Incidental Mutation 'R6398:Rsf1'
ID |
516068 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Rsf1
|
Ensembl Gene |
ENSMUSG00000035623 |
Gene Name |
remodeling and spacing factor 1 |
Synonyms |
p325, Hbxap, C030033M12Rik, 4832420A03Rik, XAP8 |
MMRRC Submission |
044381-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R6398 (G1)
|
Quality Score |
217.554 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
97579889-97692778 bp(+) (GRCm38) |
Type of Mutation |
unclassified |
DNA Base Change (assembly) |
GCG to GCGACGGCGACG
at 97579907 bp (GRCm38)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000137067
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042627]
[ENSMUST00000072725]
[ENSMUST00000107153]
[ENSMUST00000124552]
[ENSMUST00000126085]
[ENSMUST00000127891]
[ENSMUST00000135998]
[ENSMUST00000136757]
[ENSMUST00000138060]
[ENSMUST00000144858]
[ENSMUST00000154853]
[ENSMUST00000178078]
[ENSMUST00000151840]
[ENSMUST00000154779]
[ENSMUST00000146605]
|
AlphaFold |
E9PWW9 |
Predicted Effect |
unknown
Transcript: ENSMUST00000042399
|
SMART Domains |
Protein: ENSMUSP00000037409 Gene: ENSMUSG00000035623
Domain | Start | End | E-Value | Type |
low complexity region
|
1 |
17 |
N/A |
INTRINSIC |
low complexity region
|
40 |
53 |
N/A |
INTRINSIC |
Pfam:WHIM1
|
103 |
153 |
9.3e-11 |
PFAM |
Pfam:WHIM2
|
155 |
187 |
7.2e-10 |
PFAM |
low complexity region
|
236 |
246 |
N/A |
INTRINSIC |
low complexity region
|
299 |
311 |
N/A |
INTRINSIC |
low complexity region
|
758 |
773 |
N/A |
INTRINSIC |
low complexity region
|
860 |
874 |
N/A |
INTRINSIC |
low complexity region
|
878 |
887 |
N/A |
INTRINSIC |
PHD
|
896 |
942 |
1.57e-11 |
SMART |
low complexity region
|
960 |
974 |
N/A |
INTRINSIC |
low complexity region
|
986 |
1008 |
N/A |
INTRINSIC |
low complexity region
|
1026 |
1045 |
N/A |
INTRINSIC |
low complexity region
|
1087 |
1111 |
N/A |
INTRINSIC |
low complexity region
|
1125 |
1143 |
N/A |
INTRINSIC |
low complexity region
|
1148 |
1167 |
N/A |
INTRINSIC |
low complexity region
|
1175 |
1205 |
N/A |
INTRINSIC |
low complexity region
|
1207 |
1213 |
N/A |
INTRINSIC |
low complexity region
|
1249 |
1263 |
N/A |
INTRINSIC |
low complexity region
|
1283 |
1295 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000042627
|
SMART Domains |
Protein: ENSMUSP00000035883 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
Pfam:DUF498
|
68 |
115 |
1.5e-12 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000072725
|
SMART Domains |
Protein: ENSMUSP00000072508 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
Pfam:DUF498
|
68 |
115 |
1.5e-12 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000107153
|
SMART Domains |
Protein: ENSMUSP00000102771 Gene: ENSMUSG00000035623
Domain | Start | End | E-Value | Type |
low complexity region
|
25 |
38 |
N/A |
INTRINSIC |
Pfam:WHIM1
|
88 |
138 |
2.2e-10 |
PFAM |
Pfam:WHIM2
|
140 |
172 |
9.4e-8 |
PFAM |
Pfam:WHIM3
|
178 |
398 |
2.5e-27 |
PFAM |
low complexity region
|
743 |
758 |
N/A |
INTRINSIC |
low complexity region
|
845 |
859 |
N/A |
INTRINSIC |
low complexity region
|
863 |
872 |
N/A |
INTRINSIC |
PHD
|
881 |
927 |
1.57e-11 |
SMART |
low complexity region
|
945 |
959 |
N/A |
INTRINSIC |
low complexity region
|
971 |
993 |
N/A |
INTRINSIC |
low complexity region
|
1011 |
1030 |
N/A |
INTRINSIC |
low complexity region
|
1072 |
1096 |
N/A |
INTRINSIC |
low complexity region
|
1110 |
1128 |
N/A |
INTRINSIC |
low complexity region
|
1133 |
1152 |
N/A |
INTRINSIC |
low complexity region
|
1160 |
1190 |
N/A |
INTRINSIC |
low complexity region
|
1192 |
1198 |
N/A |
INTRINSIC |
low complexity region
|
1234 |
1248 |
N/A |
INTRINSIC |
low complexity region
|
1268 |
1280 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000124552
|
SMART Domains |
Protein: ENSMUSP00000120661 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
Pfam:DUF498
|
2 |
49 |
8.5e-14 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000126085
|
SMART Domains |
Protein: ENSMUSP00000120089 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
15 |
N/A |
INTRINSIC |
SCOP:d1uroa_
|
21 |
60 |
2e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000127891
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000135998
|
SMART Domains |
Protein: ENSMUSP00000118391 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
Pfam:DUF498
|
34 |
128 |
4.8e-21 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000136757
|
SMART Domains |
Protein: ENSMUSP00000121940 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
Pfam:DUF498
|
6 |
119 |
2.1e-28 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000138060
|
SMART Domains |
Protein: ENSMUSP00000116214 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
Pfam:DUF498
|
40 |
87 |
1.7e-12 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000140805
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000144858
|
SMART Domains |
Protein: ENSMUSP00000117205 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
Pfam:DUF498
|
11 |
65 |
3.8e-13 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000205536
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000205430
