Incidental Mutation 'R8924:Bahcc1'
| ID |
679491 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Bahcc1
|
| Ensembl Gene |
ENSMUSG00000039741 |
| Gene Name |
BAH domain and coiled-coil containing 1 |
| Synonyms |
|
| MMRRC Submission |
068769-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.838)
|
| Stock # |
R8924 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
120123773-120183108 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 120167591 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Leucine to Phenylalanine
at position 1331
(L1331F)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000112827
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044985]
[ENSMUST00000118987]
[ENSMUST00000122148]
|
| AlphaFold |
Q3UHR0 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000044985
AA Change: L1331F
PolyPhen 2
Score 0.071 (Sensitivity: 0.94; Specificity: 0.84)
|
| SMART Domains |
Protein: ENSMUSP00000043643
Gene: ENSMUSG00000039741
AA Change: L1331F
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
46 |
N/A |
INTRINSIC |
|
low complexity region
|
219 |
233 |
N/A |
INTRINSIC |
|
low complexity region
|
351 |
366 |
N/A |
INTRINSIC |
|
low complexity region
|
756 |
778 |
N/A |
INTRINSIC |
|
low complexity region
|
811 |
821 |
N/A |
INTRINSIC |
|
low complexity region
|
882 |
890 |
N/A |
INTRINSIC |
|
coiled coil region
|
931 |
976 |
N/A |
INTRINSIC |
|
low complexity region
|
1042 |
1059 |
N/A |
INTRINSIC |
|
low complexity region
|
1127 |
1139 |
N/A |
INTRINSIC |
|
low complexity region
|
1172 |
1183 |
N/A |
INTRINSIC |
|
low complexity region
|
1267 |
1277 |
N/A |
INTRINSIC |
|
coiled coil region
|
1346 |
1373 |
N/A |
INTRINSIC |
|
coiled coil region
|
1437 |
1486 |
N/A |
INTRINSIC |
|
low complexity region
|
1706 |
1711 |
N/A |
INTRINSIC |
|
low complexity region
|
1729 |
1740 |
N/A |
INTRINSIC |
|
low complexity region
|
1746 |
1764 |
N/A |
INTRINSIC |
|
low complexity region
|
1865 |
1891 |
N/A |
INTRINSIC |
|
low complexity region
|
2088 |
2104 |
N/A |
INTRINSIC |
|
low complexity region
|
2135 |
2158 |
N/A |
INTRINSIC |
|
low complexity region
|
2209 |
2224 |
N/A |
INTRINSIC |
|
low complexity region
|
2225 |
2245 |
N/A |
INTRINSIC |
|
low complexity region
|
2317 |
2332 |
N/A |
INTRINSIC |
|
low complexity region
|
2348 |
2387 |
N/A |
INTRINSIC |
|
low complexity region
|
2401 |
2410 |
N/A |
INTRINSIC |
|
low complexity region
|
2429 |
2447 |
N/A |
INTRINSIC |
|
BAH
|
2517 |
2637 |
4.19e-20 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000118987
AA Change: L1331F
PolyPhen 2
Score 0.089 (Sensitivity: 0.93; Specificity: 0.85)
|
| SMART Domains |
Protein: ENSMUSP00000112784
Gene: ENSMUSG00000039741
AA Change: L1331F
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
46 |
N/A |
INTRINSIC |
|
low complexity region
|
219 |
233 |
N/A |
INTRINSIC |
|
low complexity region
|
351 |
366 |
N/A |
INTRINSIC |
|
low complexity region
|
756 |
778 |
N/A |
INTRINSIC |
|
low complexity region
|
811 |
821 |
N/A |
INTRINSIC |
|
low complexity region
|
882 |
890 |
N/A |
INTRINSIC |
|
coiled coil region
|
931 |
976 |
N/A |
INTRINSIC |
|
low complexity region
|
1042 |
