Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5430401F13Rik |
AGGAAAAGGTGGCCAG |
AGGAAAAGGTGGCCAGCAAAAACAGAAAGGAAAAGGTGGCCAG |
6: 131,529,851 (GRCm39) |
|
probably benign |
Het |
5430401F13Rik |
AAGGAAAAGGTGGCCAG |
AAGGAAAAGGTGGCCAGCAAAAACAGAAAGGAAAAGGTGGCCAG |
6: 131,529,850 (GRCm39) |
|
probably benign |
Het |
Abcf1 |
TGTC |
T |
17: 36,274,080 (GRCm39) |
|
probably benign |
Het |
Ankrd24 |
GAGG |
GAGGCAGAGGCTTAGG |
10: 81,479,407 (GRCm39) |
|
probably null |
Het |
Ckap2l |
TGCA |
T |
2: 129,112,569 (GRCm39) |
|
probably benign |
Het |
Cox7a2l |
GGA |
GGAGGGGGA |
17: 83,810,151 (GRCm39) |
|
probably benign |
Het |
Cpne1 |
TCCAC |
TC |
2: 155,915,430 (GRCm39) |
|
probably benign |
Het |
Ehbp1 |
ACTG |
A |
11: 21,956,783 (GRCm39) |
|
probably benign |
Het |
Eml6 |
TCCTAAAAAAACAAAAC |
TC |
11: 29,702,549 (GRCm39) |
|
probably benign |
Het |
Fbrsl1 |
G |
GCGTGTGCTAGTA |
5: 110,526,017 (GRCm39) |
|
probably null |
Het |
Gabre |
CTC |
CTCCGGGTC |
X: 71,313,667 (GRCm39) |
|
probably benign |
Het |
Gm8369 |
GTG |
GTGGGTATG |
19: 11,489,146 (GRCm39) |
|
probably benign |
Het |
Igf1r |
GGAGATGGAGC |
GGAGATGGAGCTTGAGATGGAGC |
7: 67,875,924 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
ACAG |
ACAGCCCCAG |
1: 83,019,866 (GRCm39) |
|
probably benign |
Het |
Krtap28-10 |
ACAGC |
ACAGCCACAGCCACCCCAGC |
1: 83,020,007 (GRCm39) |
|
probably benign |
Het |
Lce1m |
C |
CCGCTGCTGCCAT |
3: 92,925,607 (GRCm39) |
|
probably benign |
Het |
Lrch1 |
CGTGGTGCTGGTGGTGTTGGTGGTGTTGGTGGTGCTGGTGG |
CGTGGTGTTGGTGGTGTTGGTGGTGCTGGTGG |
14: 75,184,989 (GRCm39) |
|
probably benign |
Het |
Map1a |
AGCTCCAGCTCCAGCTCCAGCTCCA |
AGCTCCAGCTCCAGCTCCAGCTCCAGCTCCGGCTCCAGCTCCAGCTCCAGCTCCA |
2: 121,136,775 (GRCm39) |
|
probably benign |
Het |
Mast4 |
CCTCGGGGACAAGCTGTGAGTTGGGGAAC |
CC |
13: 102,875,749 (GRCm39) |
|
probably benign |
Het |
Med12l |
GCAACA |
GCAACAACA |
3: 59,183,377 (GRCm39) |
|
probably benign |
Het |
Nefh |
TGGGGACTTGG |
TGGGGACTTGGACTCCCCGGGGGACTTGG |
11: 4,891,046 (GRCm39) |
|
probably benign |
Het |
Nefh |
TTGGCCTCAGCTGGGGACTTGGCCTCA |
TTGGCCTCAGCTGGAGACTTGGCCTCAGCTGGGGACTTGGCCTCA |
11: 4,890,999 (GRCm39) |
|
probably benign |
Het |
Nefh |
TGGC |
TGGCGTCACCTGGGGACTGGGC |
11: 4,891,054 (GRCm39) |
|
probably benign |
Het |
Nusap1 |
AGCAGTGAGGAGCAAGCTGAGA |
AGCAGTGAGGAGCAAGCTGAGATACACGTTCGCAGTGAGGAGCAAGCTGAGA |
2: 119,458,070 (GRCm39) |
|
probably benign |
Het |
Or4k41 |
G |
A |
2: 111,279,896 (GRCm39) |
G137D |
not run |
Het |
Ren1 |
ACCGC |
AC |
1: 133,278,519 (GRCm39) |
|
probably benign |
Het |
Sbp |
AAGATG |
AAGATGCTGACAACAGAGATG |
17: 24,164,358 (GRCm39) |
|
probably benign |
Het |
Sbp |
ATG |
ATGCTGACAACAAAGCTG |
17: 24,164,361 (GRCm39) |
|
probably benign |
Het |
Six5 |
CGGA |
C |
7: 18,828,725 (GRCm39) |
|
probably benign |
Het |
Spmap2l |
CAAGGCCAG |
CAAGGCCAGCGATCCTCCCCAGTCCCGAAAGGCCAG |
5: 77,164,268 (GRCm39) |
|
probably benign |
Het |
Tgoln1 |
TGGGCTTG |
TGGGCTTGTCAGAATCACCTCCTGGGGGCTTG |
6: 72,593,019 (GRCm39) |
|
probably benign |
Het |
Ufl1 |
C |
T |
4: 25,280,628 (GRCm39) |
