Incidental Mutation 'R7131:Dnah7c'
| ID |
552615 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Dnah7c
|
| Ensembl Gene |
ENSMUSG00000101337 |
| Gene Name |
dynein, axonemal, heavy chain 7C |
| Synonyms |
Dnahc7c |
| MMRRC Submission |
045216-MU
|
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.371)
|
| Stock # |
R7131 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
46464752-46846636 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 46720932 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Alanine to Serine
at position 2819
(A2819S)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000140430
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000189749]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000189749
AA Change: A2819S
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
| SMART Domains |
Protein: ENSMUSP00000140430
Gene: ENSMUSG00000101337
AA Change: A2819S
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
2 |
15 |
N/A |
INTRINSIC |
|
low complexity region
|
37 |
48 |
N/A |
INTRINSIC |
|
coiled coil region
|
714 |
746 |
N/A |
INTRINSIC |
|
Pfam:DHC_N2
|
754 |
1167 |
2.2e-138 |
PFAM |
|
AAA
|
1320 |
1459 |
4e-3 |
SMART |
|
Blast:AAA
|
1601 |
1829 |
4e-87 |
BLAST |
|
AAA
|
1968 |
2116 |
8.7e-4 |
SMART |
|
Pfam:AAA_8
|
2303 |
2574 |
6.2e-73 |
PFAM |
|
Pfam:MT
|
2586 |
2935 |
5.4e-52 |
PFAM |
|
Pfam:AAA_9
|
2953 |
3183 |
7.4e-63 |
PFAM |
|
Pfam:Dynein_heavy
|
3312 |
4021 |
1.3e-250 |
PFAM |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.7%
- 20x: 99.0%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 100 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Aadacl4fm4 |
A |
G |
4: 144,396,637 (GRCm39) |
V365A |
probably damaging |
Het |
| Abca13 |
A |
G |
11: 9,241,893 (GRCm39) |
N1252S |
probably benign |
Het |
| Abcc3 |
A |
T |
11: 94,255,857 (GRCm39) |
F543I |
probably damaging |
Het |
| Adam15 |
T |
A |
3: 89,254,287 (GRCm39) |
Q170L |
possibly damaging |
Het |
| Aldoc |
A |
G |
11: 78,215,282 (GRCm39) |
I19V |
possibly damaging |
Het |
| Aoc1l1 |
T |
A |
6: 48,953,306 (GRCm39) |
Y410* |
probably null |
Het |
| Atrip |
T |
C |
9: 108,889,488 (GRCm39) |
I711M |
probably benign |
Het |
| Brwd1 |
A |
C |
16: 95,867,698 (GRCm39) |
L149R |
probably damaging |
Het |
| Capn9 |
A |
T |
8: 125,303,017 (GRCm39) |
D45V |
probably damaging |
Het |
| Card9 |
G |
A |
2: 26,248,847 (GRCm39) |
R101C |
probably damaging |
Het |
| Ccdc87 |
A |
G |
19: 4,891,785 (GRCm39) |
E759G |
probably damaging |
Het |
| Ccn1 |
T |
C |
3: 145,354,536 (GRCm39) |
D125G |
probably damaging |
Het |
| Cep250 |
T |
C |
2: 155,806,997 (GRCm39) |
M193T |
probably damaging |
Het |
| Cfap54 |
T |
C |
10: 92,656,966 (GRCm39) |
K3029E |
probably benign |
Het |
| Chrna9 |
G |
A |
5: 66,134,484 (GRCm39) |
G445D |
possibly damaging |
Het |
| Cluap1 |
C |
T |
16: 3,758,639 (GRCm39) |
S367L |
probably benign |
Het |
| Col5a1 |
A |
G |
2: 27,819,498 (GRCm39) |
D200G |
unknown |
Het |
| Crhr2 |
T |
C |
6: 55,069,112 (GRCm39) |
N388D |
|
Het |
| Cyp2b23 |
A |
G |
7: 26,380,838 (GRCm39) |
L129P |
probably benign |
Het |
| Dctd |
A |
G |
8: 48,565,075 (GRCm39) |
S67G |
probably benign |
Het |
| Dhtkd1 |
C |
G |
2: 5,908,881 (GRCm39) |
V738L |
probably benign |