1059 |
N/A |
INTRINSIC |
|
low complexity region
|
1127 |
1139 |
N/A |
INTRINSIC |
|
low complexity region
|
1172 |
1183 |
N/A |
INTRINSIC |
|
low complexity region
|
1267 |
1277 |
N/A |
INTRINSIC |
|
coiled coil region
|
1346 |
1373 |
N/A |
INTRINSIC |
|
coiled coil region
|
1437 |
1486 |
N/A |
INTRINSIC |
|
low complexity region
|
1706 |
1711 |
N/A |
INTRINSIC |
|
low complexity region
|
1729 |
1740 |
N/A |
INTRINSIC |
|
low complexity region
|
1746 |
1764 |
N/A |
INTRINSIC |
|
low complexity region
|
1865 |
1891 |
N/A |
INTRINSIC |
|
low complexity region
|
2088 |
2104 |
N/A |
INTRINSIC |
|
low complexity region
|
2135 |
2158 |
N/A |
INTRINSIC |
|
low complexity region
|
2209 |
2224 |
N/A |
INTRINSIC |
|
low complexity region
|
2225 |
2245 |
N/A |
INTRINSIC |
|
low complexity region
|
2317 |
2332 |
N/A |
INTRINSIC |
|
low complexity region
|
2348 |
2387 |
N/A |
INTRINSIC |
|
low complexity region
|
2401 |
2410 |
N/A |
INTRINSIC |
|
low complexity region
|
2429 |
2447 |
N/A |
INTRINSIC |
|
BAH
|
2517 |
2637 |
4.19e-20 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000122148
AA Change: L1331F
PolyPhen 2
Score 0.089 (Sensitivity: 0.93; Specificity: 0.85)
|
| SMART Domains |
Protein: ENSMUSP00000112827
Gene: ENSMUSG00000039741
AA Change: L1331F
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
17 |
46 |
N/A |
INTRINSIC |
|
low complexity region
|
219 |
233 |
N/A |
INTRINSIC |
|
low complexity region
|
351 |
366 |
N/A |
INTRINSIC |
|
low complexity region
|
756 |
778 |
N/A |
INTRINSIC |
|
low complexity region
|
811 |
821 |
N/A |
INTRINSIC |
|
low complexity region
|
882 |
890 |
N/A |
INTRINSIC |
|
coiled coil region
|
931 |
976 |
N/A |
INTRINSIC |
|
low complexity region
|
1042 |
1059 |
N/A |
INTRINSIC |
|
low complexity region
|
1127 |
1139 |
N/A |
INTRINSIC |
|
low complexity region
|
1172 |
1183 |
N/A |
INTRINSIC |
|
low complexity region
|
1267 |
1277 |
N/A |
INTRINSIC |
|
coiled coil region
|
1346 |
1373 |
N/A |
INTRINSIC |
|
coiled coil region
|
1437 |
1486 |
N/A |
INTRINSIC |
|
low complexity region
|
1706 |
1711 |
N/A |
INTRINSIC |
|
low complexity region
|
1729 |
1740 |
N/A |
INTRINSIC |
|
low complexity region
|
1746 |
1764 |
N/A |
INTRINSIC |
|
low complexity region
|
1865 |
1891 |
N/A |
INTRINSIC |
|
low complexity region
|
2088 |
2104 |
N/A |
INTRINSIC |
|
low complexity region
|
2135 |
2158 |
N/A |
INTRINSIC |
|
low complexity region
|
2209 |
2224 |
N/A |
INTRINSIC |
|
low complexity region
|
2225 |
2245 |
N/A |
INTRINSIC |
|
low complexity region
|
2317 |
2332 |
N/A |
INTRINSIC |
|
low complexity region
|
2348 |
2387 |
N/A |
INTRINSIC |
|
low complexity region
|
2401 |
2410 |
N/A |
INTRINSIC |
|
low complexity region
|
2429 |
2447 |
N/A |
INTRINSIC |
|
BAH
|
2517 |
2637 |
4.19e-20 |
SMART |
|
| Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
| Validation Efficiency |
98% (88/90) |
| MGI Phenotype |
PHENOTYPE: Homozygous mutation of this gene results in perinatal lethality for the majority of mutants. Those that survive exhibit hind leg motor dysfunction. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(26) : Targeted, knock-out(2) Gene trapped(24) |