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156060
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000154853
|
SMART Domains |
Protein: ENSMUSP00000115672 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
Pfam:DUF498
|
34 |
147 |
9.4e-28 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000178078
|
SMART Domains |
Protein: ENSMUSP00000137067 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
Pfam:DUF498
|
34 |
147 |
2.7e-24 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000151840
|
SMART Domains |
Protein: ENSMUSP00000115852 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
20 |
N/A |
INTRINSIC |
PDB:2Q4Q|B
|
31 |
75 |
5e-23 |
PDB |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000154779
|
SMART Domains |
Protein: ENSMUSP00000120195 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
low complexity region
|
6 |
15 |
N/A |
INTRINSIC |
transmembrane domain
|
30 |
49 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000146605
|
SMART Domains |
Protein: ENSMUSP00000117571 Gene: ENSMUSG00000035642
Domain | Start | End | E-Value | Type |
Pfam:DUF498
|
23 |
136 |
3.4e-28 |
PFAM |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 99.9%
- 10x: 99.4%
- 20x: 97.9%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a nuclear protein that interacts with hepatitis B virus X protein (HBX) and facilitates transcription of hepatitis B virus genes by the HBX transcription activator, suggesting a role for this interaction in the virus life cycle. This protein also interacts with SNF2H protein to form the RSF chromatin-remodeling complex, where the SNF2H subunit functions as the nucleosome-dependent ATPase, and this protein as the histone chaperone. [provided by RefSeq, Sep 2011]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ago1 |
T |
A |
4: 126,448,808 |
Q514L |
probably benign |
Het |
Alpi |
G |
C |
1: 87,099,462 |
T365S |
probably damaging |
Het |
Cbx4 |
A |
T |
11: 119,081,082 |
V489E |
probably damaging |
Het |
Ccdc162 |
T |
C |
10: 41,627,149 |
D999G |
probably damaging |
Het |
Clspn |
A |
G |
4: 126,563,947 |
E88G |
probably damaging |
Het |
D6Ertd527e |
C |
G |
6: 87,111,524 |
T223S |
unknown |
Het |
Ddx1 |
A |
T |
12: 13,245,720 |
I33N |
probably damaging |
Het |
Diaph3 |
G |
A |
14: 86,866,486 |
L821F |
probably damaging |
Het |
Duox2 |
C |
T |
2: 122,296,370 |
M221I |
probably benign |
Het |
Gm15130 |
A |
T |
2: 111,135,442 |
M154K |
unknown |
Het |
Gm3233 |
G |
T |
10: 77,759,415 |
|
probably benign |
Het |
Heg1 |
A |
C |
16: 33,766,775 |
I1327L |
probably damaging |
Het |
Ifnar1 |
G |
A |
16: 91,505,415 |
|
probably null |
Het |
Itpr1 |
C |
T |
6: 108,505,903 |
L2310F |
probably damaging |
Het |
Olfr1450 |
T |
C |
19: 12,954,317 |
S243P |
probably damaging |
Het |
Pcdhb7 |
A |
G |
18: 37,343,434 |
N541S |
possibly damaging |
Het |
Prelp |
A |
G |
1: 133,914,741 |
L222P |
probably damaging |
Het |
Prl8a8 |
A |
G |
13: 27,508,429 |
I193T |
probably damaging |
Het |
Prpf4b |
G |
T |
13: 34,900,371 |
R914L |
probably damaging |
Het |
Ptbp2 |
G |
C |
3: 119,720,835 |
Q448E |
probably benign |
Het |
Slc9a9 |
A |
T |
9: 94,670,227 |
M56L |
probably benign |
Het |
Slfn4 |
A |
G |
11: 83,187,174 |
I263V |
possibly damaging |
Het |
Taar2 |
A |
G |
10: 23,941,279 |
N239S |
probably benign |
Het |
Trrap |
T |
A |
5: 144,790,870 |
I467N |
possibly damaging |
Het |
Ttc28 |
T |
C |
5: 111,276,276 |
Y1439H |
probably damaging |
Het |
Usp34 |
A |
G |
11: 23,488,666 |
I3409M |
probably benign |
Het |
Zbbx |
G |
T |
3: 75,078,565 |
N388K |
probably damaging |
Het |
Znhit2 |
A |
G |
19: 6,062,257 |
N344S |
probably damaging |
Het |
|
Other mutations in Rsf1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00650:Rsf1
|
APN |
7 |
97681889 |
critical splice donor site |
probably null |
0.00 |
IGL01160:Rsf1
|
APN |
7 |
97685584 |
missense |
probably damaging |
1.00 |
IGL01780:Rsf1
|
APN |
7 |
97664770 |
critical splice donor site |
probably benign |
0.00 |
IGL01960:Rsf1
|
APN |
7 |
97661575 |
missense |
probably benign |
0.00 |
IGL02487:Rsf1
|
APN |
7 |
97639491 |
missense |
probably damaging |
0.99 |
IGL02814:Rsf1
|
APN |
7 |
97661227 |
missense |
probably damaging |
1.00 |
IGL02972:Rsf1
|
APN |
7 |
97661326 |
missense |
probably benign |
0.35 |
IGL03176:Rsf1
|
APN |
7 |
97679150 |
splice site |
probably benign |
|
IGL03256:Rsf1
|
APN |
7 |
97679004 |
missense |
possibly damaging |
0.82 |
BB011:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
BB014:Rsf1
|
UTSW |
7 |
97579924 |
unclassified |
probably benign |
|
BB018:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
FR4976:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
G1Funyon:Rsf1
|
UTSW |
7 |
97661925 |
missense |
|
|
P0023:Rsf1
|
UTSW |
7 |
97662271 |
missense |
probably damaging |
1.00 |
R0144:Rsf1
|
UTSW |
7 |
97636407 |
missense |
probably damaging |
1.00 |
R0380:Rsf1
|
UTSW |
7 |
97579905 |
unclassified |
probably benign |
|
R0392:Rsf1
|
UTSW |
7 |
97679005 |
missense |
probably benign |
0.00 |
R0422:Rsf1
|
UTSW |
7 |
97680817 |
missense |
probably benign |
0.04 |