Het |
| Dnah17 |
C |
T |
11: 117,970,484 (GRCm39) |
D2173N |
probably benign |
Het |
| Dnai7 |
A |
T |
6: 145,123,132 (GRCm39) |
L578Q |
probably null |
Het |
| Dot1l |
A |
G |
10: 80,628,175 (GRCm39) |
H1071R |
unknown |
Het |
| Dync2h1 |
T |
A |
9: 7,075,786 (GRCm39) |
D3027V |
probably damaging |
Het |
| Efl1 |
A |
G |
7: 82,307,272 (GRCm39) |
Y56C |
probably damaging |
Het |
| Eif4e1b |
A |
T |
13: 54,931,913 (GRCm39) |
R29W |
probably null |
Het |
| Evc2 |
A |
G |
5: 37,567,602 (GRCm39) |
R860G |
probably damaging |
Het |
| Fbxl12 |
G |
A |
9: 20,555,679 (GRCm39) |
|
probably benign |
Het |
| Fibp |
T |
A |
19: 5,511,519 (GRCm39) |
I129N |
probably damaging |
Het |
| Folh1 |
G |
T |
7: 86,375,320 (GRCm39) |
H555Q |
probably damaging |
Het |
| Gcnt4 |
A |
T |
13: 97,083,027 (GRCm39) |
T108S |
probably damaging |
Het |
| H1f7 |
T |
A |
15: 98,154,250 (GRCm39) |
K300* |
probably null |
Het |
| Hecw2 |
A |
T |
1: 53,904,280 (GRCm39) |
V1156E |
probably damaging |
Het |
| Herc3 |
C |
G |
6: 58,864,409 (GRCm39) |
A681G |
probably damaging |
Het |
| Igkv13-84 |
T |
A |
6: 68,916,764 (GRCm39) |
C20* |
probably null |
Het |
| Iho1 |
A |
T |
9: 108,294,619 (GRCm39) |
D98E |
probably benign |
Het |
| Iqca1l |
A |
G |
5: 24,753,954 (GRCm39) |
V435A |
possibly damaging |
Het |
| Ivd |
C |
A |
2: 118,700,255 (GRCm39) |
T94K |
probably damaging |
Het |
| Kank2 |
C |
T |
9: 21,705,975 (GRCm39) |
A348T |
probably benign |
Het |
| Kcnma1 |
T |
C |
14: 23,417,562 (GRCm39) |
Y889C |
probably damaging |
Het |
| Kif13b |
T |
C |
14: 65,010,517 (GRCm39) |
V1272A |
probably damaging |
Het |
| Kmt2d |
GCTGCTGCT |
GCTGCTGCTCCTGCTGCT |
15: 98,747,497 (GRCm39) |
|
probably benign |
Het |
| Kmt5b |
T |
A |
19: 3,865,412 (GRCm39) |
D825E |
probably benign |
Het |
| Krt39 |
C |
T |
11: 99,411,697 (GRCm39) |
A130T |
probably benign |
Het |
| Krtap4-9 |
C |
T |
11: 99,676,283 (GRCm39) |
T68I |
unknown |
Het |
| Lmbr1l |
A |
T |
15: 98,804,204 (GRCm39) |
V365E |
probably benign |
Het |
| Lonp1 |
C |
T |
17: 56,924,814 (GRCm39) |
R531Q |
probably damaging |
Het |
| Mecom |
T |
A |
3: 30,035,094 (GRCm39) |
H194L |
probably damaging |
Het |
| Mlx |
C |
T |
11: 100,980,068 (GRCm39) |
H188Y |
probably damaging |
Het |
| Mrps10 |
T |
C |
17: 47,685,940 (GRCm39) |
S77P |
probably damaging |
Het |
| Mst1 |
A |
G |
9: 107,962,130 (GRCm39) |
E716G |
probably null |
Het |
| Mttp |
C |
T |
3: 137,821,893 (GRCm39) |
V210I |
probably benign |
Het |
| Mug2 |
T |
C |
6: 122,052,206 (GRCm39) |
V988A |
probably damaging |
Het |
| Ndufb6 |
A |
G |
4: 40,279,336 (GRCm39) |
M1T |
probably null |
Het |
| Neurog1 |
A |
T |
13: 56,399,563 (GRCm39) |
N61K |
probably benign |
Het |
| Nlrp14 |
A |
G |
7: 106,784,021 (GRCm39) |
D581G |
possibly damaging |
Het |
| Nlrp4a |
C |
A |
7: 26,149,258 (GRCm39) |
N288K |
probably benign |
Het |
| Notch3 |
T |
A |
17: 32,363,191 (GRCm39) |
H1264L |
probably benign |
Het |
| Or1e25 |
A |
T |
11: 73,493,562 (GRCm39) |
D52V |
possibly damaging |
Het |
| Or1e34 |
A |
T |
11: 73,778,780 (GRCm39) |
C139* |
probably null |
Het |
| Or3a1c |
A |
G |
11: 74,046,606 (GRCm39) |
M209V |
probably benign |
Het |
| Patl2 |
A |
T |
2: 121,952,263 (GRCm39) |
|
probably null |
Het |
| Pfkfb4 |
A |
G |