| Other mutations in this stock |
Total: 90 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca8b |
A |
G |
11: 109,838,003 (GRCm39) |
V1145A |
probably benign |
Het |
| Ank1 |
T |
C |
8: 23,589,011 (GRCm39) |
M562T |
probably benign |
Het |
| Atn1 |
A |
T |
6: 124,722,211 (GRCm39) |
S881T |
probably benign |
Het |
| B3galt1 |
C |
T |
2: 67,949,059 (GRCm39) |
T258I |
probably benign |
Het |
| Capn12 |
G |
A |
7: 28,582,628 (GRCm39) |
V168M |
probably damaging |
Het |
| Card14 |
T |
C |
11: 119,216,930 (GRCm39) |
V338A |
possibly damaging |
Het |
| Cd27 |
T |
C |
6: 125,213,432 (GRCm39) |
|
probably benign |
Het |
| Cd37 |
A |
G |
7: 44,888,109 (GRCm39) |
L37P |
probably damaging |
Het |
| Cd96 |
A |
G |
16: 45,919,385 (GRCm39) |
L212P |
probably damaging |
Het |
| Celsr1 |
T |
C |
15: 85,916,671 (GRCm39) |
E434G |
possibly damaging |
Het |
| Cep152 |
A |
G |
2: 125,444,778 (GRCm39) |
M456T |
possibly damaging |
Het |
| Ces3b |
G |
A |
8: 105,811,619 (GRCm39) |
R45H |
probably benign |
Het |
| Cfap54 |
T |
G |
10: 92,837,685 (GRCm39) |
T1072P |
probably damaging |
Het |
| Chodl |
A |
T |
16: 78,738,659 (GRCm39) |
M172L |
possibly damaging |
Het |
| Cilp2 |
A |
G |
8: 70,339,108 (GRCm39) |
S47P |
probably damaging |
Het |
| Clasrp |
T |
C |
7: 19,318,232 (GRCm39) |
I596V |
unknown |
Het |
| Clcn2 |
C |
T |
16: 20,530,930 (GRCm39) |
V267I |
probably damaging |
Het |
| Cntln |
T |
A |
4: 84,806,936 (GRCm39) |
D139E |
probably damaging |
Het |
| Cyp2j12 |
A |
C |
4: 95,994,685 (GRCm39) |
N379K |
probably damaging |
Het |
| Defb21 |
T |
C |
2: 152,416,704 (GRCm39) |
V60A |
possibly damaging |
Het |
| Dnajc16 |
G |
T |
4: 141,494,018 (GRCm39) |
S543* |
probably null |
Het |
| Efcab12 |
G |
T |
6: 115,800,664 (GRCm39) |
H120N |
probably benign |
Het |
| Efcab3 |
AACTCTA |
AA |
11: 104,806,253 (GRCm39) |
|
probably null |
Het |
| Efl1 |
G |
A |
7: 82,412,161 (GRCm39) |
G850D |
probably benign |
Het |
| Efna1 |
T |
C |
3: 89,183,635 (GRCm39) |
M64V |
probably benign |
Het |
| Eif2ak3 |
T |
C |
6: 70,870,003 (GRCm39) |
W897R |
probably damaging |
Het |
| Eif2ak4 |
T |
A |
2: 118,258,513 (GRCm39) |
F621Y |
probably damaging |
Het |
| Erbin |
C |
A |
13: 103,975,966 (GRCm39) |
E643* |
probably null |
Het |
| Esr1 |
G |
A |
10: 4,807,176 (GRCm39) |
W364* |
probably null |
Het |
| Fam171a2 |
T |
C |
11: 102,330,861 (GRCm39) |
E206G |
possibly damaging |
Het |
| Fam90a1a |
T |
C |
8: 22,451,429 (GRCm39) |
F97L |
probably benign |
Het |
| Fap |
A |
T |
2: 62,378,165 (GRCm39) |
F181I |
probably benign |
Het |
| Fem1b |
T |
C |
9: 62,704,916 (GRCm39) |
N115D |
probably damaging |
Het |
| Gal3st2b |
G |
T |
1: 93,868,653 (GRCm39) |
A295S |
probably benign |
Het |
| Galnt10 |
G |
A |
11: 57,674,681 (GRCm39) |
|
probably benign |
Het |
| Gcfc2 |
T |
C |
6: 81,909,879 (GRCm39) |
V224A |
probably damaging |
Het |
| Gh |
T |
C |
11: 106,191,634 (GRCm39) |
E136G |
probably damaging |
Het |
| Gjd3 |
C |
T |
11: 98,873,325 (GRCm39) |
C173Y |
probably damaging |
Het |
| Gm12695 |
T |
A |
4: 96,651,046 (GRCm39) |
M136L |
probably benign |
Het |
| Gnas |
A |
G |
2: 174,141,277 (GRCm39) |
E482G |
unknown |
Het |
| Gpa33 |
