Incidental Mutation 'R4652:Prrc2c'
ID |
351350 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Prrc2c
|
Ensembl Gene |
ENSMUSG00000040225 |
Gene Name |
proline-rich coiled-coil 2C |
Synonyms |
9630039I18Rik, Bat2d, 1810043M20Rik, Bat2l2 |
MMRRC Submission |
041912-MU
|
Accession Numbers |
|
Essential gene? |
Possibly non essential
(E-score: 0.410)
|
Stock # |
R4652 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
162499354-162568125 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 162550843 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Histidine to Glutamine
at position 40
(H40Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000138609
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000028016]
[ENSMUST00000182149]
[ENSMUST00000182331]
[ENSMUST00000182593]
[ENSMUST00000182660]
[ENSMUST00000183011]
|
AlphaFold |
no structure available at present |
Predicted Effect |
unknown
Transcript: ENSMUST00000028016
AA Change: H40Q
|
SMART Domains |
Protein: ENSMUSP00000028016 Gene: ENSMUSG00000040225 AA Change: H40Q
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
164 |
7.7e-56 |
PFAM |
internal_repeat_2
|
167 |
349 |
4.39e-5 |
PROSPERO |
internal_repeat_1
|
336 |
391 |
2.14e-5 |
PROSPERO |
low complexity region
|
407 |
414 |
N/A |
INTRINSIC |
SCOP:d1eq1a_
|
447 |
591 |
2e-5 |
SMART |
low complexity region
|
649 |
669 |
N/A |
INTRINSIC |
low complexity region
|
733 |
745 |
N/A |
INTRINSIC |
coiled coil region
|
996 |
1026 |
N/A |
INTRINSIC |
low complexity region
|
1157 |
1186 |
N/A |
INTRINSIC |
low complexity region
|
1212 |
1222 |
N/A |
INTRINSIC |
internal_repeat_1
|
1240 |
1295 |
2.14e-5 |
PROSPERO |
low complexity region
|
1308 |
1335 |
N/A |
INTRINSIC |
low complexity region
|
1388 |
1409 |
N/A |
INTRINSIC |
low complexity region
|
1715 |
1746 |
N/A |
INTRINSIC |
low complexity region
|
1765 |
1803 |
N/A |
INTRINSIC |
low complexity region
|
1815 |
1832 |
N/A |
INTRINSIC |
low complexity region
|
1844 |
1909 |
N/A |
INTRINSIC |
internal_repeat_2
|
1962 |
2148 |
4.39e-5 |
PROSPERO |
low complexity region
|
2163 |
2177 |
N/A |
INTRINSIC |
low complexity region
|
2230 |
2252 |
N/A |
INTRINSIC |
low complexity region
|
2272 |
2286 |
N/A |
INTRINSIC |
low complexity region
|
2321 |
2338 |
N/A |
INTRINSIC |
low complexity region
|
2427 |
2438 |
N/A |
INTRINSIC |
low complexity region
|
2553 |
2576 |
N/A |
INTRINSIC |
low complexity region
|
2811 |
2828 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000182149
AA Change: H42Q
|
SMART Domains |
Protein: ENSMUSP00000138548 Gene: ENSMUSG00000040225 AA Change: H42Q
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
167 |
5.6e-73 |
PFAM |
internal_repeat_1
|
336 |
391 |
1.49e-5 |
PROSPERO |
low complexity region
|
407 |
414 |
N/A |
INTRINSIC |
SCOP:d1eq1a_
|
447 |
591 |
2e-5 |
SMART |
low complexity region
|
649 |
669 |
N/A |
INTRINSIC |
low complexity region
|
733 |
745 |
N/A |
INTRINSIC |
internal_repeat_3
|
754 |
925 |
9.16e-5 |
PROSPERO |
coiled coil region
|
996 |
1026 |
N/A |
INTRINSIC |
low complexity region
|
1157 |
1186 |
N/A |
INTRINSIC |
low complexity region
|