9: 108,836,370 (GRCm39) |
T133A |
probably benign |
Het |
| Pla2g4f |
T |
C |
2: 120,135,035 (GRCm39) |
E471G |
probably null |
Het |
| Postn |
T |
C |
3: 54,270,056 (GRCm39) |
V45A |
probably damaging |
Het |
| Ppan |
T |
A |
9: 20,802,450 (GRCm39) |
V257E |
possibly damaging |
Het |
| Ptcra |
C |
G |
17: 47,074,522 (GRCm39) |
A7P |
probably damaging |
Het |
| Ptprd |
C |
T |
4: 75,984,577 (GRCm39) |
R523H |
probably damaging |
Het |
| Pycr3 |
A |
T |
15: 75,790,544 (GRCm39) |
I105N |
possibly damaging |
Het |
| Rfx1 |
C |
A |
8: 84,821,708 (GRCm39) |
Q815K |
probably damaging |
Het |
| Rfx3 |
T |
A |
19: 27,746,028 (GRCm39) |
K668* |
probably null |
Het |
| Ryr2 |
A |
T |
13: 11,655,213 (GRCm39) |
D3661E |
possibly damaging |
Het |
| Ryr2 |
A |
G |
13: 11,683,697 (GRCm39) |
|
probably null |
Het |
| Sec23ip |
T |
A |
7: 128,381,364 (GRCm39) |
S974T |
probably damaging |
Het |
| Semp2l2a |
A |
T |
8: 13,886,982 (GRCm39) |
W370R |
probably damaging |
Het |
| Setbp1 |
A |
G |
18: 79,130,175 (GRCm39) |
F19S |
probably benign |
Het |
| Setd1a |
AAGCAGCAGCAGCAGCAGCAG |
AAGCAGCAGCAGCAGCAG |
7: 127,395,590 (GRCm39) |
|
probably benign |
Het |
| Sh3pxd2b |
A |
G |
11: 32,372,072 (GRCm39) |
K413R |
probably damaging |
Het |
| Slc39a12 |
T |
C |
2: 14,454,614 (GRCm39) |
V544A |
probably damaging |
Het |
| Slc6a7 |
T |
C |
18: 61,135,274 (GRCm39) |
Y418C |
probably damaging |
Het |
| Snx19 |
T |
G |
9: 30,339,189 (GRCm39) |
I109S |
probably damaging |
Het |
| Spart |
T |
C |
3: 55,029,220 (GRCm39) |
|
probably null |
Het |
| Sptbn2 |
A |
T |
19: 4,799,488 (GRCm39) |
Q2097L |
probably null |
Het |
| Syne1 |
T |
C |
10: 5,178,221 (GRCm39) |
K4751R |
probably damaging |
Het |
| Tigit |
C |
A |
16: 43,482,615 (GRCm39) |
G40C |
probably damaging |
Het |
| Tmem181a |
T |
A |
17: 6,348,247 (GRCm39) |
I264K |
probably damaging |
Het |
| Tom1 |
T |
A |
8: 75,783,877 (GRCm39) |
I287N |
possibly damaging |
Het |
| Top2a |
G |
A |
11: 98,895,008 (GRCm39) |
P864L |
possibly damaging |
Het |
| Trmt44 |
A |
T |
5: 35,728,410 (GRCm39) |
V290E |
probably damaging |
Het |
| Try4 |
T |
C |
6: 41,281,337 (GRCm39) |
I93T |
probably benign |
Het |
| Usp24 |
T |
A |
4: 106,239,500 (GRCm39) |
H1147Q |
possibly damaging |
Het |
| Uspl1 |
A |
T |
5: 149,130,745 (GRCm39) |
R109S |
probably benign |
Het |
| Vav3 |
T |
A |
3: 109,571,662 (GRCm39) |
F755I |
probably damaging |
Het |
| Vezt |
A |
T |
10: 93,806,409 (GRCm39) |
Y667* |
probably null |
Het |
| Vmn1r231 |
T |
A |
17: 21,110,140 (GRCm39) |
L258F |
possibly damaging |
Het |
| Zfp207 |
T |
C |
11: 80,286,354 (GRCm39) |
M489T |
unknown |
Het |
| Zfp462 |
A |
G |
4: 55,009,380 (GRCm39) |
T449A |
probably benign |
Het |
| Zfp956 |
C |
A |
6: 47,932,781 (GRCm39) |
Q19K |
probably benign |
Het |
| Zkscan8 |
A |
T |
13: 21,709,443 (GRCm39) |
W152R |
probably damaging |
Het |
|
| Other mutations in Dnah7c |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00559:Dnah7c
|
APN |
1 |
46,846,449 (GRCm39) |
missense |
possibly damaging |
0.72 |
|
IGL02958:Dnah7c
|
APN |
1 |
46,696,271 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL03035:Dnah7c
|
APN |
1 |
46,563,277 (GRCm39) |
missense |
probably benign |
0.37 |
|
IGL03161:Dnah7c
|
APN |
1 |
