Incidental Mutation 'R2509:Shprh'
ID |
251780 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Shprh
|
Ensembl Gene |
ENSMUSG00000090112 |
Gene Name |
SNF2 histone linker PHD RING helicase |
Synonyms |
2610103K11Rik, D230017O13Rik |
MMRRC Submission |
040415-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R2509 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
10 |
Chromosomal Location |
11025171-11093339 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 11042468 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Tyrosine
at position 817
(C817Y)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000125457
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044053]
[ENSMUST00000054814]
[ENSMUST00000159541]
[ENSMUST00000159810]
[ENSMUST00000160461]
|
AlphaFold |
Q7TPQ3 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000044053
AA Change: C817Y
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000039422 Gene: ENSMUSG00000090112 AA Change: C817Y
Domain | Start | End | E-Value | Type |
low complexity region
|
42 |
56 |
N/A |
INTRINSIC |
Blast:DEXDc
|
195 |
250 |
3e-12 |
BLAST |
low complexity region
|
253 |
265 |
N/A |
INTRINSIC |
DEXDc
|
295 |
866 |
4.02e-17 |
SMART |
H15
|
431 |
497 |
3.76e-5 |
SMART |
PHD
|
651 |
698 |
2.33e-5 |
SMART |
low complexity region
|
1393 |
1404 |
N/A |
INTRINSIC |
RING
|
1423 |
1469 |
9.68e-3 |
SMART |
Pfam:Helicase_C
|
1500 |
1613 |
1.6e-8 |
PFAM |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000054814
AA Change: C817Y
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000125849 Gene: ENSMUSG00000090112 AA Change: C817Y
Domain | Start | End | E-Value | Type |
low complexity region
|
42 |
56 |
N/A |
INTRINSIC |
Blast:DEXDc
|
195 |
250 |
3e-12 |
BLAST |
low complexity region
|
253 |
265 |
N/A |
INTRINSIC |
DEXDc
|
295 |
866 |
4.02e-17 |
SMART |
H15
|
431 |
497 |
3.76e-5 |
SMART |
PHD
|
651 |
698 |
2.33e-5 |
SMART |
low complexity region
|
1393 |
1404 |
N/A |
INTRINSIC |
RING
|
1423 |
1469 |
9.68e-3 |
SMART |
SCOP:d1fuka_
|
1504 |
1616 |
6e-8 |
SMART |
Blast:HELICc
|
1533 |
1613 |
4e-46 |
BLAST |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000159541
AA Change: C817Y
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000132870 Gene: ENSMUSG00000090112 AA Change: C817Y
Domain | Start | End | E-Value | Type |
low complexity region
|
42 |
56 |
N/A |
INTRINSIC |
Blast:DEXDc
|
195 |
250 |
3e-12 |
BLAST |
low complexity region
|
253 |
265 |
N/A |
INTRINSIC |
DEXDc
|
295 |
866 |
4.02e-17 |
SMART |
H15
|
431 |
497 |
3.76e-5 |
SMART |
PHD
|
651 |
698 |
2.33e-5 |
SMART |
low complexity region
|
1393 |
1404 |
N/A |
INTRINSIC |
RING
|
1423 |
1469 |
9.68e-3 |
SMART |
SCOP:d1fuka_
|
1504 |
1619 |
4e-8 |
SMART |
Blast:HELICc
|
1533 |
1613 |
6e-46 |
BLAST |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000159553
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000159810