1212 |
1222 |
N/A |
INTRINSIC |
internal_repeat_1
|
1240 |
1295 |
1.49e-5 |
PROSPERO |
low complexity region
|
1308 |
1335 |
N/A |
INTRINSIC |
low complexity region
|
1388 |
1409 |
N/A |
INTRINSIC |
low complexity region
|
1715 |
1746 |
N/A |
INTRINSIC |
low complexity region
|
1765 |
1803 |
N/A |
INTRINSIC |
low complexity region
|
1815 |
1832 |
N/A |
INTRINSIC |
low complexity region
|
1844 |
1909 |
N/A |
INTRINSIC |
internal_repeat_2
|
1962 |
2148 |
3.08e-5 |
PROSPERO |
internal_repeat_3
|
1983 |
2153 |
9.16e-5 |
PROSPERO |
low complexity region
|
2163 |
2177 |
N/A |
INTRINSIC |
low complexity region
|
2230 |
2252 |
N/A |
INTRINSIC |
low complexity region
|
2272 |
2286 |
N/A |
INTRINSIC |
low complexity region
|
2321 |
2338 |
N/A |
INTRINSIC |
low complexity region
|
2427 |
2438 |
N/A |
INTRINSIC |
low complexity region
|
2553 |
2576 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182288
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000182308
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000182331
AA Change: H42Q
PolyPhen 2
Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
|
SMART Domains |
Protein: ENSMUSP00000138556 Gene: ENSMUSG00000040225 AA Change: H42Q
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
149 |
1e-68 |
PFAM |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000182593
AA Change: H40Q
|
SMART Domains |
Protein: ENSMUSP00000138674 Gene: ENSMUSG00000040225 AA Change: H40Q
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
165 |
4.1e-70 |
PFAM |
internal_repeat_1
|
334 |
389 |
9.57e-6 |
PROSPERO |
low complexity region
|
405 |
412 |
N/A |
INTRINSIC |
SCOP:d1eq1a_
|
445 |
589 |
3e-5 |
SMART |
low complexity region
|
647 |
667 |
N/A |
INTRINSIC |
low complexity region
|
731 |
743 |
N/A |
INTRINSIC |
internal_repeat_3
|
752 |
923 |
6.11e-5 |
PROSPERO |
coiled coil region
|
994 |
1024 |
N/A |
INTRINSIC |
low complexity region
|
1155 |
1184 |
N/A |
INTRINSIC |
low complexity region
|
1210 |
1220 |
N/A |
INTRINSIC |
internal_repeat_1
|
1238 |
1293 |
9.57e-6 |
PROSPERO |
low complexity region
|
1306 |
1333 |
N/A |
INTRINSIC |
low complexity region
|
1386 |
1407 |
N/A |
INTRINSIC |
low complexity region
|
1713 |
1744 |
N/A |
INTRINSIC |
low complexity region
|
1763 |
1801 |
N/A |
INTRINSIC |
low complexity region
|
1813 |
1830 |
N/A |
INTRINSIC |
low complexity region
|
1842 |
1907 |
N/A |
INTRINSIC |
internal_repeat_2
|
1960 |
2146 |
2.01e-5 |
PROSPERO |
internal_repeat_3
|
1981 |
2151 |
6.11e-5 |
PROSPERO |
low complexity region
|
2161 |
2175 |
N/A |
INTRINSIC |
low complexity region
|
2228 |
2250 |
N/A |
INTRINSIC |
low complexity region
|
2270 |
2284 |
N/A |
INTRINSIC |
low complexity region
|
2319 |
2336 |
N/A |
INTRINSIC |
low complexity region
|
2425 |
2436 |
N/A |
INTRINSIC |
low complexity region
|
2551 |
2574 |
N/A |
INTRINSIC |
low complexity region
|
2671 |
2682 |
N/A |
INTRINSIC |
low complexity region
|
2730 |
2747 |
N/A |
INTRINSIC |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000182660
AA Change: H42Q
|
SMART Domains |
Protein: ENSMUSP00000138433 Gene: ENSMUSG00000040225 AA Change: H42Q
