Other mutations in this stock |
Total: 221 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001K19Rik |
TTC |
TTCATC |
12: 110,668,447 |
|
probably benign |
Het |
1700001K19Rik |
TTC |
TTCGTC |
12: 110,668,450 |
|
probably benign |
Het |
2010300C02Rik |
T |
A |
1: 37,625,035 |
E594V |
probably benign |
Homo |
2010300C02Rik |
C |
A |
1: 37,625,036 |
E594* |
probably null |
Homo |
2010300C02Rik |
A |
G |
1: 37,625,102 |
S47P |
probably damaging |
Homo |
4930402H24Rik |
TCC |
TCCCCC |
2: 130,770,739 |
|
probably benign |
Het |
4930402H24Rik |
TCC |
TCCACC |
2: 130,770,742 |
|
probably benign |
Het |
4930402H24Rik |
C |
CTCG |
2: 130,770,753 |
|
probably benign |
Het |
Abt1 |
TTCTTGCT |
TT |
13: 23,423,711 |
|
probably benign |
Het |
AI837181 |
GGC |
GGCCGC |
19: 5,425,229 |
|
probably benign |
Het |
Akap12 |
AAA |
AAACAA |
10: 4,353,837 |
|
probably benign |
Het |
Alg1 |
GCTCACTCAC |
GCTCAC |
16: 5,244,561 |
|
probably null |
Homo |
Alg9 |
G |
GCGA |
9: 50,775,431 |
|
probably benign |
Het |
Amfr |
GCC |
GCCGGCGCGAGCTCC |
8: 94,012,292 |
|
probably benign |
Het |
Anapc2 |
TGGCGGTGGCGGCGGCGGCGGCGGCGGCGG |
TGGCGGCGGCGGCGGCGG |
2: 25,272,532 |
|
probably benign |
Het |
Anxa7 |
C |
T |
14: 20,469,411 |
G113E |
probably damaging |
Homo |
Apc |
CCAATAAAG |
CCAATAAAGTCAATAAAG |
18: 34,281,998 |
|
probably benign |
Het |
Apc |
AATAAAGC |
AATAAAGCCTATAAAGC |
18: 34,282,000 |
|
probably benign |
Het |
Apc |
AAGC |
AAGCCAATATAGC |
18: 34,282,004 |
|
probably null |
Het |
Atad3a |
C |
A |
4: 155,753,939 |
R207L |
probably damaging |
Homo |
BC051142 |
AGC |
AGCGGC |
17: 34,460,058 |
|
probably benign |
Het |
BC051142 |
AGC |
AGCGGC |
17: 34,460,061 |
|
probably benign |
Het |
Blm |
ACCT |
ACCTCCCT |
7: 80,463,767 |
|
probably benign |
Homo |
Blm |
TCCTCCTCCTCCTCCTCCTCCTCC |
TCCTCCTCCTCCACCTCCTCCTCCTCCTCCTCCTCC |
7: 80,512,907 |
|
probably benign |
Het |
Bmp5 |
GAGGAGT |
G |
9: 75,776,375 |
|
probably benign |
Homo |
Bpifa6 |
A |
T |
2: 153,986,376 |
Q134L |
probably benign |
Homo |
Bpifa6 |
A |
T |
2: 153,986,398 |
R141S |
probably benign |
Homo |
Btnl10 |
AGA |
AGAGGA |
11: 58,923,929 |
|
probably benign |
Homo |
Cacna1a |
ACC |
ACCGCC |
8: 84,638,717 |
|
probably benign |
Het |
Cacna1a |
ACC |
ACCTCC |
8: 84,638,726 |
|
probably benign |
Het |
Calhm1 |
TGGCTGTGGCTG |
TGGCTGTGGCTGCGGCTGTGGCTG |
19: 47,141,262 |
|
probably benign |
Het |
Catsper2 |
C |
CTTTTACTTTTTT |
2: 121,397,542 |
|
probably benign |
Homo |
Catsper2 |
TGTC |
TGTCGTC |
2: 121,397,779 |
|
probably benign |
Homo |
Catsper2 |
CAT |
CATTAT |
2: 121,397,782 |
|
probably benign |
Het |
Catsper2 |