AA Change: C817Y
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000125457 Gene: ENSMUSG00000090112 AA Change: C817Y
Domain | Start | End | E-Value | Type |
low complexity region
|
42 |
56 |
N/A |
INTRINSIC |
Blast:DEXDc
|
195 |
250 |
2e-12 |
BLAST |
low complexity region
|
253 |
265 |
N/A |
INTRINSIC |
DEXDc
|
295 |
866 |
4.02e-17 |
SMART |
H15
|
431 |
497 |
3.76e-5 |
SMART |
PHD
|
651 |
698 |
2.33e-5 |
SMART |
Blast:DEXDc
|
948 |
1026 |
2e-9 |
BLAST |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000160461
|
SMART Domains |
Protein: ENSMUSP00000125127 Gene: ENSMUSG00000090112
Domain | Start | End | E-Value | Type |
PHD
|
131 |
178 |
2.33e-5 |
SMART |
|
Meta Mutation Damage Score |
0.2542 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.4%
- 20x: 95.4%
|
Validation Efficiency |
96% (105/109) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] SHPRH is a ubiquitously expressed protein that contains motifs characteristics of several DNA repair proteins, transcription factors, and helicases. SHPRH is a functional homolog of S. cerevisiae RAD5 (Unk et al., 2006 [PubMed 17108083]).[supplied by OMIM, Mar 2008] PHENOTYPE: The gene product is an E3 ligase involved in poly-ubiquitination of Pcna. Neither homozygous truncation nor KO affect B cell somatic hypermutation or class switching. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
T |
C |
3: 124,200,102 (GRCm39) |
I497V |
probably benign |
Het |
4930571K23Rik |
C |
A |
7: 124,968,311 (GRCm39) |
|
noncoding transcript |
Het |
Abca17 |
G |
T |
17: 24,508,587 (GRCm39) |
|
probably benign |
Het |
Ablim1 |
C |
T |
19: 57,140,791 (GRCm39) |
R196Q |
probably damaging |
Het |
Acot11 |
T |
C |
4: 106,612,516 (GRCm39) |
I379V |
possibly damaging |
Het |
Acot4 |
G |
A |
12: 84,088,647 (GRCm39) |
G165D |
probably damaging |
Het |
Agrn |
A |
T |
4: 156,250,881 (GRCm39) |
|
probably null |
Het |
Ahctf1 |
T |
C |
1: 179,598,258 (GRCm39) |
S945G |
possibly damaging |
Het |
Akr1c13 |
C |
T |
13: 4,248,583 (GRCm39) |
R263C |
probably damaging |
Het |
Arfgap1 |
T |
A |
2: 180,615,846 (GRCm39) |
|
probably benign |
Het |
Arhgef3 |
A |
G |
14: 27,101,633 (GRCm39) |
K103R |
probably damaging |
Het |
Cabp1 |
A |
T |
5: 115,310,843 (GRCm39) |
N211K |
probably damaging |
Het |
Cacna1c |
T |
A |
6: 118,711,943 (GRCm39) |
D261V |
probably damaging |
Het |
Car11 |
G |
A |
7: 45,350,783 (GRCm39) |
G93E |
probably damaging |
Het |
Card10 |
A |
G |
15: 78,664,473 (GRCm39) |
I821T |
probably benign |
Het |
Cast |
T |
C |
13: 74,885,735 (GRCm39) |
I277V |
probably benign |
Het |
Cenpj |
T |
C |
14: 56,769,694 (GRCm39) |
K1165R |
probably null |
Het |
Cenpk |
A |
G |
13: 104,370,675 (GRCm39) |
|
probably null |
Het |
Cfap251 |
A |
G |
5: 123,394,169 (GRCm39) |
K353E |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,230,066 (GRCm39) |
Q1674R |
probably benign |
Het |
Cnnm1 |
T |
A |