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
167 |
7e-73 |
PFAM |
internal_repeat_1
|
336 |
391 |
2.14e-5 |
PROSPERO |
low complexity region
|
407 |
414 |
N/A |
INTRINSIC |
SCOP:d1eq1a_
|
447 |
591 |
2e-5 |
SMART |
low complexity region
|
649 |
669 |
N/A |
INTRINSIC |
low complexity region
|
733 |
745 |
N/A |
INTRINSIC |
coiled coil region
|
996 |
1026 |
N/A |
INTRINSIC |
low complexity region
|
1157 |
1186 |
N/A |
INTRINSIC |
low complexity region
|
1212 |
1222 |
N/A |
INTRINSIC |
internal_repeat_1
|
1240 |
1295 |
2.14e-5 |
PROSPERO |
low complexity region
|
1308 |
1335 |
N/A |
INTRINSIC |
low complexity region
|
1388 |
1409 |
N/A |
INTRINSIC |
low complexity region
|
1715 |
1746 |
N/A |
INTRINSIC |
low complexity region
|
1765 |
1803 |
N/A |
INTRINSIC |
low complexity region
|
1815 |
1832 |
N/A |
INTRINSIC |
low complexity region
|
1844 |
1909 |
N/A |
INTRINSIC |
internal_repeat_2
|
1962 |
2148 |
4.39e-5 |
PROSPERO |
low complexity region
|
2163 |
2177 |
N/A |
INTRINSIC |
low complexity region
|
2230 |
2252 |
N/A |
INTRINSIC |
low complexity region
|
2272 |
2286 |
N/A |
INTRINSIC |
low complexity region
|
2321 |
2338 |
N/A |
INTRINSIC |
low complexity region
|
2427 |
2438 |
N/A |
INTRINSIC |
low complexity region
|
2553 |
2576 |
N/A |
INTRINSIC |
low complexity region
|
2811 |
2828 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000183011
AA Change: H40Q
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000138609 Gene: ENSMUSG00000040225 AA Change: H40Q
Domain | Start | End | E-Value | Type |
Pfam:BAT2_N
|
1 |
160 |
3.2e-64 |
PFAM |
low complexity region
|
400 |
407 |
N/A |
INTRINSIC |
coiled coil region
|
443 |
560 |
N/A |
INTRINSIC |
|
Meta Mutation Damage Score |
0.6116 |
Coding Region Coverage |
- 1x: 99.3%
- 3x: 98.6%
- 10x: 97.4%
- 20x: 95.7%
|
Validation Efficiency |
95% (111/117) |
Allele List at MGI |
|
Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310022B05Rik |
T |
A |
8: 125,366,350 (GRCm39) |
Q131L |
probably damaging |
Het |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
4933409G03Rik |
G |
A |
2: 68,436,559 (GRCm39) |
E168K |
unknown |
Het |
A830018L16Rik |
C |
A |
1: 11,607,566 (GRCm39) |
|
probably benign |
Het |
Adam26b |
A |
G |
8: 43,974,375 (GRCm39) |
V209A |
possibly damaging |
Het |
Adh6a |
T |
A |
3: 138,031,876 (GRCm39) |
M256K |
probably benign |
Het |
Ahnak2 |
T |
G |
12: 112,741,271 (GRCm39) |
S128R |
possibly damaging |
Het |
Angptl2 |
G |
T |
2: 33,133,895 (GRCm39) |
D406Y |
probably damaging |
Het |
Ano10 |
A |
T |
9: 122,090,181 (GRCm39) |
Y377* |
probably null |
Het |
Arfgef1 |
C |
T |
1: 10,243,487 (GRCm39) |
D1021N |
probably damaging |
Het |
Arhgap17 |
G |
A |
7: 122,885,841 (GRCm39) |
|
probably benign |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Atp10b |
G |
A |
11: 43,085,472 (GRCm39) |
G284S |
probably damaging |
Het |
Atp13a4 |
A |
T |
16: 29,271,421 (GRCm39) |
D498E |
probably damaging |
Het |
C4a |
T |
A |
17: 35,029,108 (GRCm39) |
|
noncoding transcript |
Het |
Cacna1d |
C |
T |
14: 29,817,365 (GRCm39) |
M1232I |
probably benign |
Het |
Camsap3 |
A |
C |