R0584:Rsf1
|
UTSW |
7 |
97662128 |
missense |
possibly damaging |
0.60 |
R0636:Rsf1
|
UTSW |
7 |
97662019 |
missense |
possibly damaging |
0.74 |
R0729:Rsf1
|
UTSW |
7 |
97679027 |
missense |
probably damaging |
1.00 |
R0755:Rsf1
|
UTSW |
7 |
97579967 |
missense |
probably damaging |
1.00 |
R0947:Rsf1
|
UTSW |
7 |
97669778 |
missense |
probably damaging |
1.00 |
R1278:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R1376:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R1376:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R1498:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R1525:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R1534:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R1582:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R1591:Rsf1
|
UTSW |
7 |
97639313 |
nonsense |
probably null |
|
R1676:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R1695:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R1710:Rsf1
|
UTSW |
7 |
97662349 |
missense |
possibly damaging |
0.50 |
R1722:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R1764:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R1815:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R1815:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R1815:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R1823:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R1864:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R1884:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R1897:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R1915:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R1928:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R1958:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R1962:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R1962:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R1996:Rsf1
|
UTSW |
7 |
97664632 |
missense |
probably damaging |
1.00 |
R1999:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R2021:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R2022:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R2046:Rsf1
|
UTSW |
7 |
97661677 |
missense |
probably benign |
0.00 |
R2048:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R2093:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R2103:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R2137:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R2167:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R2179:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R2191:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R2207:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R2211:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R2241:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R2264:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R2283:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R2297:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R2307:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R2419:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R2442:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R2696:Rsf1
|
UTSW |
7 |
97579933 |
unclassified |
probably benign |
|
R2764:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R2939:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R2965:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R2972:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R3008:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R3013:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R3026:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R3110:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R3147:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R3427:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R3610:Rsf1
|
UTSW |
7 |
97579904 |
start codon destroyed |
probably null |
|
R3624:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R3753:Rsf1
|
UTSW |
7 |
97662152 |
missense |
probably benign |
0.00 |
R3759:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R3780:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R3794:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R3889:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R3925:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R3964:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R4037:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R4057:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R4057:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R4084:Rsf1
|
UTSW |
7 |
97579919 |
unclassified |
probably benign |
|
R4240:Rsf1
|
UTSW |
7 |
97579935 |
unclassified |
probably benign |
|
R4303:Rsf1
|
UTSW |
7 |
97579920 |
unclassified |
probably benign |
|
R4383:Rsf1
|
UTSW |
7 |
97685476 |
missense |
possibly damaging |
0.86 |
R4492:Rsf1
|
UTSW |
7 |
97579923 |
unclassified |
probably benign |
|
R4525:Rsf1
|
UTSW |
7 |
97579926 |
unclassified |
probably benign |
|
R4530:Rsf1
|
UTSW |
7 |
97579923 |
unclassified |
probably benign |
|
R4543:Rsf1
|
UTSW |
7 |
97579922 |
unclassified |
probably benign |
|
