-51 |
PFAM |
|
coiled coil region
|
1833 |
1861 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000195955
AA Change: T159I
PolyPhen 2
Score 0.019 (Sensitivity: 0.95; Specificity: 0.80)
|
| SMART Domains |
Protein: ENSMUSP00000142886
Gene: ENSMUSG00000051278
AA Change: T159I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF2439
|
3 |
82 |
1.6e-25 |
PFAM |
|
low complexity region
|
92 |
105 |
N/A |
INTRINSIC |
|
low complexity region
|
628 |
639 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000196141
AA Change: T159I
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000143761
Gene: ENSMUSG00000051278
AA Change: T159I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF2439
|
3 |
81 |
3.7e-23 |
PFAM |
|
low complexity region
|
92 |
105 |
N/A |
INTRINSIC |
|
low complexity region
|
628 |
639 |
N/A |
INTRINSIC |
|
low complexity region
|
896 |
906 |
N/A |
INTRINSIC |
|
Pfam:zf-GRF
|
1109 |
1153 |
1.5e-17 |
PFAM |
|
low complexity region
|
1316 |
1328 |
N/A |
INTRINSIC |
|
Pfam:AAA_11
|
1501 |
1608 |
1.6e-21 |
PFAM |
|
Pfam:AAA_12
|
1616 |
1802 |
1.3e-51 |
PFAM |
|
coiled coil region
|
1833 |
1861 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000199888
AA Change: T159I
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000142693
Gene: ENSMUSG00000051278
AA Change: T159I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF2439
|
3 |
82 |
3.5e-22 |
PFAM |
|
low complexity region
|
92 |
105 |
N/A |
INTRINSIC |
|
low complexity region
|
628 |
639 |
N/A |
INTRINSIC |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000200490
AA Change: T159I
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000143585
Gene: ENSMUSG00000051278
AA Change: T159I
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUF2439
|
3 |
81 |
3.4e-20 |
PFAM |
|
low complexity region
|
92 |
105 |
N/A |
INTRINSIC |
|
low complexity region
|
628 |
639 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 78 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abcc5 |
C |
A |
16: 20,195,310 (GRCm39) |
R729L |
probably benign |
Het |
| Actr3b |
T |
C |
5: 26,037,408 (GRCm39) |
S295P |
probably benign |
Het |
| Alb |
G |
A |
5: 90,620,544 (GRCm39) |
|
probably null |
Het |
| Ank2 |
T |
A |
3: 126,792,623 (GRCm39) |
N756I |
possibly damaging |
Het |
| Ankar |
A |
G |
1: 72,689,307 (GRCm39) |
Y1275H |
probably damaging |
Het |
| Ankrd11 |
C |
T |
8: 123,617,682 (GRCm39) |
A2057T |
probably benign |
Het |
| Birc6 |
G |
A |
17: 74,999,305 (GRCm39) |
V4678M |
probably damaging |
Het |
| Bmpr1a |
A |
G |
14: 34,136,694 (GRCm39) |
V499A |
probably benign |
Het |
| Ccdc142 |
A |
G |
6: 83,079,259 (GRCm39) |
N199D |
probably benign |
Het |
| Ccdc179 |
G |
T |
7: 51,663,311 (GRCm39) |
Y38* |
probably null |
Het |
| Cdhr2 |
A |
T |
13: 54,867,394 (GRCm39) |
M438L |
probably benign |
Het |
| Cfap74 |
A |
T |
4: 155,549,373 (GRCm39) |
Q78L |
unknown |
Het |
| Crocc |
A |
T |
4: 140,774,335 (GRCm39) |
S155T |
probably benign |
Het |
| Depdc5 |
T |
A |
5: 33,081,567 (GRCm39) |
H576Q |
possibly damaging |
Het |
| Dhx30 |
A |
T |
9: 109,922,214 (GRCm39) |
L156Q |