R73Q |
possibly damaging |
Het |
Zfhx3 |
CAGCAGCA |
CAGCAGCAATAGCAGCA |
8: 109,682,730 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Dnmt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Dnmt1
|
APN |
9 |
20,821,566 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01093:Dnmt1
|
APN |
9 |
20,821,081 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01160:Dnmt1
|
APN |
9 |
20,828,615 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01704:Dnmt1
|
APN |
9 |
20,821,476 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02105:Dnmt1
|
APN |
9 |
20,819,178 (GRCm39) |
missense |
unknown |
|
IGL02124:Dnmt1
|
APN |
9 |
20,819,845 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02188:Dnmt1
|
APN |
9 |
20,853,034 (GRCm39) |
nonsense |
probably null |
|
IGL02409:Dnmt1
|
APN |
9 |
20,837,793 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02579:Dnmt1
|
APN |
9 |
20,829,416 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02625:Dnmt1
|
APN |
9 |
20,838,442 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02794:Dnmt1
|
APN |
9 |
20,847,847 (GRCm39) |
missense |
probably benign |
|
IGL02795:Dnmt1
|
APN |
9 |
20,838,407 (GRCm39) |
missense |
probably benign |
0.12 |
IGL02938:Dnmt1
|
APN |
9 |
20,852,669 (GRCm39) |
missense |
probably benign |
0.23 |
IGL03245:Dnmt1
|
APN |
9 |
20,827,056 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03303:Dnmt1
|
APN |
9 |
20,838,006 (GRCm39) |
missense |
probably benign |
|
Blankslate
|
UTSW |
9 |
20,823,521 (GRCm39) |
missense |
possibly damaging |
0.86 |
Midrash
|
UTSW |
9 |
20,821,089 (GRCm39) |
nonsense |
probably null |
|
Rashi
|
UTSW |
9 |
20,833,408 (GRCm39) |
missense |
possibly damaging |
0.94 |
B5639:Dnmt1
|
UTSW |
9 |
20,819,264 (GRCm39) |
splice site |
probably benign |
|
BB003:Dnmt1
|
UTSW |
9 |
20,818,855 (GRCm39) |
missense |
unknown |
|
BB013:Dnmt1
|
UTSW |
9 |
20,818,855 (GRCm39) |
missense |
unknown |
|
PIT4576001:Dnmt1
|
UTSW |
9 |
20,823,071 (GRCm39) |
missense |
probably benign |
0.28 |
R0071:Dnmt1
|
UTSW |
9 |
20,819,916 (GRCm39) |
missense |
probably damaging |
0.99 |
R0180:Dnmt1
|
UTSW |
9 |
20,819,916 (GRCm39) |
missense |
probably damaging |
0.99 |
R0368:Dnmt1
|
UTSW |
9 |
20,853,053 (GRCm39) |
missense |
probably damaging |
0.99 |
R0387:Dnmt1
|
UTSW |
9 |
20,829,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R0529:Dnmt1
|
UTSW |
9 |
20,822,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R0532:Dnmt1
|
UTSW |
9 |
20,829,852 (GRCm39) |
splice site |
probably benign |
|
R0612:Dnmt1
|
UTSW |
9 |
20,829,489 (GRCm39) |
missense |
probably damaging |
0.98 |
R1109:Dnmt1
|
UTSW |
9 |
20,833,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R1298:Dnmt1
|
UTSW |
9 |
20,852,752 (GRCm39) |
missense |
probably benign |
|
R1345:Dnmt1
|
UTSW |
9 |
20,819,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R1472:Dnmt1
|
UTSW |
9 |
20,843,472 (GRCm39) |
missense |
probably benign |
0.28 |
R1654:Dnmt1
|
UTSW |
9 |
20,847,870 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1817:Dnmt1
|