ATCGTCGTCGTC |
ATCGTCGTCGTCGTC |
2: 121,397,795 |
|
probably benign |
Het |
Ccdc170 |
ACCGCC |
ACCGCCGCC |
10: 4,561,008 |
|
probably benign |
Het |
Ccdc170 |
ACC |
ACCGCC |
10: 4,561,023 |
|
probably benign |
Het |
Ccdc170 |
AC |
ACCTC |
10: 4,561,029 |
|
probably benign |
Het |
Ccnk |
TTCCCAC |
T |
12: 108,202,507 |
|
probably benign |
Het |
Cdx1 |
GGGCTGC |
GGGCTGCGGCTGC |
18: 61,019,867 |
|
probably benign |
Het |
Cdx1 |
GCTGCT |
GCTGCTTCTGCT |
18: 61,019,869 |
|
probably benign |
Het |
Cep112 |
G |
GCTCT |
11: 108,425,352 |
|
probably benign |
Het |
Cep89 |
GACT |
G |
7: 35,409,641 |
|
probably benign |
Het |
Cfap46 |
CCTTCT |
CCTTCTTCT |
7: 139,638,930 |
|
probably benign |
Homo |
Chd4 |
GC |
GCTCCCTC |
6: 125,122,131 |
|
probably benign |
Homo |
Cluh |
GCCTGA |
GCCTGAACCTGA |
11: 74,669,520 |
|
probably benign |
Het |
Cnpy3 |
CCT |
CCTACT |
17: 46,736,747 |
|
probably null |
Het |
Cntnap1 |
A |
ACCCCCC |
11: 101,189,569 |
|
probably benign |
Het |
Cntnap1 |
CCCAGC |
CCCAGCACCAGC |
11: 101,189,572 |
|
probably benign |
Het |
Cntnap1 |
CCAGCC |
CCAGCCTCAGCC |
11: 101,189,585 |
|
probably benign |
Het |
Cntnap1 |
GCCCCA |
GCCCCACCCCCA |
11: 101,189,588 |
|
probably benign |
Het |
Col4a3 |
CGTTTTTTTTTTTTTTTT |
C |
1: 82,718,906 |
|
probably null |
Het |
Cpne1 |
AGA |
AGAGAGA |
2: 156,072,025 |
|
probably null |
Homo |
Ctsm |
AGTG |
AGTGGGTG |
13: 61,537,836 |
|
probably null |
Homo |
Cttnbp2 |
GCTGCT |
GCTGCTCCTGCT |
6: 18,367,461 |
|
probably benign |
Het |
Cttnbp2 |
GCTGCT |
GCTGCTTCTGCT |
6: 18,367,467 |
|
probably benign |
Het |
Cul9 |
CTTC |
CTTCTTC |
17: 46,500,848 |
|
probably benign |
Het |
Cul9 |
TCC |
TCCGCC |
17: 46,500,850 |
|
probably benign |
Het |
Cul9 |
TCC |
TCCCCC |
17: 46,500,853 |
|
probably benign |
Het |
Cul9 |
TCC |
TCCCCC |
17: 46,500,856 |
|
probably benign |
Het |
Cybrd1 |
GAAT |
G |
2: 71,138,511 |
|
probably benign |
Homo |
Dbr1 |
AGGAGG |
AGGAGGCGGAGG |
9: 99,583,689 |
|
probably benign |
Het |
Dbr1 |
AGGAGG |
AGGAGGCGGAGG |
9: 99,583,692 |
|
probably benign |
Het |
Dbr1 |
AGG |
AGGAGGCGG |
9: 99,583,701 |
|
probably benign |
Het |
Dbr1 |
GG |
GGAGGAAG |
9: 99,583,702 |
|
probably benign |
Het |
Dcaf8 |
C |
T |
1: 172,172,856 |
H194Y |
probably damaging |
Homo |
Dnajc19 |
AC |
ACGC |
3: 34,057,994 |
|
probably null |
Het |
Dthd1 |
GAC |
GACTAC |
5: 62,843,024 |
|
probably benign |
Homo |
Dusp10 |
G |
T |
1: 184,037,056 |
C73F |
probably damaging |
Homo |
Eif3a |
A |
ATTTTT |
19: 60,775,291 |
|
probably benign |
Homo |
Ermn |
CTT |
CTTGTT |
2: 58,048,080 |
|
probably benign |
Het |
Ermn |
TC |
TCTAC |
2: 58,048,088 |
|