T |
C |
1: 165,980,351 (GRCm39) |
L138P |
probably damaging |
Het |
| Hlf |
T |
C |
11: 90,236,714 (GRCm39) |
D181G |
probably damaging |
Het |
| Irgm1 |
A |
G |
11: 48,756,698 (GRCm39) |
L387S |
probably benign |
Het |
| Kctd1 |
T |
C |
18: 15,102,745 (GRCm39) |
E812G |
possibly damaging |
Het |
| Klra2 |
T |
C |
6: 131,205,214 (GRCm39) |
E209G |
probably benign |
Het |
| Klra3 |
C |
T |
6: 130,312,732 (GRCm39) |
V11M |
probably benign |
Het |
| Klrh1 |
G |
T |
6: 129,745,084 (GRCm39) |
H171N |
probably benign |
Het |
| Kmt2c |
T |
C |
5: 25,503,885 (GRCm39) |
S3808G |
probably benign |
Het |
| Krtap24-1 |
A |
C |
16: 88,408,888 (GRCm39) |
S79R |
probably benign |
Het |
| Limch1 |
T |
A |
5: 67,190,475 (GRCm39) |
H759Q |
probably benign |
Het |
| Map3k4 |
A |
G |
17: 12,490,433 (GRCm39) |
Y333H |
probably benign |
Het |
| Mmel1 |
A |
G |
4: 154,974,091 (GRCm39) |
Y377C |
probably damaging |
Het |
| Ms4a14 |
A |
T |
19: 11,281,113 (GRCm39) |
Y482N |
possibly damaging |
Het |
| Myo9b |
A |
G |
8: 71,801,675 (GRCm39) |
S1277G |
probably benign |
Het |
| Nab1 |
T |
C |
1: 52,529,667 (GRCm39) |
T77A |
possibly damaging |
Het |
| Obsl1 |
T |
C |
1: 75,482,841 (GRCm39) |
S10G |
probably benign |
Het |
| Odc1 |
A |
G |
12: 17,598,329 (GRCm39) |
T157A |
possibly damaging |
Het |
| Or2a5 |
T |
G |
6: 42,873,964 (GRCm39) |
L193R |
probably damaging |
Het |
| Or8b52 |
T |
C |
9: 38,576,780 (GRCm39) |
D120G |
probably damaging |
Het |
| Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
| Plpp1 |
T |
A |
13: 112,943,057 (GRCm39) |
|
probably benign |
Het |
| Prdm13 |
G |
A |
4: 21,679,125 (GRCm39) |
A455V |
possibly damaging |
Het |
| Ptpn13 |
A |
T |
5: 103,739,101 (GRCm39) |
Y2289F |
probably damaging |
Het |
| Ptpn18 |
G |
T |
1: 34,498,966 (GRCm39) |
R21L |
probably benign |
Het |
| Ptprd |
A |
G |
4: 75,916,736 (GRCm39) |
|
probably null |
Het |
| Rcn3 |
G |
T |
7: 44,733,095 (GRCm39) |
D258E |
probably damaging |
Het |
| Ro60 |
C |
T |
1: 143,641,170 (GRCm39) |
|
probably null |
Het |
| Rsf1 |
GCG |
GCGACGGCGCCG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
| Sacs |
T |
A |
14: 61,429,895 (GRCm39) |
H651Q |
probably benign |
Het |
| Sacs |
T |
C |
14: 61,448,702 (GRCm39) |
S3583P |
probably damaging |
Het |
| Scel |
A |
G |
14: 103,829,807 (GRCm39) |
N463S |
possibly damaging |
Het |
| Serpinb2 |
A |
T |
1: 107,443,284 (GRCm39) |
I28F |
possibly damaging |
Het |
| Sin3b |
A |
G |
8: 73,473,131 (GRCm39) |
K484E |
probably benign |
Het |
| Snrnp48 |
T |
A |
13: 38,400,397 (GRCm39) |
V168D |
probably damaging |
Het |
| Snx18 |
T |
G |
13: 113,754,931 (GRCm39) |
M1L |
probably benign |
Het |
| Spata31h1 |
T |
C |
10: 82,131,295 (GRCm39) |
N572D |
probably benign |
Het |
| Srcap |
T |
A |
7: 127,158,204 (GRCm39) |
N2693K |
unknown |
Het |
| Stim1 |
A |
G |
7: 102,078,014 (GRCm39) |
D172G |
|
Het |
| Stip1 |
A |
T |
19: 7,002,687 (GRCm39) |
L414H |
probably damaging |
Het |
| Sun1 |
A |
G |
5: 139,209,390 (GRCm39) |
H40R |
probably damaging |
Het |
| Sva |
T |
A |
6: 42,019,182 (GRCm39) |
D117E |
possibly damaging |
Het |
| Syne2 |
A |
G |
12: 75,943,444 (GRCm39) |
D321G |
probably damaging |