19: 43,430,325 (GRCm39) |
V481D |
probably damaging |
Het |
Cracdl |
T |
C |
1: 37,664,381 (GRCm39) |
M506V |
probably benign |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
Cyp2c50 |
G |
A |
19: 40,079,013 (GRCm39) |
V119I |
probably benign |
Het |
Dnah7b |
A |
G |
1: 46,234,447 (GRCm39) |
T1460A |
probably damaging |
Het |
Dnah8 |
G |
A |
17: 30,994,019 (GRCm39) |
D3379N |
probably benign |
Het |
Dnajc4 |
C |
T |
19: 6,968,111 (GRCm39) |
R55H |
probably damaging |
Het |
Ebf4 |
C |
T |
2: 130,148,482 (GRCm39) |
R98* |
probably null |
Het |
Epha4 |
G |
A |
1: 77,488,339 (GRCm39) |
A47V |
possibly damaging |
Het |
Ercc8 |
T |
C |
13: 108,320,251 (GRCm39) |
|
probably benign |
Het |
Exo1 |
T |
C |
1: 175,733,399 (GRCm39) |
F75S |
probably damaging |
Het |
Fam168a |
G |
T |
7: 100,483,391 (GRCm39) |
|
probably null |
Het |
Fat3 |
G |
A |
9: 15,836,310 (GRCm39) |
R4065W |
possibly damaging |
Het |
Gm5431 |
T |
A |
11: 48,779,536 (GRCm39) |
N740I |
probably benign |
Het |
Gm5900 |
T |
A |
7: 104,599,571 (GRCm39) |
|
noncoding transcript |
Het |
Gpi1 |
A |
G |
7: 33,905,348 (GRCm39) |
S359P |
probably damaging |
Het |
Gpr156 |
A |
G |
16: 37,768,149 (GRCm39) |
R22G |
probably benign |
Het |
Greb1 |
A |
G |
12: 16,774,923 (GRCm39) |
V158A |
probably damaging |
Het |
Grin2c |
T |
A |
11: 115,141,894 (GRCm39) |
K842* |
probably null |
Het |
Gsta5 |
T |
A |
9: 78,202,089 (GRCm39) |
M1K |
probably null |
Het |
Hnf4a |
T |
A |
2: 163,408,161 (GRCm39) |
L329Q |
probably damaging |
Het |
Hsp90ab1 |
A |
G |
17: 45,880,267 (GRCm39) |
L92P |
probably damaging |
Het |
Ido1 |
T |
A |
8: 25,074,501 (GRCm39) |
R290* |
probably null |
Het |
Ifnlr1 |
G |
T |
4: 135,432,559 (GRCm39) |
D332Y |
probably damaging |
Het |
Ift172 |
T |
C |
5: 31,420,312 (GRCm39) |
N1108S |
probably benign |
Het |
Igkv3-9 |
T |
A |
6: 70,565,728 (GRCm39) |
M109K |
probably benign |
Het |
Igsf10 |
T |
C |
3: 59,239,287 (GRCm39) |
D298G |
probably damaging |
Het |
Iqck |
T |
G |
7: 118,475,505 (GRCm39) |
M98R |
probably benign |
Het |
Klk1b1 |
T |
C |
7: 43,618,803 (GRCm39) |
V60A |
probably damaging |
Het |
Krtap1-3 |
C |
T |
11: 99,481,653 (GRCm39) |
E165K |
unknown |
Het |
Lair1 |
A |
G |
7: 4,013,782 (GRCm39) |
L155P |
probably damaging |
Het |
Maco1 |
A |
G |
4: 134,531,699 (GRCm39) |
S657P |
probably damaging |
Het |
Mast4 |
G |
T |
13: 102,990,350 (GRCm39) |
S57Y |
probably damaging |
Het |
Mical3 |
T |
C |
6: 121,011,118 (GRCm39) |
H360R |
probably damaging |
Het |
Muc5b |
A |
T |
7: 141,412,798 (GRCm39) |
N1915Y |
unknown |
Het |
Myh1 |
A |
G |
11: 67,096,423 (GRCm39) |
I301V |
probably benign |
Het |
Nck2 |
T |
A |
1: 43,593,393 (GRCm39) |
V200E |
probably damaging |
Het |
Odad4 |
T |
G |
11: 100,444,361 (GRCm39) |
L222R |
probably damaging |
Het |
Or2y1b |
T |
G |
11: 49,209,048 (GRCm39) |
L225R |
probably damaging |
Het |
Or4b12 |
T |
C |
2: 90,096,030 (GRCm39) |