probably benign |
Het |
Fam45a |
ACTC |
ACTCCTC |
19: 60,814,618 |
|
probably benign |
Homo |
Fam45a |
T |
TTCA |
19: 60,814,622 |
|
probably benign |
Homo |
Fbxo38 |
TGCAGC |
TGC |
18: 62,515,347 |
|
probably benign |
Het |
Frem3 |
CT |
CTTGT |
8: 80,615,241 |
|
probably benign |
Homo |
Gabre |
AGGCT |
AGGCTGCGGCT |
X: 72,270,418 |
|
probably benign |
Homo |
Gabre |
T |
TGAGGCC |
X: 72,270,422 |
|
probably benign |
Homo |
Gm10800 |
A |
AC |
2: 98,667,033 |
|
probably null |
Homo |
Gm14393 |
T |
G |
2: 175,061,820 |
N98T |
probably benign |
Het |
Gm16503 |
G |
A |
4: 147,541,253 |
G68E |
unknown |
Het |
Gm28040 |
TG |
TGGCACCTTTCGAG |
1: 133,327,323 |
|
probably benign |
Homo |
Gm4340 |
AGC |
AGCCGC |
10: 104,196,079 |
|
probably benign |
Het |
Gm6309 |
C |
T |
5: 146,168,183 |
V307I |
probably benign |
Het |
Gm7534 |
TG |
TGCCG |
4: 134,202,630 |
|
probably benign |
Homo |
Golga5 |
G |
A |
12: 102,475,660 |
|
probably null |
Homo |
Gpatch11 |
GAAGAG |
GAAGAGCAAGAG |
17: 78,842,170 |
|
probably benign |
Het |
Gpatch11 |
AAGAGG |
AAGAGGCAGAGG |
17: 78,842,171 |
|
probably benign |
Het |
Gpatch11 |
AGAGGA |
AGAGGATGAGGA |
17: 78,842,172 |
|
probably benign |
Het |
Gpatch11 |
GAGGAA |
GAGGAATAGGAA |
17: 78,842,173 |
|
probably null |
Het |
Gpatch11 |
AGGAA |
AGGAAGTGGAA |
17: 78,842,180 |
|
probably benign |
Het |
H2-K1 |
GTTT |
G |
17: 33,997,042 |
|
probably benign |
Homo |
Hcn1 |
GCAGC |
GCAGCGACAGC |
13: 117,975,808 |
|
probably benign |
Homo |
Hoxa10 |
T |
A |
6: 52,234,186 |
Q250L |
possibly damaging |
Homo |
Igf1r |
TGGAGC |
TGGAGCTGGAGAGGGAGC |
7: 68,226,181 |
|
probably benign |
Het |
Igf1r |
C |
CTGGAGATGGAGA |
7: 68,226,186 |
|
probably benign |
Het |
Il17rd |
CGG |
CGGTGG |
14: 27,082,677 |
|
probably benign |
Het |
Il2 |
GG |
GGGGCTTGAAGTAG |
3: 37,125,829 |
|
probably benign |
Het |
Ipo9 |
TCC |
TCCCCC |
1: 135,386,281 |
|
probably benign |
Het |
Iqcc |
T |
TGTCAGCCTCCTTGTACCC |
4: 129,616,676 |
|
probably benign |
Het |
Isg20l2 |
AAG |
AAGTAG |
3: 87,931,715 |
|
probably null |
Het |
Kcng4 |
G |
T |
8: 119,633,519 |
Y39* |
probably null |
Homo |
Kmt2b |
TCCTCC |
TCCTCCCCCTCC |
7: 30,586,360 |
|
probably benign |
Het |
Kmt2b |
CTCCTC |
CTCCTCGTCCTC |
7: 30,586,362 |
|
probably benign |
Het |
Kmt2b |
CCTCCT |
CCTCCTACTCCT |
7: 30,586,364 |
|
probably null |
Het |
Kmt2b |
TCCTCC |
TCCTCCACCTCC |
7: 30,586,366 |
|
probably benign |
Het |
Kmt2b |
CCTCCT |
CCTCCTGCTCCT |
7: 30,586,373 |
|
probably benign |
Het |
Kmt2c |
TGCTGCTGCTGTTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT |
TGCTGCTGCTGCTGCTGTTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCT |
5: 25,315,763 |
|
probably benign |
Homo |
Krtap9-3 |
AC |
ACAGGTGCCTC |
11: 99,598,004 |
|
probably benign |
Homo |
Las1l |
AGG |
AGGGGG |
X: 95,940,827 |
|
probably benign |
Het |
Las1l |
GA |
GAGAA |
X: 95,940,832 |
|
probably benign |
Het |
Las1l |
A |
AGGC |
X: 95,940,833 |
|
probably benign |
Het |
Lce1m |
TGCCAC |
TGCCACTGCTGCAGCCAC |
3: 93,018,148 |
|
probably benign |
Het |
Leo1 |
GGTACCATGCAG |
GG |
9: 75,450,572 |
|
probably benign |
Het |
Lrit3 |
CATA |
CATAAATA |
3: 129,803,910 |
|
probably benign |
Homo |
Lrmp |
CACATTG |
CACATTGAGGACATTG |
6: 145,173,785 |
|
probably benign |
Homo |
Mamld1 |
GCAACA |
GCAACAACA |
X: 71,118,812 |
|
probably benign |
Het |
Mamld1 |
GCA |
GCAACA |
X: 71,118,818 |
|
probably benign |
Het |
Mast4 |
TGG |
TGGGGGCGG |
13: 102,736,312 |
|
probably benign |
Het |
Mast4 |
GGACAAGCTGTGAGTTGGGGAACCCGGGAG |
GG |
13: 102,739,247 |
|
probably null |
Homo |
Med12l |
GCA |
GCACCA |
3: 59,275,977 |
|
probably benign |
Het |
Mn1 |
CAG |
CAGAAG |
5: 111,419,702 |
|
probably benign |
Het |
Morf4l2 |
T |
C |
X: 136,733,622 |
K286E |
probably benign |
Het |
Msantd4 |
A |
T |
9: 4,384,937 |
I221F |
possibly damaging |
Homo |
Mup21 |
TT |
TTTTTATATACT |
4: 62,149,350 |
|
probably benign |
Het |
Nacad |
A |
ACCAGGG |
11: 6,599,749 |
|
probably benign |
Het |
Nacad |
TCAGGG |
TCAGGGACAGGG |
11: 6,599,756 |
|
probably benign |
Het |
Nacad |
C |
CAGGGTA |
11: 6,599,763 |
|
probably benign |
Het |
Nars |
CCACTCAC |
CCAC |
18: 64,510,445 |
|
probably benign |
Homo |
Ndufc2 |
C |
T |
7: 97,400,274 |
P29L |
probably damaging |
Het |
Nkx2-6 |
C |
T |
14: 69,175,229 |
T282M |
probably damaging |
Homo |
Noc2l |
AGGC |
AGGCGGC |
4: 156,240,092 |
|
probably benign |
Homo |
Noc2l |
CTG |
CTGGTG |
4: 156,240,098 |
|
probably benign |
Het |
Nolc1 |
CAG |
CAGAAGCAGAAG |
19: 46,081,356 |
|
probably benign |
Het |
Nolc1 |
AGC |
AGCAGCAGCGGC |
19: 46,081,375 |
|
probably benign |
Het |
Olfr313 |
T |
A |
11: 58,817,440 |
V144D |
possibly damaging |
Homo |
Olfr418 |
GGGCTGCTTGTGGCAAT |
G |
1: 173,270,630 |
|
probably null |
Het |
Olfr547 |
A |
AAACCG |
7: 102,535,681 |
|
probably null |
Homo |
Olfr585 |
T |
TTAC |
7: 103,098,309 |
|
probably benign |
Homo |
Olfr624 |
AG |
AGAGG |
7: 103,670,966 |
|
probably benign |
Homo |
Patl2 |
CTG |
CTGGTG |
2: 122,126,139 |
|
probably benign |
Het |
Patl2 |
GCT |
GCTTCT |
2: 122,126,141 |
|
probably benign |
Het |
Patl2 |
GC |
GCTTC |
2: 122,126,144 |
|
probably benign |
Het |
Patl2 |
C |
CTGA |
2: 122,126,145 |
|
probably benign |
Het |
Pdik1l |
ACCACC |
ACCACCCCCACC |
4: 134,279,506 |
|