UTSW |
9 |
20,838,422 (GRCm39) |
missense |
probably benign |
|
R1836:Dnmt1
|
UTSW |
9 |
20,829,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R1957:Dnmt1
|
UTSW |
9 |
20,838,442 (GRCm39) |
missense |
probably benign |
0.01 |
R1958:Dnmt1
|
UTSW |
9 |
20,838,442 (GRCm39) |
missense |
probably benign |
0.01 |
R2097:Dnmt1
|
UTSW |
9 |
20,821,084 (GRCm39) |
missense |
probably benign |
0.00 |
R2145:Dnmt1
|
UTSW |
9 |
20,848,451 (GRCm39) |
splice site |
probably benign |
|
R2326:Dnmt1
|
UTSW |
9 |
20,835,442 (GRCm39) |
splice site |
probably benign |
|
R4199:Dnmt1
|
UTSW |
9 |
20,849,414 (GRCm39) |
missense |
probably benign |
0.00 |
R4456:Dnmt1
|
UTSW |
9 |
20,821,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R4518:Dnmt1
|
UTSW |
9 |
20,823,274 (GRCm39) |
missense |
probably benign |
0.00 |
R4586:Dnmt1
|
UTSW |
9 |
20,837,989 (GRCm39) |
missense |
probably benign |
0.05 |
R4836:Dnmt1
|
UTSW |
9 |
20,819,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R5014:Dnmt1
|
UTSW |
9 |
20,823,550 (GRCm39) |
missense |
probably benign |
0.07 |
R5338:Dnmt1
|
UTSW |
9 |
20,864,015 (GRCm39) |
missense |
probably benign |
0.44 |
R5385:Dnmt1
|
UTSW |
9 |
20,829,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R5579:Dnmt1
|
UTSW |
9 |
20,831,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5645:Dnmt1
|
UTSW |
9 |
20,833,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R5719:Dnmt1
|
UTSW |
9 |
20,823,891 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5881:Dnmt1
|
UTSW |
9 |
20,864,013 (GRCm39) |
missense |
probably damaging |
0.97 |
R6039:Dnmt1
|
UTSW |
9 |
20,837,716 (GRCm39) |
intron |
probably benign |
|
R6039:Dnmt1
|
UTSW |
9 |
20,837,716 (GRCm39) |
intron |
probably benign |
|
R6143:Dnmt1
|
UTSW |
9 |
20,838,430 (GRCm39) |
missense |
probably benign |
0.30 |
R6342:Dnmt1
|
UTSW |
9 |
20,821,089 (GRCm39) |
nonsense |
probably null |
|
R6374:Dnmt1
|
UTSW |
9 |
20,835,341 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6953:Dnmt1
|
UTSW |
9 |
20,829,822 (GRCm39) |
missense |
probably benign |
|
R6990:Dnmt1
|
UTSW |
9 |
20,827,110 (GRCm39) |
nonsense |
probably null |
|
R7089:Dnmt1
|
UTSW |
9 |
20,819,785 (GRCm39) |
missense |
probably damaging |
0.99 |
R7463:Dnmt1
|
UTSW |
9 |
20,823,521 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7522:Dnmt1
|
UTSW |
9 |
20,831,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R7695:Dnmt1
|
UTSW |
9 |
20,825,281 (GRCm39) |
missense |
probably null |
1.00 |
R7785:Dnmt1
|
UTSW |
9 |
20,833,345 (GRCm39) |
missense |
probably damaging |
0.98 |
R7926:Dnmt1
|
UTSW |
9 |
20,818,855 (GRCm39) |
missense |
unknown |
|
R8037:Dnmt1
|
UTSW |
9 |
20,852,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R8038:Dnmt1
|
UTSW |
9 |
20,852,860 (GRCm39) |
missense |
probably damaging |
0.99 |
R8424:Dnmt1
|
UTSW |
9 |
20,829,836 (GRCm39) |
missense |
probably benign |
0.07 |
R8692:Dnmt1
|
UTSW |
9 |
20,853,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R9016:Dnmt1
|
UTSW |
9 |
20,847,855 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9101:Dnmt1