Y248C |
possibly damaging |
Het |
Or4c109 |
T |
G |
2: 88,817,775 (GRCm39) |
Y257S |
probably damaging |
Het |
Or4f60 |
T |
A |
2: 111,902,837 (GRCm39) |
L30F |
probably benign |
Het |
Or4k38 |
C |
T |
2: 111,166,076 (GRCm39) |
V116I |
probably damaging |
Het |
Or52n2c |
G |
A |
7: 104,574,894 (GRCm39) |
H26Y |
probably benign |
Het |
Or5b101 |
T |
A |
19: 13,005,058 (GRCm39) |
I212F |
probably damaging |
Het |
Or8b12i |
A |
G |
9: 20,082,525 (GRCm39) |
L114P |
probably damaging |
Het |
Otoa |
C |
T |
7: 120,759,695 (GRCm39) |
T1099I |
probably benign |
Het |
Pask |
T |
A |
1: 93,258,485 (GRCm39) |
I288F |
possibly damaging |
Het |
Pcnx4 |
T |
C |
12: 72,613,746 (GRCm39) |
W564R |
probably damaging |
Het |
Pip4p1 |
A |
T |
14: 51,167,115 (GRCm39) |
Y129* |
probably null |
Het |
Pitpnm2 |
T |
C |
5: 124,274,389 (GRCm39) |
E240G |
probably damaging |
Het |
Ppp1r16b |
A |
G |
2: 158,603,383 (GRCm39) |
Y436C |
possibly damaging |
Het |
Pramel27 |
G |
A |
4: 143,578,561 (GRCm39) |
V274I |
probably benign |
Het |
Prkca |
T |
C |
11: 107,870,032 (GRCm39) |
Y37C |
probably damaging |
Het |
Rad18 |
T |
G |
6: 112,652,883 (GRCm39) |
H238P |
possibly damaging |
Het |
Rap1b |
T |
A |
10: 117,654,444 (GRCm39) |
Q1L |
probably damaging |
Het |
Rgs9 |
T |
C |
11: 109,159,798 (GRCm39) |
Y178C |
probably benign |
Het |
Rpl3l |
A |
T |
17: 24,951,360 (GRCm39) |
D87V |
possibly damaging |
Het |
Scrn2 |
T |
C |
11: 96,923,992 (GRCm39) |
V292A |
possibly damaging |
Het |
Sdad1 |
A |
G |
5: 92,453,684 (GRCm39) |
Y35H |
probably benign |
Het |
Sez6l2 |
T |
C |
7: 126,552,944 (GRCm39) |
S177P |
probably benign |
Het |
Sh3bp1 |
C |
T |
15: 78,795,706 (GRCm39) |
P612S |
probably damaging |
Het |
Shank1 |
T |
C |
7: 44,001,148 (GRCm39) |
S956P |
unknown |
Het |
Shank1 |
G |
A |
7: 44,001,547 (GRCm39) |
A1089T |
unknown |
Het |
Spata22 |
C |
T |
11: 73,236,593 (GRCm39) |
P300S |
probably damaging |
Het |
Sstr2 |
A |
T |
11: 113,515,749 (GRCm39) |
I223F |
probably damaging |
Het |
Stom |
C |
T |
2: 35,210,354 (GRCm39) |
A217T |
probably damaging |
Het |
Stpg1 |
T |
C |
4: 135,263,960 (GRCm39) |
V341A |
probably benign |
Het |
Tagap |
A |
G |
17: 8,147,586 (GRCm39) |
T99A |
probably benign |
Het |
Tas1r2 |
A |
G |
4: 139,387,162 (GRCm39) |
N207S |
probably damaging |
Het |
Thbs2 |
A |
G |
17: 14,906,105 (GRCm39) |
V265A |
probably benign |
Het |
Thyn1 |
A |
G |
9: 26,911,316 (GRCm39) |
R3G |
possibly damaging |
Het |
Tia1 |
T |
A |
6: 86,401,312 (GRCm39) |
|
probably null |
Het |
Tktl2 |
A |
G |
8: 66,965,504 (GRCm39) |
E354G |
probably benign |
Het |
Tmc8 |
A |
G |
11: 117,683,511 (GRCm39) |
T689A |
possibly damaging |
Het |
Tmem11 |
A |
T |
11: 60,755,807 (GRCm39) |
|
probably null |
Het |
Tnik |
T |
C |
3: 28,722,064 (GRCm39) |
V1310A |
probably damaging |
Het |
Trappc10 |
A |
G |
10: 78,047,357 (GRCm39) |
S380P |
possibly damaging |
Het |
Trim8 |