probably damaging |
Het |
| Dido1 |
T |
A |
2: 180,315,068 (GRCm39) |
T795S |
probably benign |
Het |
| Dlx1 |
T |
C |
2: 71,360,476 (GRCm39) |
S47P |
probably benign |
Het |
| Dspp |
G |
A |
5: 104,323,636 (GRCm39) |
A260T |
possibly damaging |
Het |
| Ephx2 |
T |
C |
14: 66,326,957 (GRCm39) |
T413A |
probably benign |
Het |
| Erp44 |
A |
C |
4: 48,205,166 (GRCm39) |
L276V |
probably benign |
Het |
| Fastkd5 |
T |
A |
2: 130,457,729 (GRCm39) |
Q287L |
probably damaging |
Het |
| Foxh1 |
T |
A |
15: 76,553,460 (GRCm39) |
H114L |
possibly damaging |
Het |
| Fry |
A |
T |
5: 150,292,984 (GRCm39) |
L410F |
probably damaging |
Het |
| Gamt |
T |
A |
10: 80,095,672 (GRCm39) |
H86L |
probably damaging |
Het |
| Gdpd5 |
G |
T |
7: 99,104,241 (GRCm39) |
R483L |
probably benign |
Het |
| Gm17067 |
A |
C |
7: 42,357,569 (GRCm39) |
V311G |
probably benign |
Het |
| Gpatch2 |
C |
T |
1: 187,054,542 (GRCm39) |
T422I |
probably damaging |
Het |
| Gpi1 |
A |
G |
7: 33,901,879 (GRCm39) |
I546T |
probably damaging |
Het |
| Gyg1 |
A |
C |
3: 20,177,007 (GRCm39) |
S328A |
probably benign |
Het |
| Heatr1 |
T |
A |
13: 12,441,679 (GRCm39) |
V1491E |
probably benign |
Het |
| Hrob |
A |
T |
11: 102,146,586 (GRCm39) |
Q287H |
possibly damaging |
Het |
| Ildr2 |
T |
C |
1: 166,137,038 (GRCm39) |
S626P |
probably benign |
Het |
| Insr |
T |
G |
8: 3,205,874 (GRCm39) |
E1305A |
probably benign |
Het |
| Iqca1 |
T |
A |
1: 89,998,258 (GRCm39) |
T572S |
probably benign |
Het |
| Kdm4a |
A |
T |
4: 118,003,790 (GRCm39) |
M762K |
probably benign |
Het |
| Kdm4a |
T |
A |
4: 118,017,399 (GRCm39) |
T556S |
probably benign |
Het |
| Lama1 |
A |
G |
17: 68,024,170 (GRCm39) |
I89M |
|
Het |
| Larp7 |
T |
C |
3: 127,334,211 (GRCm39) |
K539E |
probably damaging |
Het |
| Mmadhc |
C |
A |
2: 50,186,482 (GRCm39) |
|
probably benign |
Het |
| Mmp2 |
A |
G |
8: 93,567,114 (GRCm39) |
D478G |
probably damaging |
Het |
| Nat10 |
T |
C |
2: 103,578,538 (GRCm39) |
Q222R |
probably benign |
Het |
| Nlgn1 |
A |
T |
3: 25,488,182 (GRCm39) |
Y718N |
probably damaging |
Het |
| Nlrp5 |
A |
T |
7: 23,107,576 (GRCm39) |
E83V |
probably benign |
Het |
| Odc1 |
T |
C |
12: 17,598,614 (GRCm39) |
V218A |
possibly damaging |
Het |
| Or10al4 |
A |
T |
17: 38,037,796 (GRCm39) |
I294F |
probably damaging |
Het |
| Or11g26 |
G |
C |
14: 50,753,552 (GRCm39) |
R297T |
probably damaging |
Het |
| Or9r3 |
A |
G |
10: 129,948,029 (GRCm39) |
I210T |
probably damaging |
Het |
| Oxsr1 |
G |
A |
9: 119,083,932 (GRCm39) |
S324F |
probably damaging |
Het |
| Pclo |
C |
T |
5: 14,731,788 (GRCm39) |
T304M |
|
Het |
| Pgghg |
A |
G |
7: 140,526,743 (GRCm39) |
R687G |
possibly damaging |
Het |
| Plxna4 |
A |
G |
6: 32,228,044 (GRCm39) |
S521P |
probably damaging |
Het |
| Rasgrp4 |
A |
G |
7: 28,839,917 (GRCm39) |
S172G |
probably damaging |
Het |
| Rora |
A |
G |
9: 69,255,450 (GRCm39) |
D78G |
probably damaging |
Het |
| Sec1 |
G |
T |
7: 45,328,556 (GRCm39) |
R164S |
probably benign |
Het |
| Sesn3 |
A |
G |
9: 14,225,999 (GRCm39) |
N245D |
probably benign |
Het |
| Slc44a5 |
T |
A |
3: 153,953,370 (GRCm39) |