8: 3,650,689 (GRCm39) |
K223T |
possibly damaging |
Het |
Cast |
A |
G |
13: 74,894,133 (GRCm39) |
S171P |
probably benign |
Het |
Cdh8 |
T |
A |
8: 99,751,491 (GRCm39) |
D742V |
probably benign |
Het |
Ceacam12 |
A |
G |
7: 17,801,359 (GRCm39) |
T113A |
probably damaging |
Het |
Cers3 |
G |
A |
7: 66,431,604 (GRCm39) |
|
probably null |
Het |
Cipc |
T |
C |
12: 87,008,864 (GRCm39) |
V241A |
probably benign |
Het |
Cntn5 |
C |
A |
9: 9,704,917 (GRCm39) |
K832N |
possibly damaging |
Het |
Col12a1 |
A |
T |
9: 79,520,228 (GRCm39) |
D2815E |
probably damaging |
Het |
Ctf2 |
T |
C |
7: 127,318,556 (GRCm39) |
T148A |
probably benign |
Het |
Cttnbp2 |
A |
G |
6: 18,434,037 (GRCm39) |
I607T |
possibly damaging |
Het |
Cux1 |
A |
T |
5: 136,596,083 (GRCm39) |
N4K |
probably damaging |
Het |
Dhx36 |
A |
T |
3: 62,408,419 (GRCm39) |
L140M |
probably benign |
Het |
Dhx58 |
T |
A |
11: 100,592,185 (GRCm39) |
N288Y |
probably damaging |
Het |
Dlgap1 |
T |
A |
17: 71,068,090 (GRCm39) |
Y554N |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,806,207 (GRCm39) |
Y127H |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,047,580 (GRCm39) |
M3140V |
probably benign |
Het |
Dnd1 |
G |
A |
18: 36,898,114 (GRCm39) |
|
probably benign |
Het |
Dpy19l1 |
A |
C |
9: 24,393,350 (GRCm39) |
S140A |
possibly damaging |
Het |
Dyrk1a |
C |
T |
16: 94,492,924 (GRCm39) |
T719I |
probably benign |
Het |
Erlin1 |
T |
A |
19: 44,029,231 (GRCm39) |
K234* |
probably null |
Het |
Fndc7 |
T |
C |
3: 108,770,135 (GRCm39) |
N597S |
probably benign |
Het |
Folh1 |
C |
A |
7: 86,393,633 (GRCm39) |
G360* |
probably null |
Het |
Frmd4b |
T |
C |
6: 97,272,716 (GRCm39) |
H846R |
probably benign |
Het |
Gm10375 |
C |
A |
14: 43,844,326 (GRCm39) |
|
probably null |
Het |
Gm27047 |
T |
C |
6: 130,607,479 (GRCm39) |
|
noncoding transcript |
Het |
Gm7168 |
A |
G |
17: 14,170,069 (GRCm39) |
R479G |
possibly damaging |
Het |
Gm9996 |
T |
A |
10: 29,019,754 (GRCm39) |
|
probably benign |
Het |
Gnat3 |
T |
A |
5: 18,220,568 (GRCm39) |
L247H |
probably damaging |
Het |
H2-D1 |
T |
G |
17: 35,485,492 (GRCm39) |
|
probably null |
Het |
Hpf1 |
T |
G |
8: 61,346,764 (GRCm39) |
S26R |
possibly damaging |
Het |
Ift80 |
T |
A |
3: 68,822,273 (GRCm39) |
N627I |
probably benign |
Het |
Inpp5d |
A |
G |
1: 87,593,173 (GRCm39) |
K91R |
probably benign |
Het |
Irgc |
C |
A |
7: 24,132,238 (GRCm39) |
R193L |
probably damaging |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lamc1 |
T |
G |
1: 153,104,523 (GRCm39) |
S59R |
probably damaging |
Het |
Lrrc9 |
T |
C |
12: 72,524,160 (GRCm39) |
W790R |
probably damaging |
Het |
Man1a2 |
A |
G |
3: 100,539,877 (GRCm39) |
L188P |
probably damaging |
Het |
Med8 |
A |
T |
4: 118,268,089 (GRCm39) |
E5V |
probably damaging |
Het |
Mefv |
A |
G |
16: 3,535,682 (GRCm39) |
L82P |
probably damaging |
Het |
Mettl25 |
A |
T |
10: 105,615,509 (GRCm39) |
C498* |
probably null |
Het |
Mettl3 |
T |
A |
14: 52,532,549 (GRCm39) |
I545F |
probably damaging |
Het |
Mvp |
T |
A |
7: 126,592,721 (GRCm39) |
I397F |
probably damaging |
Het |
Nlrp14 |
A |
T |
7: 106,781,024 (GRCm39) |
I74F |