R4629:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R4629:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R4632:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R4633:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R4652:Rsf1
|
UTSW |
7 |
97579919 |
unclassified |
probably benign |
|
R4675:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R4675:Rsf1
|
UTSW |
7 |
97579904 |
start codon destroyed |
probably null |
|
R4677:Rsf1
|
UTSW |
7 |
97680773 |
missense |
possibly damaging |
0.82 |
R4678:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R4769:Rsf1
|
UTSW |
7 |
97676222 |
missense |
probably damaging |
1.00 |
R4774:Rsf1
|
UTSW |
7 |
97579916 |
unclassified |
probably benign |
|
R4820:Rsf1
|
UTSW |
7 |
97579919 |
unclassified |
probably benign |
|
R4917:Rsf1
|
UTSW |
7 |
97662405 |
missense |
probably damaging |
1.00 |
R4918:Rsf1
|
UTSW |
7 |
97662405 |
missense |
probably damaging |
1.00 |
R4977:Rsf1
|
UTSW |
7 |
97579916 |
unclassified |
probably benign |
|
R4979:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R4994:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R4994:Rsf1
|
UTSW |
7 |
97579923 |
unclassified |
probably benign |
|
R5041:Rsf1
|
UTSW |
7 |
97579925 |
unclassified |
probably benign |
|
R5125:Rsf1
|
UTSW |
7 |
97661872 |
missense |
possibly damaging |
0.87 |
R5178:Rsf1
|
UTSW |
7 |
97661872 |
missense |
possibly damaging |
0.87 |
R5306:Rsf1
|
UTSW |
7 |
97579929 |
unclassified |
probably benign |
|
R5369:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R5371:Rsf1
|
UTSW |
7 |
97579913 |
unclassified |
probably benign |
|
R5403:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R5436:Rsf1
|
UTSW |
7 |
97579931 |
unclassified |
probably benign |
|
R5450:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R5532:Rsf1
|
UTSW |
7 |
97680695 |
missense |
probably damaging |
1.00 |
R5587:Rsf1
|
UTSW |
7 |
97662121 |
missense |
probably benign |
0.02 |
R5657:Rsf1
|
UTSW |
7 |
97579934 |
unclassified |
probably benign |
|
R5689:Rsf1
|
UTSW |
7 |
97579934 |
unclassified |
probably benign |
|
R5745:Rsf1
|
UTSW |
7 |
97579920 |
unclassified |
probably benign |
|
R5748:Rsf1
|
UTSW |
7 |
97579928 |
unclassified |
probably benign |
|
R5773:Rsf1
|
UTSW |
7 |
97579933 |
unclassified |
probably benign |
|
R5859:Rsf1
|
UTSW |
7 |
97685559 |
missense |
probably damaging |
1.00 |
R5938:Rsf1
|
UTSW |
7 |
97685559 |
missense |
probably damaging |
1.00 |
R6001:Rsf1
|
UTSW |
7 |
97579904 |
start codon destroyed |
probably null |
|
R6001:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R6001:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R6021:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6025:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6030:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6030:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6035:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6035:Rsf1
|
UTSW |
7 |
97662109 |
missense |
probably benign |
0.01 |
R6035:Rsf1
|
UTSW |
7 |
97662109 |
missense |
probably benign |
0.01 |
R6035:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6036:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6037:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6037:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6073:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6077:Rsf1
|
UTSW |
7 |
97579928 |
unclassified |
probably benign |
|
R6102:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6111:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R6126:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6128:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6130:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R6154:Rsf1
|
UTSW |
7 |
97579904 |
start codon destroyed |
probably null |
|
R6154:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R6165:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6166:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R6182:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R6189:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6200:Rsf1
|
UTSW |
7 |
97579925 |
unclassified |
probably benign |
|
R6210:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6212:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6214:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6215:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6216:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6232:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6235:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6242:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6243:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6244:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6268:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6269:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6273:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6275:Rsf1
|
UTSW |
7 |
97579923 |
unclassified |
probably benign |
|