W251R |
possibly damaging |
Het |
| Ssr2 |
T |
C |
3: 88,487,206 (GRCm39) |
V7A |
possibly damaging |
Het |
| Syne2 |
A |
G |
12: 76,151,875 (GRCm39) |
D1912G |
possibly damaging |
Het |
| Tcea2 |
C |
A |
2: 181,322,984 (GRCm39) |
T1N |
probably benign |
Het |
| Tmem131l |
T |
C |
3: 83,836,018 (GRCm39) |
Y697C |
probably damaging |
Het |
| Tmx4 |
T |
C |
2: 134,481,588 (GRCm39) |
M112V |
probably benign |
Het |
| Tom1 |
G |
T |
8: 75,785,495 (GRCm39) |
A330S |
probably benign |
Het |
| Trip4 |
A |
T |
9: 65,765,616 (GRCm39) |
L361* |
probably null |
Het |
| Trmt9b |
T |
C |
8: 36,979,210 (GRCm39) |
I271T |
probably benign |
Het |
| Trp73 |
T |
G |
4: 154,165,788 (GRCm39) |
T142P |
probably damaging |
Het |
| Trpm5 |
T |
A |
7: 142,634,498 (GRCm39) |
D683V |
possibly damaging |
Het |
| Trpm7 |
T |
C |
2: 126,667,562 (GRCm39) |
I810V |
probably damaging |
Het |
| Trps1 |
A |
T |
15: 50,524,944 (GRCm39) |
S995R |
probably benign |
Het |
| Ttn |
C |
A |
2: 76,608,269 (GRCm39) |
E17885* |
probably null |
Het |
| Uggt2 |
A |
T |
14: 119,256,312 (GRCm39) |
Y1120N |
probably damaging |
Het |
| Unc13a |
A |
T |
8: 72,104,882 (GRCm39) |
N793K |
probably damaging |
Het |
| Vcf1 |
T |
C |
11: 113,568,146 (GRCm39) |
D103G |
probably damaging |
Het |
| Vmn2r94 |
T |
C |
17: 18,463,884 (GRCm39) |
H802R |
probably benign |
Het |
| Vmn2r-ps158 |
T |
C |
7: 42,697,171 (GRCm39) |
C743R |
probably damaging |
Het |
| Zdhhc5 |
A |
T |
2: 84,524,750 (GRCm39) |
M190K |
probably benign |
Het |
| Zfp719 |
A |
T |
7: 43,233,602 (GRCm39) |
N7I |
possibly damaging |
Het |
| Zfp735 |
A |
G |
11: 73,580,600 (GRCm39) |
Y33C |
probably damaging |
Het |
| Zzef1 |
A |
T |
11: 72,760,651 (GRCm39) |
T1325S |
probably benign |
Het |
|
| Other mutations in Zgrf1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01088:Zgrf1
|
APN |
3 |
127,381,790 (GRCm39) |
splice site |
probably benign |
|
|
IGL01153:Zgrf1
|
APN |
3 |
127,396,055 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01330:Zgrf1
|
APN |
3 |
127,377,656 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01501:Zgrf1
|
APN |
3 |
127,396,211 (GRCm39) |
splice site |
probably null |
|
|
IGL01827:Zgrf1
|
APN |
3 |
127,409,930 (GRCm39) |
missense |
probably benign |
0.06 |
|
IGL02600:Zgrf1
|
APN |
3 |
127,394,623 (GRCm39) |
splice site |
probably benign |
|
|
IGL03122:Zgrf1
|
APN |
3 |
127,381,782 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
IGL03365:Zgrf1
|
APN |
3 |
127,392,423 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R0015_Zgrf1_014
|
UTSW |
3 |
127,349,046 (GRCm39) |
splice site |
probably benign |
|
|
R1298_Zgrf1_204
|
UTSW |
3 |
127,377,538 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7175_zgrf1_533
|
UTSW |
3 |
127,357,239 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0015:Zgrf1
|
UTSW |
3 |
127,349,046 (GRCm39) |
splice site |
probably benign |
|
|
R0243:Zgrf1
|
UTSW |
3 |
127,409,095 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0468:Zgrf1
|
UTSW |
3 |
127,355,690 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R0497:Zgrf1
|
UTSW |
3 |