probably benign |
Het |
Nudt5 |
G |
A |
2: 5,860,876 (GRCm39) |
|
probably benign |
Het |
Nyap2 |
T |
A |
1: 81,314,444 (GRCm39) |
D713E |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,929,703 (GRCm39) |
R5824C |
probably damaging |
Het |
Or4f6 |
G |
T |
2: 111,838,595 (GRCm39) |
S312Y |
probably damaging |
Het |
Or6c214 |
T |
C |
10: 129,591,287 (GRCm39) |
I11V |
probably benign |
Het |
Orc4 |
A |
T |
2: 48,826,762 (GRCm39) |
|
probably benign |
Het |
Pde10a |
T |
A |
17: 8,975,885 (GRCm39) |
N3K |
possibly damaging |
Het |
Pgm3 |
T |
A |
9: 86,440,523 (GRCm39) |
R389S |
probably benign |
Het |
Piwil4 |
G |
A |
9: 14,623,604 (GRCm39) |
R529* |
probably null |
Het |
Pkd2l2 |
A |
T |
18: 34,542,889 (GRCm39) |
R20* |
probably null |
Het |
Ppp4r3a |
T |
A |
12: 101,049,170 (GRCm39) |
|
probably benign |
Het |
Prkcq |
T |
C |
2: 11,284,333 (GRCm39) |
V501A |
possibly damaging |
Het |
Prkg1 |
T |
C |
19: 30,572,412 (GRCm39) |
T400A |
probably damaging |
Het |
Prps2 |
T |
C |
X: 166,135,288 (GRCm39) |
D183G |
probably damaging |
Het |
Ptcd1 |
A |
T |
5: 145,091,985 (GRCm39) |
H371Q |
probably benign |
Het |
Ptprk |
T |
C |
10: 28,139,686 (GRCm39) |
I137T |
probably damaging |
Het |
R3hdm1 |
T |
C |
1: 128,112,181 (GRCm39) |
S422P |
probably damaging |
Het |
Rapgef5 |
G |
A |
12: 117,677,863 (GRCm39) |
G366E |
probably damaging |
Het |
Rsf1 |
GCGGCGGCG |
GCGGCGGCGTCGGCGGCG |
7: 97,229,126 (GRCm39) |
|
probably benign |
Het |
Setd2 |
A |
G |
9: 110,423,200 (GRCm39) |
D2085G |
possibly damaging |
Het |
Sfxn3 |
A |
G |
19: 45,039,313 (GRCm39) |
|
probably null |
Het |
Sgce |
T |
C |
6: 4,689,560 (GRCm39) |
|
probably benign |
Het |
Sipa1l1 |
T |
A |
12: 82,469,245 (GRCm39) |
L1248* |
probably null |
Het |
Skint7 |
T |
G |
4: 111,839,309 (GRCm39) |
M201R |
probably damaging |
Het |
Slc18a1 |
A |
G |
8: 69,496,583 (GRCm39) |
M360T |
possibly damaging |
Het |
Srp68 |
A |
T |
11: 116,164,840 (GRCm39) |
S31R |
probably benign |
Het |
Stag1 |
T |
A |
9: 100,678,769 (GRCm39) |
M230K |
probably damaging |
Het |
Strc |
A |
T |
2: 121,204,829 (GRCm39) |
D985E |
possibly damaging |
Het |
Tars3 |
T |
A |
7: 65,339,717 (GRCm39) |
V704E |
probably damaging |
Het |
Tbc1d2b |
A |
G |
9: 90,089,940 (GRCm39) |
F863S |
probably damaging |
Het |
Tek |
T |
C |
4: 94,669,121 (GRCm39) |
S41P |
probably damaging |
Het |
Top1 |
T |
C |
2: 160,554,637 (GRCm39) |
Y463H |
probably damaging |
Het |
Trim24 |
T |
G |
6: 37,934,774 (GRCm39) |
|
probably null |
Het |
Ttn |
A |
G |
2: 76,576,979 (GRCm39) |
V24638A |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,701,213 (GRCm39) |
|
probably benign |
Het |
Txndc11 |
A |
G |
16: 10,892,986 (GRCm39) |
S915P |
probably benign |
Het |
Tyro3 |
G |
C |
2: 119,647,349 (GRCm39) |
G826A |
probably benign |
Het |
Ubxn4 |
T |
A |
1: 128,202,587 (GRCm39) |
W410R |
probably benign |
Het |
Vmn1r193 |
C |
T |
13: 22,403,695 (GRCm39) |
G99D |
probably damaging |
Het |
Vmn2r109 |
T |
A |
17: 20,761,656 (GRCm39) |
K567M |
probably damaging |
Het |
Vmn2r23 |
T |
C |
6: 123,718,689 (GRCm39) |
F681L |
probably damaging |
Het |
Vrk2 |
T |
C |