probably benign |
Homo |
Phc1 |
TG |
TGCTGCGG |
6: 122,323,600 |
|
probably benign |
Het |
Phf3 |
ACTGCCGCTCCCGCTCC |
AC |
1: 30,805,023 |
|
probably benign |
Het |
Pick1 |
TTC |
TTCTC |
15: 79,255,946 |
|
probably null |
Homo |
Piezo1 |
G |
A |
8: 122,495,569 |
R503W |
probably damaging |
Homo |
Pik3ap1 |
AG |
AGGGG |
19: 41,281,945 |
|
probably benign |
Homo |
Pik3c2g |
AGAGG |
AGAGGGAGG |
6: 139,635,654 |
|
probably null |
Homo |
Pitrm1 |
TTTTA |
T |
13: 6,560,596 |
|
probably benign |
Homo |
Pogz |
GTAAT |
G |
3: 94,874,695 |
|
probably benign |
Het |
Ppp1r3f |
C |
A |
X: 7,560,336 |
G562V |
probably damaging |
Homo |
Ppp2r5c |
G |
T |
12: 110,540,738 |
|
probably null |
Homo |
Prag1 |
CCGC |
CCGCCGC |
8: 36,103,883 |
|
probably benign |
Homo |
Prr13 |
CACT |
CACTACT |
15: 102,462,171 |
|
probably benign |
Homo |
Prr13 |
CTC |
CTCTTC |
15: 102,462,176 |
|
probably benign |
Homo |
Ptms |
TCT |
TCTCCT |
6: 124,914,454 |
|
probably benign |
Homo |
Ptpn23 |
G |
T |
9: 110,387,633 |
P1052T |
probably benign |
Homo |
Raph1 |
GG |
GGGGG |
1: 60,489,267 |
|
probably benign |
Homo |
Rpa1 |
TGCTGCC |
T |
11: 75,318,519 |
|
probably benign |
Het |
Rpgrip1 |
GGA |
GGATGA |
14: 52,149,394 |
|
probably benign |
Het |
Rpgrip1 |
GGAAGAAGA |
GGA |
14: 52,149,544 |
|
probably benign |
Het |
Rps19 |
AGCGG |
AG |
7: 24,888,996 |
|
probably benign |
Homo |
Rsf1 |
G |
GACC |
7: 97,579,909 |
|
probably benign |
Homo |
Serpina3m |
A |
G |
12: 104,358,623 |
|
probably null |
Homo |
Setd1a |
TGGTGGTGGT |
TGGTGGTGGTGGTGGTGGT |
7: 127,785,307 |
|
probably benign |
Homo |
Setd1a |
TAGTGGTGG |
TAGTGGTGGGAGTGGTGG |
7: 127,785,316 |
|
probably benign |
Het |
Sfswap |
ACTCAGCCC |
ACTCAGCCCCCTCAGCCC |
5: 129,569,751 |
|
probably benign |
Het |
Sh3pxd2b |
CCTGTG |
CCTGTGTCTGTG |
11: 32,423,055 |
|
probably benign |
Het |
Sh3pxd2b |
GCCTGT |
GCCTGTGCCTGT |
11: 32,423,060 |
|
probably benign |
Homo |
Shroom4 |
GCAGCAACA |
GCA |
X: 6,624,074 |
|
probably benign |
Het |
Six3 |
GCG |
GCGTCG |
17: 85,621,358 |
|
probably benign |
Het |
Six3 |
CG |
CGGGG |
17: 85,621,371 |
|
probably benign |
Het |
Skint8 |
C |
T |
4: 111,938,902 |
L258F |
probably benign |
Homo |
Smoc2 |
AGTT |
A |
17: 14,401,562 |
|
probably benign |
Homo |
Smpx |
CCCCCA |
C |
X: 157,720,924 |
|
probably benign |
Homo |
Snx1 |
TC |
TCTGC |
9: 66,104,929 |
|
probably benign |
Homo |
Snx1 |
C |
CTTT |
9: 66,104,930 |
|
probably benign |
Homo |
Sp110 |
CT |
CTAAT |
1: 85,587,489 |
|
probably benign |
Het |
Spaca1 |
GCTCTC |
GCTCTCCCTCTC |
4: 34,049,844 |
|
probably benign |
Het |
Spaca1 |
CGCTCT |
CGCTCTTGCTCT |
4: 34,049,849 |