Het |
| Trim45 |
A |
G |
3: 100,835,394 (GRCm39) |
D459G |
probably damaging |
Het |
| Ttc6 |
G |
A |
12: 57,697,790 (GRCm39) |
W43* |
probably null |
Het |
| Ugt2b35 |
A |
G |
5: 87,152,780 (GRCm39) |
T317A |
possibly damaging |
Het |
| Usp32 |
C |
T |
11: 84,916,370 (GRCm39) |
R858Q |
probably damaging |
Het |
| Vmn2r53 |
G |
T |
7: 12,334,752 (GRCm39) |
Q303K |
probably benign |
Het |
| Yeats2 |
T |
C |
16: 19,969,312 (GRCm39) |
|
probably null |
Het |
| Zfp804a |
A |
G |
2: 82,088,747 (GRCm39) |
N859D |
probably benign |
Het |
| Zscan10 |
A |
T |
17: 23,824,580 (GRCm39) |
Q12L |
possibly damaging |
Het |
|
| Other mutations in Bahcc1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00341:Bahcc1
|
APN |
11 |
120,163,130 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00536:Bahcc1
|
APN |
11 |
120,175,871 (GRCm39) |
missense |
probably damaging |
0.96 |
|
IGL01339:Bahcc1
|
APN |
11 |
120,180,338 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01695:Bahcc1
|
APN |
11 |
120,167,435 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01744:Bahcc1
|
APN |
11 |
120,162,563 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL01769:Bahcc1
|
APN |
11 |
120,171,030 (GRCm39) |
splice site |
probably benign |
|
|
IGL01982:Bahcc1
|
APN |
11 |
120,178,299 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02341:Bahcc1
|
APN |
11 |
120,163,346 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02535:Bahcc1
|
APN |
11 |
120,178,362 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
IGL02559:Bahcc1
|
APN |
11 |
120,175,998 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL02579:Bahcc1
|
APN |
11 |
120,176,175 (GRCm39) |
splice site |
probably benign |
|
|
IGL02609:Bahcc1
|
APN |
11 |
120,180,224 (GRCm39) |
missense |
possibly damaging |
0.93 |
|
IGL02678:Bahcc1
|
APN |
11 |
120,163,697 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02800:Bahcc1
|
APN |
11 |
120,163,760 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02963:Bahcc1
|
APN |
11 |
120,165,758 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
IGL03128:Bahcc1
|
APN |
11 |
120,159,260 (GRCm39) |
splice site |
probably benign |
|
|
IGL03242:Bahcc1
|
APN |
11 |
120,159,126 (GRCm39) |
splice site |
probably benign |
|
|
IGL03248:Bahcc1
|
APN |
11 |
120,159,235 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Dimensionality
|
UTSW |
11 |
120,163,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
G1citation:Bahcc1
|
UTSW |
11 |
120,178,547 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0019:Bahcc1
|
UTSW |
11 |
120,180,597 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0040:Bahcc1
|
UTSW |
11 |
120,159,196 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0040:Bahcc1
|
UTSW |
11 |
120,159,196 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0148:Bahcc1
|
UTSW |
11 |
120,159,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0164:Bahcc1
|
UTSW |
11 |
120,175,900 (GRCm39) |
splice site |
probably benign |
|
|
R0321:Bahcc1
|
UTSW |
11 |
120,164,251 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0671:Bahcc1
|
UTSW |
11 |
120,178,146 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0737:Bahcc1