127,378,299 (GRCm39) |
splice site |
probably benign |
|
|
R0505:Zgrf1
|
UTSW |
3 |
127,366,887 (GRCm39) |
missense |
probably benign |
0.30 |
|
R0511:Zgrf1
|
UTSW |
3 |
127,378,309 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R0539:Zgrf1
|
UTSW |
3 |
127,408,841 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0617:Zgrf1
|
UTSW |
3 |
127,381,687 (GRCm39) |
missense |
probably benign |
0.39 |
|
R1298:Zgrf1
|
UTSW |
3 |
127,377,538 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R1353:Zgrf1
|
UTSW |
3 |
127,405,452 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1593:Zgrf1
|
UTSW |
3 |
127,354,675 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R1846:Zgrf1
|
UTSW |
3 |
127,409,112 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1912:Zgrf1
|
UTSW |
3 |
127,356,786 (GRCm39) |
missense |
probably benign |
|
|
R2062:Zgrf1
|
UTSW |
3 |
127,406,999 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2064:Zgrf1
|
UTSW |
3 |
127,406,999 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2065:Zgrf1
|
UTSW |
3 |
127,406,999 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2066:Zgrf1
|
UTSW |
3 |
127,406,999 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2067:Zgrf1
|
UTSW |
3 |
127,406,999 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2256:Zgrf1
|
UTSW |
3 |
127,355,646 (GRCm39) |
missense |
probably benign |
0.18 |
|
R2321:Zgrf1
|
UTSW |
3 |
127,356,056 (GRCm39) |
nonsense |
probably null |
|
|
R2381:Zgrf1
|
UTSW |
3 |
127,349,863 (GRCm39) |
missense |
probably benign |
0.02 |
|
R2913:Zgrf1
|
UTSW |
3 |
127,392,356 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R3147:Zgrf1
|
UTSW |
3 |
127,377,797 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R3236:Zgrf1
|
UTSW |
3 |
127,407,024 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3237:Zgrf1
|
UTSW |
3 |
127,407,024 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4433:Zgrf1
|
UTSW |
3 |
127,355,727 (GRCm39) |
missense |
probably benign |
|
|
R4441:Zgrf1
|
UTSW |
3 |
127,379,786 (GRCm39) |
missense |
possibly damaging |
0.45 |
|
R4457:Zgrf1
|
UTSW |
3 |
127,389,578 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4498:Zgrf1
|
UTSW |
3 |
127,379,749 (GRCm39) |
nonsense |
probably null |
|
|
R4598:Zgrf1
|
UTSW |
3 |
127,394,679 (GRCm39) |
missense |
probably benign |
0.14 |
|
R4701:Zgrf1
|
UTSW |
3 |
127,392,353 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4898:Zgrf1
|
UTSW |
3 |
127,396,085 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4944:Zgrf1
|
UTSW |
3 |
127,355,517 (GRCm39) |
nonsense |
probably null |
|
|
R5256:Zgrf1
|
UTSW |
3 |
127,396,094 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5294:Zgrf1
|
UTSW |
3 |
127,394,629 (GRCm39) |
missense |
probably benign |
0.14 |
|
R5358:Zgrf1
|
UTSW |
3 |
127,361,352 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5359:Zgrf1
|
UTSW |
3 |
127,394,814 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5447:Zgrf1
|
UTSW |
3 |
127,356,768 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
R5569:Zgrf1
|
UTSW |
3 |
127,354,674 (GRCm39) |
missense |