11: 26,439,803 (GRCm39) |
D256G |
probably damaging |
Het |
Vwa3a |
T |
A |
7: 120,378,138 (GRCm39) |
I476N |
probably damaging |
Het |
Wdr81 |
A |
G |
11: 75,342,066 (GRCm39) |
V1067A |
probably damaging |
Het |
Zcwpw2 |
A |
G |
9: 117,843,119 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Prrc2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00425:Prrc2c
|
APN |
1 |
162,548,182 (GRCm39) |
splice site |
probably null |
|
IGL00577:Prrc2c
|
APN |
1 |
162,525,685 (GRCm39) |
missense |
unknown |
|
IGL00580:Prrc2c
|
APN |
1 |
162,525,685 (GRCm39) |
missense |
unknown |
|
IGL01295:Prrc2c
|
APN |
1 |
162,510,061 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01554:Prrc2c
|
APN |
1 |
162,538,355 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01684:Prrc2c
|
APN |
1 |
162,534,031 (GRCm39) |
unclassified |
probably benign |
|
IGL01745:Prrc2c
|
APN |
1 |
162,552,297 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01770:Prrc2c
|
APN |
1 |
162,532,068 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01905:Prrc2c
|
APN |
1 |
162,532,898 (GRCm39) |
unclassified |
probably benign |
|
IGL02304:Prrc2c
|
APN |
1 |
162,511,705 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02389:Prrc2c
|
APN |
1 |
162,520,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02540:Prrc2c
|
APN |
1 |
162,550,706 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02681:Prrc2c
|
APN |
1 |
162,533,181 (GRCm39) |
unclassified |
probably benign |
|
IGL02686:Prrc2c
|
APN |
1 |
162,535,516 (GRCm39) |
unclassified |
probably benign |
|
IGL02795:Prrc2c
|
APN |
1 |
162,541,868 (GRCm39) |
missense |
probably benign |
|
IGL02894:Prrc2c
|
APN |
1 |
162,505,626 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02957:Prrc2c
|
APN |
1 |
162,534,104 (GRCm39) |
unclassified |
probably benign |
|
IGL02981:Prrc2c
|
APN |
1 |
162,532,748 (GRCm39) |
unclassified |
probably benign |
|
IGL03070:Prrc2c
|
APN |
1 |
162,504,978 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03096:Prrc2c
|
APN |
1 |
162,529,928 (GRCm39) |
missense |
unknown |
|
R0058:Prrc2c
|
UTSW |
1 |
162,526,453 (GRCm39) |
missense |
unknown |
|
R0058:Prrc2c
|
UTSW |
1 |
162,526,453 (GRCm39) |
missense |
unknown |
|
R0135:Prrc2c
|
UTSW |
1 |
162,543,052 (GRCm39) |
splice site |
probably benign |
|
R0279:Prrc2c
|
UTSW |
1 |
162,543,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R0363:Prrc2c
|
UTSW |
1 |
162,525,380 (GRCm39) |
missense |
unknown |
|
R0436:Prrc2c
|
UTSW |
1 |
162,532,883 (GRCm39) |
unclassified |
probably benign |
|
R0605:Prrc2c
|
UTSW |
1 |
162,509,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R0696:Prrc2c
|
UTSW |
1 |
162,536,421 (GRCm39) |
critical splice donor site |
probably null |
|
R0981:Prrc2c
|
UTSW |
1 |
162,533,550 (GRCm39) |
unclassified |
probably benign |
|
R1693:Prrc2c
|
UTSW |
1 |
162,546,282 (GRCm39) |
missense |
probably damaging |
0.98 |
R1714:Prrc2c
|
UTSW |
1 |
162,504,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R1791:Prrc2c
|
UTSW |
1 |
162,532,551 (GRCm39) |
unclassified |
probably benign |
|
R1794:Prrc2c
|
UTSW |
1 |
162,533,528 (GRCm39) |