46,506,456 (GRCm39) |
missense |
probably benign |
0.20 |
|
IGL03178:Dnah7c
|
APN |
1 |
46,506,525 (GRCm39) |
missense |
probably benign |
|
|
IGL03052:Dnah7c
|
UTSW |
1 |
46,671,309 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0751:Dnah7c
|
UTSW |
1 |
46,505,065 (GRCm39) |
missense |
probably benign |
|
|
R1029:Dnah7c
|
UTSW |
1 |
46,651,881 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3104:Dnah7c
|
UTSW |
1 |
46,837,439 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R3977:Dnah7c
|
UTSW |
1 |
46,668,071 (GRCm39) |
missense |
possibly damaging |
0.75 |
|
R4003:Dnah7c
|
UTSW |
1 |
46,720,977 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4133:Dnah7c
|
UTSW |
1 |
46,705,150 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4303:Dnah7c
|
UTSW |
1 |
46,787,738 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4329:Dnah7c
|
UTSW |
1 |
46,688,441 (GRCm39) |
missense |
probably benign |
0.33 |
|
R4434:Dnah7c
|
UTSW |
1 |
46,705,442 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4457:Dnah7c
|
UTSW |
1 |
46,779,781 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4470:Dnah7c
|
UTSW |
1 |
46,787,795 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R4507:Dnah7c
|
UTSW |
1 |
46,805,771 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4527:Dnah7c
|
UTSW |
1 |
46,572,091 (GRCm39) |
missense |
probably benign |
0.34 |
|
R4571:Dnah7c
|
UTSW |
1 |
46,572,376 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4589:Dnah7c
|
UTSW |
1 |
46,553,743 (GRCm39) |
nonsense |
probably null |
|
|
R4731:Dnah7c
|
UTSW |
1 |
46,809,333 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4732:Dnah7c
|
UTSW |
1 |
46,809,333 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4733:Dnah7c
|
UTSW |
1 |
46,809,333 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4747:Dnah7c
|
UTSW |
1 |
46,572,328 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4845:Dnah7c
|
UTSW |
1 |
46,832,692 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4873:Dnah7c
|
UTSW |
1 |
46,728,085 (GRCm39) |
missense |
probably benign |
|
|
R4875:Dnah7c
|
UTSW |
1 |
46,728,085 (GRCm39) |
missense |
probably benign |
|
|
R4916:Dnah7c
|
UTSW |
1 |
46,634,168 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5241:Dnah7c
|
UTSW |
1 |
46,569,660 (GRCm39) |
missense |
probably benign |
|
|
R5279:Dnah7c
|
UTSW |
1 |
46,558,429 (GRCm39) |
missense |
probably benign |
0.14 |
|
R5327:Dnah7c
|
UTSW |
1 |
46,704,728 (GRCm39) |
missense |
probably benign |
0.05 |
|
R5546:Dnah7c
|
UTSW |
1 |
46,705,477 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5605:Dnah7c
|
UTSW |
1 |
46,837,395 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R5637:Dnah7c
|
UTSW |
1 |
46,799,521 (GRCm39) |
splice site |
probably null |
|
|
R5639:Dnah7c
|
UTSW |
1 |
46,778,828 (GRCm39) |
missense |
probably benign |
|
|
R5663:Dnah7c
|
UTSW |
1 |
46,574,308 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5718:Dnah7c
|
UTSW |
1 |
46,787,826 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R5759:Dnah7c
|
UTSW |
1 |
46,654,527 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5771:Dnah7c
|
UTSW |
1 |
46,678,825 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5784:Dnah7c
|
UTSW |
1 |