C |
T |
19: 46,503,734 (GRCm39) |
P429S |
probably benign |
Het |
Ttn |
C |
A |
2: 76,687,756 (GRCm39) |
|
probably benign |
Het |
Ulk2 |
T |
C |
11: 61,678,340 (GRCm39) |
Y793C |
probably benign |
Het |
Vill |
G |
A |
9: 118,899,370 (GRCm39) |
V337M |
possibly damaging |
Het |
Vps53 |
C |
A |
11: 75,957,661 (GRCm39) |
V364F |
possibly damaging |
Het |
Zan |
A |
T |
5: 137,454,848 (GRCm39) |
I1396N |
unknown |
Het |
Zfa-ps |
A |
C |
10: 52,420,339 (GRCm39) |
|
noncoding transcript |
Het |
Zfp426 |
T |
C |
9: 20,381,977 (GRCm39) |
T337A |
possibly damaging |
Het |
Zfp536 |
T |
C |
7: 37,267,403 (GRCm39) |
E671G |
possibly damaging |
Het |
Zfp985 |
A |
G |
4: 147,667,443 (GRCm39) |
T104A |
possibly damaging |
Het |
|
Other mutations in Shprh |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00492:Shprh
|
APN |
10 |
11,063,902 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00583:Shprh
|
APN |
10 |
11,063,764 (GRCm39) |
missense |
probably benign |
0.37 |
IGL00684:Shprh
|
APN |
10 |
11,038,781 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01295:Shprh
|
APN |
10 |
11,059,612 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01387:Shprh
|
APN |
10 |
11,045,998 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01635:Shprh
|
APN |
10 |
11,045,763 (GRCm39) |
nonsense |
probably null |
|
IGL01833:Shprh
|
APN |
10 |
11,066,806 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02013:Shprh
|
APN |
10 |
11,057,246 (GRCm39) |
splice site |
probably benign |
|
IGL02502:Shprh
|
APN |
10 |
11,070,101 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02819:Shprh
|
APN |
10 |
11,030,509 (GRCm39) |
missense |
possibly damaging |
0.93 |
PIT4581001:Shprh
|
UTSW |
10 |
11,068,238 (GRCm39) |
frame shift |
probably null |
|
R0010:Shprh
|
UTSW |
10 |
11,027,675 (GRCm39) |
missense |
probably benign |
|
R0010:Shprh
|
UTSW |
10 |
11,027,675 (GRCm39) |
missense |
probably benign |
|
R0053:Shprh
|
UTSW |
10 |
11,070,116 (GRCm39) |
splice site |
probably null |
|
R0053:Shprh
|
UTSW |
10 |
11,070,116 (GRCm39) |
splice site |
probably null |
|
R0255:Shprh
|
UTSW |
10 |
11,062,135 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0325:Shprh
|
UTSW |
10 |
11,045,853 (GRCm39) |
missense |
probably benign |
0.00 |
R0331:Shprh
|
UTSW |
10 |
11,069,914 (GRCm39) |
splice site |
probably benign |
|
R0494:Shprh
|
UTSW |
10 |
11,032,935 (GRCm39) |
missense |
probably damaging |
1.00 |
R0532:Shprh
|
UTSW |
10 |
11,038,556 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0546:Shprh
|
UTSW |
10 |
11,059,631 (GRCm39) |
splice site |
probably benign |
|
R0574:Shprh
|
UTSW |
10 |
11,038,821 (GRCm39) |
unclassified |
probably benign |
|
R0605:Shprh
|
UTSW |
10 |
11,082,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R0662:Shprh
|
UTSW |
10 |
11,062,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R1148:Shprh
|
UTSW |
10 |