unclassified |
probably benign |
|
R1998:Prrc2c
|
UTSW |
1 |
162,532,487 (GRCm39) |
unclassified |
probably benign |
|
R2040:Prrc2c
|
UTSW |
1 |
162,525,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R2168:Prrc2c
|
UTSW |
1 |
162,537,903 (GRCm39) |
unclassified |
probably benign |
|
R2246:Prrc2c
|
UTSW |
1 |
162,535,360 (GRCm39) |
unclassified |
probably benign |
|
R2830:Prrc2c
|
UTSW |
1 |
162,536,485 (GRCm39) |
unclassified |
probably benign |
|
R2926:Prrc2c
|
UTSW |
1 |
162,533,696 (GRCm39) |
unclassified |
probably benign |
|
R3703:Prrc2c
|
UTSW |
1 |
162,538,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R3745:Prrc2c
|
UTSW |
1 |
162,525,754 (GRCm39) |
missense |
unknown |
|
R3760:Prrc2c
|
UTSW |
1 |
162,520,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R3784:Prrc2c
|
UTSW |
1 |
162,537,238 (GRCm39) |
unclassified |
probably benign |
|
R3959:Prrc2c
|
UTSW |
1 |
162,536,461 (GRCm39) |
unclassified |
probably benign |
|
R4255:Prrc2c
|
UTSW |
1 |
162,533,895 (GRCm39) |
unclassified |
probably benign |
|
R4276:Prrc2c
|
UTSW |
1 |
162,501,160 (GRCm39) |
missense |
probably damaging |
1.00 |
R4421:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R4593:Prrc2c
|
UTSW |
1 |
162,525,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R4651:Prrc2c
|
UTSW |
1 |
162,550,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R4660:Prrc2c
|
UTSW |
1 |
162,508,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R4677:Prrc2c
|
UTSW |
1 |
162,532,748 (GRCm39) |
unclassified |
probably benign |
|
R4688:Prrc2c
|
UTSW |
1 |
162,525,256 (GRCm39) |
missense |
unknown |
|
R4753:Prrc2c
|
UTSW |
1 |
162,518,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Prrc2c
|
UTSW |
1 |
162,538,050 (GRCm39) |
missense |
unknown |
|
R4981:Prrc2c
|
UTSW |
1 |
162,520,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R4995:Prrc2c
|
UTSW |
1 |
162,532,879 (GRCm39) |
unclassified |
probably benign |
|
R5119:Prrc2c
|
UTSW |
1 |
162,533,009 (GRCm39) |
unclassified |
probably benign |
|
R5127:Prrc2c
|
UTSW |
1 |
162,525,415 (GRCm39) |
missense |
unknown |
|
R5291:Prrc2c
|
UTSW |
1 |
162,533,151 (GRCm39) |
unclassified |
probably benign |
|
R5474:Prrc2c
|
UTSW |
1 |
162,537,213 (GRCm39) |
unclassified |
probably benign |
|
R5543:Prrc2c
|
UTSW |
1 |
162,501,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R5579:Prrc2c
|
UTSW |
1 |
162,508,327 (GRCm39) |
critical splice donor site |
probably null |
|
R5594:Prrc2c
|
UTSW |
1 |
162,526,600 (GRCm39) |
missense |
unknown |
|
R5620:Prrc2c
|
UTSW |
1 |
162,501,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R5994:Prrc2c
|
UTSW |
1 |
162,501,725 (GRCm39) |
splice site |
probably null |
|
R6142:Prrc2c
|
UTSW |
1 |
162,537,956 (GRCm39) |
missense |
unknown |
|
R6199:Prrc2c
|
UTSW |
1 |
162,510,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R6277:Prrc2c
|
UTSW |
1 |
162,541,883 (GRCm39) |
missense |
probably benign |
|
R6504:Prrc2c
|
UTSW |
1 |
162,525,364 (GRCm39) |
missense |
unknown |
|
R6671:Prrc2c
|
UTSW |
1 |
162,525,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R6785:Prrc2c
|
UTSW |
1 |
162,536,670 (GRCm39) |