|
UTSW |
11 |
120,163,667 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1452:Bahcc1
|
UTSW |
11 |
120,173,065 (GRCm39) |
splice site |
probably benign |
|
|
R1570:Bahcc1
|
UTSW |
11 |
120,163,009 (GRCm39) |
missense |
possibly damaging |
0.74 |
|
R1914:Bahcc1
|
UTSW |
11 |
120,176,225 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2010:Bahcc1
|
UTSW |
11 |
120,163,604 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2075:Bahcc1
|
UTSW |
11 |
120,162,515 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2085:Bahcc1
|
UTSW |
11 |
120,178,908 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3552:Bahcc1
|
UTSW |
11 |
120,167,598 (GRCm39) |
missense |
possibly damaging |
0.90 |
|
R3711:Bahcc1
|
UTSW |
11 |
120,165,923 (GRCm39) |
missense |
probably benign |
0.27 |
|
R3804:Bahcc1
|
UTSW |
11 |
120,174,184 (GRCm39) |
missense |
probably benign |
0.01 |
|
R4349:Bahcc1
|
UTSW |
11 |
120,150,027 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4557:Bahcc1
|
UTSW |
11 |
120,165,914 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4801:Bahcc1
|
UTSW |
11 |
120,173,051 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4802:Bahcc1
|
UTSW |
11 |
120,173,051 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4908:Bahcc1
|
UTSW |
11 |
120,178,580 (GRCm39) |
missense |
probably benign |
0.36 |
|
R4941:Bahcc1
|
UTSW |
11 |
120,177,491 (GRCm39) |
missense |
probably benign |
|
|
R5217:Bahcc1
|
UTSW |
11 |
120,165,285 (GRCm39) |
nonsense |
probably null |
|
|
R5241:Bahcc1
|
UTSW |
11 |
120,162,229 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5432:Bahcc1
|
UTSW |
11 |
120,178,814 (GRCm39) |
missense |
probably benign |
0.02 |
|
R5696:Bahcc1
|
UTSW |
11 |
120,164,813 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5724:Bahcc1
|
UTSW |
11 |
120,176,192 (GRCm39) |
missense |
possibly damaging |
0.78 |
|
R5725:Bahcc1
|
UTSW |
11 |
120,165,714 (GRCm39) |
missense |
probably benign |
|
|
R5788:Bahcc1
|
UTSW |
11 |
120,177,178 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5893:Bahcc1
|
UTSW |
11 |
120,176,256 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R5900:Bahcc1
|
UTSW |
11 |
120,175,319 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6014:Bahcc1
|
UTSW |
11 |
120,180,615 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6058:Bahcc1
|
UTSW |
11 |
120,178,211 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6107:Bahcc1
|
UTSW |
11 |
120,163,714 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6302:Bahcc1
|
UTSW |
11 |
120,167,634 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6525:Bahcc1
|
UTSW |
11 |
120,176,048 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6550:Bahcc1
|
UTSW |
11 |
120,167,477 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6822:Bahcc1
|
UTSW |
11 |
120,178,547 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6836:Bahcc1
|
UTSW |
11 |
120,162,583 (GRCm39) |
nonsense |
probably null |
|
|
R6846:Bahcc1
|
UTSW |
11 |
120,162,422 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R6916:Bahcc1
|
UTSW |
11 |
120,163,835 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6966:Bahcc1