46,563,228 (GRCm39) |
missense |
possibly damaging |
0.80 |
|
R5800:Dnah7c
|
UTSW |
1 |
46,686,175 (GRCm39) |
missense |
probably benign |
0.01 |
|
R5933:Dnah7c
|
UTSW |
1 |
46,558,375 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5948:Dnah7c
|
UTSW |
1 |
46,711,657 (GRCm39) |
missense |
probably benign |
0.21 |
|
R6034:Dnah7c
|
UTSW |
1 |
46,496,418 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6034:Dnah7c
|
UTSW |
1 |
46,496,418 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6487:Dnah7c
|
UTSW |
1 |
46,808,284 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6536:Dnah7c
|
UTSW |
1 |
46,697,450 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6614:Dnah7c
|
UTSW |
1 |
46,688,511 (GRCm39) |
missense |
probably benign |
|
|
R6614:Dnah7c
|
UTSW |
1 |
46,688,500 (GRCm39) |
missense |
probably benign |
|
|
R6615:Dnah7c
|
UTSW |
1 |
46,688,511 (GRCm39) |
missense |
probably benign |
|
|
R6615:Dnah7c
|
UTSW |
1 |
46,554,599 (GRCm39) |
missense |
probably benign |
0.01 |
|
R6615:Dnah7c
|
UTSW |
1 |
46,688,500 (GRCm39) |
missense |
probably benign |
|
|
R6649:Dnah7c
|
UTSW |
1 |
46,688,511 (GRCm39) |
missense |
probably benign |
|
|
R6649:Dnah7c
|
UTSW |
1 |
46,688,500 (GRCm39) |
missense |
probably benign |
|
|
R6650:Dnah7c
|
UTSW |
1 |
46,688,511 (GRCm39) |
missense |
probably benign |
|
|
R6650:Dnah7c
|
UTSW |
1 |
46,688,500 (GRCm39) |
missense |
probably benign |
|
|
R6651:Dnah7c
|
UTSW |
1 |
46,688,511 (GRCm39) |
missense |
probably benign |
|
|
R6651:Dnah7c
|
UTSW |
1 |
46,688,500 (GRCm39) |
missense |
probably benign |
|
|
R6653:Dnah7c
|
UTSW |
1 |
46,688,511 (GRCm39) |
missense |
probably benign |
|
|
R6653:Dnah7c
|
UTSW |
1 |
46,688,500 (GRCm39) |
missense |
probably benign |
|
|
R6714:Dnah7c
|
UTSW |
1 |
46,779,966 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6729:Dnah7c
|
UTSW |
1 |
46,711,681 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R6760:Dnah7c
|
UTSW |
1 |
46,688,500 (GRCm39) |
missense |
probably benign |
|
|
R6760:Dnah7c
|
UTSW |
1 |
46,688,511 (GRCm39) |
missense |
probably benign |
|
|
R6763:Dnah7c
|
UTSW |
1 |
46,668,050 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
R6866:Dnah7c
|
UTSW |
1 |
46,696,403 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6880:Dnah7c
|
UTSW |
1 |
46,566,831 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R6988:Dnah7c
|
UTSW |
1 |
46,705,373 (GRCm39) |
missense |
possibly damaging |
0.68 |
|
R6995:Dnah7c
|
UTSW |
1 |
46,494,973 (GRCm39) |
missense |
probably benign |
0.07 |
|
R7007:Dnah7c
|
UTSW |
1 |
46,571,910 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7086:Dnah7c
|
UTSW |
1 |
46,789,285 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7128:Dnah7c
|
UTSW |
1 |
46,566,645 (GRCm39) |
missense |
probably benign |
|
|
R7135:Dnah7c
|
UTSW |
1 |
46,572,368 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7171:Dnah7c
|
UTSW |
1 |
46,719,898 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7176:Dnah7c
|
UTSW |
1 |
46,469,969 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7221:Dnah7c
|
UTSW |
1 |
46,494,937 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7310:Dnah7c
|
UTSW |
1 |
46,636,127 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7319:Dnah7c