unclassified |
probably benign |
|
R6799:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6801:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6850:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6851:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6856:Prrc2c
|
UTSW |
1 |
162,509,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R6869:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6882:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6884:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R6897:Prrc2c
|
UTSW |
1 |
162,533,075 (GRCm39) |
unclassified |
probably benign |
|
R6934:Prrc2c
|
UTSW |
1 |
162,548,074 (GRCm39) |
missense |
probably benign |
0.10 |
R6976:Prrc2c
|
UTSW |
1 |
162,520,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R7132:Prrc2c
|
UTSW |
1 |
162,508,850 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7165:Prrc2c
|
UTSW |
1 |
162,501,086 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7282:Prrc2c
|
UTSW |
1 |
162,507,543 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7467:Prrc2c
|
UTSW |
1 |
162,504,932 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7915:Prrc2c
|
UTSW |
1 |
162,519,977 (GRCm39) |
missense |
probably benign |
0.39 |
R8068:Prrc2c
|
UTSW |
1 |
162,536,630 (GRCm39) |
unclassified |
probably benign |
|
R8529:Prrc2c
|
UTSW |
1 |
162,536,663 (GRCm39) |
unclassified |
probably benign |
|
R8734:Prrc2c
|
UTSW |
1 |
162,507,081 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8735:Prrc2c
|
UTSW |
1 |
162,537,127 (GRCm39) |
missense |
unknown |
|
R8813:Prrc2c
|
UTSW |
1 |
162,532,812 (GRCm39) |
missense |
unknown |
|
R8946:Prrc2c
|
UTSW |
1 |
162,536,478 (GRCm39) |
unclassified |
probably benign |
|
R8975:Prrc2c
|
UTSW |
1 |
162,533,630 (GRCm39) |
missense |
unknown |
|
R9035:Prrc2c
|
UTSW |
1 |
162,503,295 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9185:Prrc2c
|
UTSW |
1 |
162,532,212 (GRCm39) |
missense |
unknown |
|
R9261:Prrc2c
|
UTSW |
1 |
162,505,622 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9287:Prrc2c
|
UTSW |
1 |
162,541,843 (GRCm39) |
missense |
probably benign |
0.34 |
R9289:Prrc2c
|
UTSW |
1 |
162,507,130 (GRCm39) |
missense |
probably benign |
0.33 |
R9466:Prrc2c
|
UTSW |
1 |
162,503,258 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9523:Prrc2c
|
UTSW |
1 |
162,525,298 (GRCm39) |
missense |
unknown |
|
R9542:Prrc2c
|
UTSW |
1 |
162,508,359 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9629:Prrc2c
|
UTSW |
1 |
162,519,959 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9744:Prrc2c
|
UTSW |
1 |
162,505,733 (GRCm39) |
missense |
possibly damaging |
0.96 |
R9748:Prrc2c
|
UTSW |
1 |
162,535,435 (GRCm39) |
missense |
unknown |
|
X0020:Prrc2c
|
UTSW |
1 |
162,535,416 (GRCm39) |
unclassified |
probably benign |
|
X0039:Prrc2c
|
UTSW |
1 |
162,532,362 (GRCm39) |
frame shift |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- GGCAGTTTCCTACAATGAGAGAAG -3'
(R):5'- TTTGCTGGGGTCCCAAGATG -3'
Sequencing Primer
(F):5'- AACAGATTCTGACTCACTTTTCTTC -3'
(R):5'- GGTCCCAAGATGGCTTAATATTTTG -3'
|
Posted On |
2015-10-08 |