probably benign |
0.33 |
|
R5887:Zgrf1
|
UTSW |
3 |
127,378,414 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5914:Zgrf1
|
UTSW |
3 |
127,354,672 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5925:Zgrf1
|
UTSW |
3 |
127,366,853 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R5936:Zgrf1
|
UTSW |
3 |
127,355,902 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
R6087:Zgrf1
|
UTSW |
3 |
127,409,135 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6089:Zgrf1
|
UTSW |
3 |
127,389,642 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6181:Zgrf1
|
UTSW |
3 |
127,381,590 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6277:Zgrf1
|
UTSW |
3 |
127,392,461 (GRCm39) |
missense |
possibly damaging |
0.81 |
|
R6441:Zgrf1
|
UTSW |
3 |
127,381,683 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
R6659:Zgrf1
|
UTSW |
3 |
127,410,155 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6857:Zgrf1
|
UTSW |
3 |
127,375,096 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6932:Zgrf1
|
UTSW |
3 |
127,353,281 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7008:Zgrf1
|
UTSW |
3 |
127,355,421 (GRCm39) |
missense |
probably benign |
0.18 |
|
R7175:Zgrf1
|
UTSW |
3 |
127,357,239 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7264:Zgrf1
|
UTSW |
3 |
127,357,218 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7272:Zgrf1
|
UTSW |
3 |
127,392,409 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7298:Zgrf1
|
UTSW |
3 |
127,377,299 (GRCm39) |
nonsense |
probably null |
|
|
R7412:Zgrf1
|
UTSW |
3 |
127,356,720 (GRCm39) |
missense |
probably benign |
0.06 |
|
R7836:Zgrf1
|
UTSW |
3 |
127,357,080 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R7945:Zgrf1
|
UTSW |
3 |
127,356,409 (GRCm39) |
missense |
probably benign |
0.37 |
|
R7996:Zgrf1
|
UTSW |
3 |
127,389,573 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R8165:Zgrf1
|
UTSW |
3 |
127,357,032 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R8198:Zgrf1
|
UTSW |
3 |
127,389,673 (GRCm39) |
critical splice donor site |
probably null |
|
|
R8296:Zgrf1
|
UTSW |
3 |
127,377,644 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8298:Zgrf1
|
UTSW |
3 |
127,408,878 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8341:Zgrf1
|
UTSW |
3 |
127,354,564 (GRCm39) |
nonsense |
probably null |
|
|
R8445:Zgrf1
|
UTSW |
3 |
127,379,854 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9088:Zgrf1
|
UTSW |
3 |
127,377,326 (GRCm39) |
missense |
probably benign |
0.21 |
|
R9236:Zgrf1
|
UTSW |
3 |
127,378,312 (GRCm39) |
missense |
probably benign |
0.09 |
|
R9250:Zgrf1
|
UTSW |
3 |
127,379,797 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9253:Zgrf1
|
UTSW |
3 |
127,392,428 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9464:Zgrf1
|
UTSW |
3 |
127,377,741 (GRCm39) |
missense |
probably benign |
0.03 |
|
R9680:Zgrf1
|
UTSW |
3 |
127,409,216 (GRCm39) |
missense |
probably benign |
0.38 |
|
RF015:Zgrf1
|
UTSW |
3 |
127,356,882 (GRCm39) |
missense |
probably benign |
0.02 |
|
| Predicted Primers |
|
| Posted On |
2022-10-06 |
Incidental Mutation