|
UTSW |
1 |
46,819,935 (GRCm39) |
missense |
probably benign |
0.31 |
|
R7319:Dnah7c
|
UTSW |
1 |
46,823,608 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R7404:Dnah7c
|
UTSW |
1 |
46,705,223 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R7452:Dnah7c
|
UTSW |
1 |
46,686,196 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R7515:Dnah7c
|
UTSW |
1 |
46,496,450 (GRCm39) |
missense |
probably benign |
|
|
R7534:Dnah7c
|
UTSW |
1 |
46,809,227 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R7542:Dnah7c
|
UTSW |
1 |
46,823,658 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7605:Dnah7c
|
UTSW |
1 |
46,671,470 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7643:Dnah7c
|
UTSW |
1 |
46,641,973 (GRCm39) |
missense |
probably benign |
|
|
R7770:Dnah7c
|
UTSW |
1 |
46,665,460 (GRCm39) |
splice site |
probably null |
|
|
R7884:Dnah7c
|
UTSW |
1 |
46,830,929 (GRCm39) |
missense |
probably benign |
0.23 |
|
R7899:Dnah7c
|
UTSW |
1 |
46,553,861 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8025:Dnah7c
|
UTSW |
1 |
46,496,456 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8057:Dnah7c
|
UTSW |
1 |
46,728,112 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R8191:Dnah7c
|
UTSW |
1 |
46,646,618 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
R8255:Dnah7c
|
UTSW |
1 |
46,698,589 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8428:Dnah7c
|
UTSW |
1 |
46,711,536 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8441:Dnah7c
|
UTSW |
1 |
46,572,398 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8485:Dnah7c
|
UTSW |
1 |
46,719,952 (GRCm39) |
missense |
probably benign |
0.05 |
|
R8559:Dnah7c
|
UTSW |
1 |
46,764,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8752:Dnah7c
|
UTSW |
1 |
46,711,701 (GRCm39) |
missense |
probably benign |
0.00 |
|
R8869:Dnah7c
|
UTSW |
1 |
46,671,504 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9058:Dnah7c
|
UTSW |
1 |
46,805,816 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9121:Dnah7c
|
UTSW |
1 |
46,816,896 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9121:Dnah7c
|
UTSW |
1 |
46,704,650 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9246:Dnah7c
|
UTSW |
1 |
46,571,934 (GRCm39) |
missense |
possibly damaging |
0.51 |
|
R9319:Dnah7c
|
UTSW |
1 |
46,521,168 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R9388:Dnah7c
|
UTSW |
1 |
46,779,886 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Dnah7c
|
UTSW |
1 |
46,654,441 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Dnah7c
|
UTSW |
1 |
46,506,462 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1176:Dnah7c
|
UTSW |
1 |
46,799,476 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
Z1176:Dnah7c
|
UTSW |
1 |
46,686,152 (GRCm39) |
critical splice acceptor site |
probably null |
|
|
Z1176:Dnah7c
|
UTSW |
1 |
46,678,825 (GRCm39) |
missense |
probably benign |
|
|
Z1177:Dnah7c
|
UTSW |
1 |
46,693,263 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
| Predicted Primers |
PCR Primer
(F):5'- CCACAAGTCTTAACCATCAGTTTTC -3'
(R):5'- GGTGATCCCAGTTCACATTTGC -3'
Sequencing Primer
(F):5'- AGTCCTTGCAAAGAGCA -3'
(R):5'- GCAATTGTCAGCACCTACCTGG -3'
|
| Posted On |
2019-05-15 |
Incidental Mutation