11,089,226 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1148:Shprh
|
UTSW |
10 |
11,089,226 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1263:Shprh
|
UTSW |
10 |
11,035,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R1588:Shprh
|
UTSW |
10 |
11,040,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R1638:Shprh
|
UTSW |
10 |
11,032,822 (GRCm39) |
missense |
probably benign |
|
R1830:Shprh
|
UTSW |
10 |
11,062,655 (GRCm39) |
splice site |
probably null |
|
R1898:Shprh
|
UTSW |
10 |
11,062,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R1903:Shprh
|
UTSW |
10 |
11,059,541 (GRCm39) |
nonsense |
probably null |
|
R2060:Shprh
|
UTSW |
10 |
11,027,864 (GRCm39) |
missense |
probably benign |
0.03 |
R2225:Shprh
|
UTSW |
10 |
11,037,979 (GRCm39) |
unclassified |
probably benign |
|
R2363:Shprh
|
UTSW |
10 |
11,047,697 (GRCm39) |
missense |
probably damaging |
1.00 |
R2891:Shprh
|
UTSW |
10 |
11,040,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R3077:Shprh
|
UTSW |
10 |
11,046,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R3150:Shprh
|
UTSW |
10 |
11,045,774 (GRCm39) |
missense |
probably damaging |
0.97 |
R3796:Shprh
|
UTSW |
10 |
11,054,501 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4196:Shprh
|
UTSW |
10 |
11,083,604 (GRCm39) |
utr 3 prime |
probably benign |
|
R4423:Shprh
|
UTSW |
10 |
11,062,262 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4488:Shprh
|
UTSW |
10 |
11,036,215 (GRCm39) |
missense |
probably benign |
0.17 |
R4748:Shprh
|
UTSW |
10 |
11,046,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R4768:Shprh
|
UTSW |
10 |
11,057,284 (GRCm39) |
missense |
probably damaging |
0.96 |
R4867:Shprh
|
UTSW |
10 |
11,040,301 (GRCm39) |
missense |
probably benign |
0.00 |
R4937:Shprh
|
UTSW |
10 |
11,032,863 (GRCm39) |
missense |
probably benign |
|
R5140:Shprh
|
UTSW |
10 |
11,030,449 (GRCm39) |
missense |
probably benign |
0.03 |
R5318:Shprh
|
UTSW |
10 |
11,042,301 (GRCm39) |
missense |
probably benign |
0.04 |
R5323:Shprh
|
UTSW |
10 |
11,046,041 (GRCm39) |
splice site |
probably null |
|
R5450:Shprh
|
UTSW |
10 |
11,088,074 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5872:Shprh
|
UTSW |
10 |
11,063,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R6030:Shprh
|
UTSW |
10 |
11,027,735 (GRCm39) |
missense |
probably benign |
0.37 |
R6030:Shprh
|
UTSW |
10 |
11,027,735 (GRCm39) |
missense |
probably benign |
0.37 |
R6392:Shprh
|
UTSW |
10 |
11,054,485 (GRCm39) |
nonsense |
probably null |
|
R6416:Shprh
|
UTSW |
10 |
11,043,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R6470:Shprh
|
UTSW |
10 |
11,047,681 (GRCm39) |
missense |
probably damaging |
0.98 |
R6513:Shprh
|
UTSW |
10 |
11,062,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R6530:Shprh
|
UTSW |
10 |
11,070,011 (GRCm39) |
missense |
probably benign |
0.02 |
R6678:Shprh
|
UTSW |
10 |
11,042,289 (GRCm39) |