|
UTSW |
9 |
20,852,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R9200:Dnmt1
|
UTSW |
9 |
20,819,896 (GRCm39) |
missense |
probably benign |
0.00 |
R9248:Dnmt1
|
UTSW |
9 |
20,833,408 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9317:Dnmt1
|
UTSW |
9 |
20,829,575 (GRCm39) |
missense |
probably damaging |
0.99 |
R9352:Dnmt1
|
UTSW |
9 |
20,840,384 (GRCm39) |
missense |
probably benign |
0.00 |
R9438:Dnmt1
|
UTSW |
9 |
20,827,190 (GRCm39) |
missense |
probably benign |
|
RF003:Dnmt1
|
UTSW |
9 |
20,821,427 (GRCm39) |
nonsense |
probably null |
|
RF004:Dnmt1
|
UTSW |
9 |
20,821,423 (GRCm39) |
nonsense |
probably null |
|
RF011:Dnmt1
|
UTSW |
9 |
20,821,440 (GRCm39) |
nonsense |
probably null |
|
RF011:Dnmt1
|
UTSW |
9 |
20,821,424 (GRCm39) |
nonsense |
probably null |
|
RF015:Dnmt1
|
UTSW |
9 |
20,821,425 (GRCm39) |
nonsense |
probably null |
|
RF015:Dnmt1
|
UTSW |
9 |
20,821,420 (GRCm39) |
nonsense |
probably null |
|
RF017:Dnmt1
|
UTSW |
9 |
20,821,422 (GRCm39) |
nonsense |
probably null |
|
RF023:Dnmt1
|
UTSW |
9 |
20,821,427 (GRCm39) |
nonsense |
probably null |
|
RF024:Dnmt1
|
UTSW |
9 |
20,821,434 (GRCm39) |
small insertion |
probably benign |
|
RF024:Dnmt1
|
UTSW |
9 |
20,821,426 (GRCm39) |
nonsense |
probably null |
|
RF025:Dnmt1
|
UTSW |
9 |
20,821,431 (GRCm39) |
nonsense |
probably null |
|
RF025:Dnmt1
|
UTSW |
9 |
20,821,416 (GRCm39) |
nonsense |
probably null |
|
RF029:Dnmt1
|
UTSW |
9 |
20,821,419 (GRCm39) |
nonsense |
probably null |
|
RF034:Dnmt1
|
UTSW |
9 |
20,821,416 (GRCm39) |
nonsense |
probably null |
|
RF037:Dnmt1
|
UTSW |
9 |
20,821,429 (GRCm39) |
nonsense |
probably null |
|
RF037:Dnmt1
|
UTSW |
9 |
20,821,415 (GRCm39) |
critical splice donor site |
probably benign |
|
RF042:Dnmt1
|
UTSW |
9 |
20,821,415 (GRCm39) |
nonsense |
probably null |
|
RF045:Dnmt1
|
UTSW |
9 |
20,821,433 (GRCm39) |
small insertion |
probably benign |
|
RF045:Dnmt1
|
UTSW |
9 |
20,821,425 (GRCm39) |
nonsense |
probably null |
|
RF047:Dnmt1
|
UTSW |
9 |
20,821,421 (GRCm39) |
nonsense |
probably null |
|
RF048:Dnmt1
|
UTSW |
9 |
20,821,422 (GRCm39) |
nonsense |
probably null |
|
RF054:Dnmt1
|
UTSW |
9 |
20,821,435 (GRCm39) |
nonsense |
probably null |
|
RF055:Dnmt1
|
UTSW |
9 |
20,821,432 (GRCm39) |
small insertion |
probably benign |
|
RF055:Dnmt1
|
UTSW |
9 |
20,821,431 (GRCm39) |
nonsense |
probably null |
|
RF055:Dnmt1
|
UTSW |
9 |
20,821,424 (GRCm39) |
nonsense |
probably null |
|
RF059:Dnmt1
|
UTSW |
9 |
20,821,434 (GRCm39) |
small insertion |
probably benign |
|
RF059:Dnmt1
|
UTSW |
9 |
20,821,435 (GRCm39) |
nonsense |
probably null |
|
RF060:Dnmt1
|
UTSW |
9 |
20,821,438 (GRCm39) |
nonsense |
probably null |
|
RF061:Dnmt1
|
UTSW |
9 |
20,821,426 (GRCm39) |
nonsense |
probably null |
|
X0026:Dnmt1
|
UTSW |
9 |
20,825,210 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Dnmt1
|
UTSW |
9 |
20,837,850 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Dnmt1
|
UTSW |
9 |
20,827,159 (GRCm39) |
missense |
probably damaging |
0.99 |
|