|
probably benign |
Het |
Spag17 |
AGG |
AGGTGG |
3: 100,056,254 |
|
probably benign |
Het |
Spag17 |
GGA |
GGACGA |
3: 100,056,255 |
|
probably benign |
Het |
Srebf2 |
G |
T |
15: 82,185,335 |
A693S |
probably damaging |
Homo |
Sry |
T |
TGGG |
Y: 2,662,841 |
|
probably benign |
Homo |
Stard8 |
AGG |
AGGTGG |
X: 99,066,513 |
|
probably benign |
Het |
Stard8 |
AGG |
AGGTGG |
X: 99,066,525 |
|
probably benign |
Het |
Stk10 |
CCCA |
C |
11: 32,614,520 |
|
probably benign |
Homo |
Tap2 |
ACTG |
ACTGCTG |
17: 34,205,699 |
|
probably benign |
Homo |
Tbc1d5 |
G |
C |
17: 50,799,931 |
H532Q |
probably benign |
Homo |
Tbc1d5 |
C |
G |
17: 50,799,943 |
Q528H |
probably benign |
Homo |
Tfeb |
GCA |
GCAACA |
17: 47,786,094 |
|
probably benign |
Het |
Tmcc1 |
G |
A |
6: 116,193,380 |
|
probably benign |
Homo |
Tob1 |
AGC |
AGCCGC |
11: 94,214,472 |
|
probably benign |
Het |
Tpsab1 |
TTGCACCTCCT |
TT |
17: 25,343,782 |
|
probably benign |
Het |
Trav15-2-dv6-2 |
GAA |
GAATAA |
14: 53,649,754 |
|
probably null |
Het |
Trav15-2-dv6-2 |
G |
GAAC |
14: 53,649,757 |
|
probably benign |
Homo |
Trim16 |
GTGA |
GTGATGA |
11: 62,820,689 |
|
probably benign |
Homo |
Tsen2 |
AGG |
AGGCGG |
6: 115,560,066 |
|
probably benign |
Homo |
Ubtf |
TC |
TCCGC |
11: 102,306,959 |
|
probably benign |
Het |
Vmn1r124 |
G |
T |
7: 21,259,936 |
Q228K |
possibly damaging |
Het |
Vmn1r71 |
A |
C |
7: 10,748,121 |
S147R |
probably benign |
Homo |
Vmn2r99 |
G |
A |
17: 19,394,285 |
G756R |
probably damaging |
Homo |
Vps13b |
G |
T |
15: 35,846,957 |
A2629S |
probably damaging |
Homo |
Wdr75 |
AAATAA |
AAA |
1: 45,823,404 |
|
probably benign |
Homo |
Zfp111 |
T |
G |
7: 24,199,037 |
K383T |
probably damaging |
Homo |
Zfp111 |
A |
ATCG |
7: 24,199,807 |
|
probably benign |
Homo |
Zfp26 |
C |
A |
9: 20,438,546 |
A241S |
probably benign |
Homo |
Zfp282 |
CGG |
CGGTGG |
6: 47,904,790 |
|
probably benign |
Het |
Zfp335 |
CTC |
CTCTTC |
2: 164,907,474 |
|
probably benign |
Het |
Zfp335 |
TCC |
TCCACC |
2: 164,907,478 |
|
probably benign |
Het |
Zfp459 |
TGA |
TGAGAGA |
13: 67,408,274 |
|
probably null |
Homo |
Zfp459 |
GA |
GAGTTA |
13: 67,408,275 |
|
probably null |
Homo |
Zfp459 |
A |
AGTGG |
13: 67,408,276 |
|
probably null |
Homo |
Zfp462 |
ACC |
ACCTCAGCCACAGCCGCC |
4: 55,009,760 |
|
probably benign |
Het |
Zfp462 |
CC |
CCTCAGCCACAGCCATC |
4: 55,009,761 |
|
probably benign |
Het |
Zfp598 |
CCACAGGC |
CC |
17: 24,679,372 |
|
probably benign |
Het |
Zfp598 |
ACCACC |
ACCACCCCCACC |
17: 24,680,782 |
|
probably benign |
Het |
Zfp683 |
AG |
AGGGG |
4: 134,058,879 |
|
probably benign |
Homo |
|