missense |
probably benign |
0.16 |
R6757:Shprh
|
UTSW |
10 |
11,057,252 (GRCm39) |
splice site |
probably null |
|
R6971:Shprh
|
UTSW |
10 |
11,042,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R7158:Shprh
|
UTSW |
10 |
11,042,474 (GRCm39) |
missense |
probably damaging |
0.98 |
R7582:Shprh
|
UTSW |
10 |
11,040,449 (GRCm39) |
missense |
probably benign |
|
R7757:Shprh
|
UTSW |
10 |
11,037,924 (GRCm39) |
missense |
probably benign |
0.30 |
R7812:Shprh
|
UTSW |
10 |
11,027,735 (GRCm39) |
missense |
probably benign |
|
R7998:Shprh
|
UTSW |
10 |
11,061,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R8061:Shprh
|
UTSW |
10 |
11,088,077 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8082:Shprh
|
UTSW |
10 |
11,027,555 (GRCm39) |
missense |
probably benign |
0.22 |
R8116:Shprh
|
UTSW |
10 |
11,089,205 (GRCm39) |
missense |
probably damaging |
0.99 |
R8390:Shprh
|
UTSW |
10 |
11,063,727 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8445:Shprh
|
UTSW |
10 |
11,057,313 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8530:Shprh
|
UTSW |
10 |
11,027,678 (GRCm39) |
missense |
probably benign |
0.37 |
R8759:Shprh
|
UTSW |
10 |
11,032,908 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8937:Shprh
|
UTSW |
10 |
11,061,181 (GRCm39) |
missense |
possibly damaging |
0.60 |
R8995:Shprh
|
UTSW |
10 |
11,040,574 (GRCm39) |
nonsense |
probably null |
|
R9053:Shprh
|
UTSW |
10 |
11,030,446 (GRCm39) |
missense |
probably benign |
0.04 |
R9131:Shprh
|
UTSW |
10 |
11,038,589 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9176:Shprh
|
UTSW |
10 |
11,036,320 (GRCm39) |
missense |
probably benign |
0.02 |
R9391:Shprh
|
UTSW |
10 |
11,038,633 (GRCm39) |
missense |
probably benign |
0.05 |
R9423:Shprh
|
UTSW |
10 |
11,081,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R9563:Shprh
|
UTSW |
10 |
11,042,235 (GRCm39) |
nonsense |
probably null |
|
R9668:Shprh
|
UTSW |
10 |
11,082,076 (GRCm39) |
missense |
probably damaging |
0.97 |
R9709:Shprh
|
UTSW |
10 |
11,038,574 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9718:Shprh
|
UTSW |
10 |
11,089,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R9750:Shprh
|
UTSW |
10 |
11,040,204 (GRCm39) |
missense |
probably damaging |
0.98 |
RF012:Shprh
|
UTSW |
10 |
11,040,585 (GRCm39) |
missense |
probably benign |
0.02 |
V8831:Shprh
|
UTSW |
10 |
11,062,606 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Shprh
|
UTSW |
10 |
11,062,191 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Shprh
|
UTSW |
10 |
11,040,297 (GRCm39) |
missense |
probably benign |
|
Z1177:Shprh
|
UTSW |
10 |
11,027,506 (GRCm39) |
frame shift |
probably null |
|
|
Predicted Primers |
PCR Primer
(F):5'- AGAAACACGGCTTCTTACAGC -3'
(R):5'- GTCATACACACAGATATCCAAGTAGTC -3'
Sequencing Primer
(F):5'- ATAGTGAAGATGGGCGTC -3'
(R):5'- GTAGTCCATACAAAACTATCATCCAG -3'
|
Posted On |
2014-12-04 |