|
UTSW |
11 |
120,173,985 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7097:Bahcc1
|
UTSW |
11 |
120,163,472 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R7289:Bahcc1
|
UTSW |
11 |
120,171,000 (GRCm39) |
missense |
probably benign |
0.08 |
|
R7441:Bahcc1
|
UTSW |
11 |
120,177,132 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7520:Bahcc1
|
UTSW |
11 |
120,167,031 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
R7556:Bahcc1
|
UTSW |
11 |
120,178,589 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7672:Bahcc1
|
UTSW |
11 |
120,174,172 (GRCm39) |
missense |
possibly damaging |
0.63 |
|
R7791:Bahcc1
|
UTSW |
11 |
120,159,203 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7794:Bahcc1
|
UTSW |
11 |
120,163,507 (GRCm39) |
nonsense |
probably null |
|
|
R7802:Bahcc1
|
UTSW |
11 |
120,165,518 (GRCm39) |
missense |
probably benign |
0.03 |
|
R7946:Bahcc1
|
UTSW |
11 |
120,163,325 (GRCm39) |
missense |
probably benign |
|
|
R7985:Bahcc1
|
UTSW |
11 |
120,163,717 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R8128:Bahcc1
|
UTSW |
11 |
120,163,216 (GRCm39) |
nonsense |
probably null |
|
|
R8131:Bahcc1
|
UTSW |
11 |
120,163,664 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8353:Bahcc1
|
UTSW |
11 |
120,165,251 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8439:Bahcc1
|
UTSW |
11 |
120,165,415 (GRCm39) |
missense |
probably benign |
0.01 |
|
R8710:Bahcc1
|
UTSW |
11 |
120,174,953 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8799:Bahcc1
|
UTSW |
11 |
120,177,173 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8810:Bahcc1
|
UTSW |
11 |
120,164,587 (GRCm39) |
missense |
possibly damaging |
0.76 |
|
R8920:Bahcc1
|
UTSW |
11 |
120,175,331 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9014:Bahcc1
|
UTSW |
11 |
120,173,048 (GRCm39) |
missense |
probably benign |
|
|
R9014:Bahcc1
|
UTSW |
11 |
120,163,715 (GRCm39) |
missense |
probably benign |
0.00 |
|
R9195:Bahcc1
|
UTSW |
11 |
120,167,337 (GRCm39) |
missense |
probably benign |
|
|
R9216:Bahcc1
|
UTSW |
11 |
120,177,514 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9328:Bahcc1
|
UTSW |
11 |
120,165,885 (GRCm39) |
missense |
possibly damaging |
0.61 |
|
R9392:Bahcc1
|
UTSW |
11 |
120,163,513 (GRCm39) |
nonsense |
probably null |
|
|
R9562:Bahcc1
|
UTSW |
11 |
120,150,035 (GRCm39) |
missense |
possibly damaging |
0.87 |
|
R9680:Bahcc1
|
UTSW |
11 |
120,163,286 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R9797:Bahcc1
|
UTSW |
11 |
120,159,147 (GRCm39) |
nonsense |
probably null |
|
|
X0026:Bahcc1
|
UTSW |
11 |
120,162,578 (GRCm39) |
missense |
probably benign |
0.20 |
|
Z1176:Bahcc1
|
UTSW |
11 |
120,175,220 (GRCm39) |
missense |
probably benign |
0.00 |
|
Z1176:Bahcc1
|
UTSW |
11 |
120,167,435 (GRCm39) |
missense |
possibly damaging |
0.89 |
|
Z1177:Bahcc1
|
UTSW |
11 |
120,163,747 (GRCm39) |
missense |
possibly damaging |
0.73 |
|
| Predicted Primers |
PCR Primer
(F):5'- ACAGAAGGTCCCTGATGTGG -3'
(R):5'- AGGCTACCACCTATCTGTCTGAC -3'
Sequencing Primer
(F):5'- CTGATGTGGCCCAGCTAC -3'
(R):5'- TATCTGTCTGACCCCGAGG -3'
|
| Posted On |
2021-08-02 |
Incidental Mutation