R6286:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6291:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R6293:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6297:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R6302:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6309:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6312:Rsf1
|
UTSW |
7 |
97579904 |
start codon destroyed |
probably null |
|
R6324:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6343:Rsf1
|
UTSW |
7 |
97660917 |
missense |
probably benign |
0.30 |
R6346:Rsf1
|
UTSW |
7 |
97579904 |
start codon destroyed |
probably null |
|
R6356:Rsf1
|
UTSW |
7 |
97661934 |
missense |
probably benign |
|
R6370:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R6377:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6377:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6378:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6394:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6406:Rsf1
|
UTSW |
7 |
97579926 |
unclassified |
probably benign |
|
R6413:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R6443:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6453:Rsf1
|
UTSW |
7 |
97579917 |
unclassified |
probably benign |
|
R6471:Rsf1
|
UTSW |
7 |
97579914 |
unclassified |
probably benign |
|
R6473:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6497:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6505:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R6561:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6572:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6607:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6611:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6622:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R6626:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6636:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6647:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R6648:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6669:Rsf1
|
UTSW |
7 |
97579925 |
unclassified |
probably benign |
|
R6673:Rsf1
|
UTSW |
7 |
97579918 |
unclassified |
probably benign |
|
R6679:Rsf1
|
UTSW |
7 |
97579904 |
start codon destroyed |
probably null |
|
R6685:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6694:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6694:Rsf1
|
UTSW |
7 |
97579928 |
unclassified |
probably benign |
|
R6695:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6697:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6726:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R6739:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6747:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6751:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6771:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6773:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R6787:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6800:Rsf1
|
UTSW |
7 |
97579932 |
unclassified |
probably benign |
|
R6804:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6806:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6815:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6820:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6823:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6829:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6861:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6862:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6869:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6875:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R6889:Rsf1
|
UTSW |
7 |
97579925 |
unclassified |
probably benign |
|
R6897:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6960:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6963:Rsf1
|
UTSW |
7 |
97579910 |
unclassified |
probably benign |
|
R6967:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R6969:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R6977:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R6996:Rsf1
|
UTSW |
7 |
97579911 |
unclassified |
probably benign |
|
R7066:Rsf1
|
UTSW |
7 |
97579918 |
unclassified |
probably benign |
|
R7109:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R7127:Rsf1
|
UTSW |
7 |
97579914 |
unclassified |
probably benign |
|
R7138:Rsf1
|
UTSW |
7 |
97669795 |
missense |
|
|
R7214:Rsf1
|
UTSW |
7 |
97579929 |
unclassified |
probably benign |
|
R7217:Rsf1
|
UTSW |
7 |
97579932 |
unclassified |
probably benign |
|
R7238:Rsf1
|
UTSW |
7 |
97579921 |
unclassified |
probably benign |
|
R7246:Rsf1
|
UTSW |
7 |
97579922 |
unclassified |
probably benign |
|
R7253:Rsf1
|
UTSW |
7 |
97579915 |
unclassified |
probably benign |
|
R7294:Rsf1
|
UTSW |
7 |
97579920 |
unclassified |
probably benign |
|
R7305:Rsf1
|
UTSW |
7 |
97579918 |
unclassified |
probably benign |
|
R7309:Rsf1
|
UTSW |
7 |
97579911 |
unclassified |
probably benign |
|
R7352:Rsf1
|
UTSW |
7 |
97579926 |
unclassified |
probably benign |
|
R7380:Rsf1
|
UTSW |
7 |
97579915 |
unclassified |
probably benign |
|
R7393:Rsf1
|
UTSW |
7 |
97579917 |
unclassified |
probably benign |
|
R7395:Rsf1
|
UTSW |
7 |
97579926 |
unclassified |
probably benign |
|
R7411:Rsf1
|
UTSW |
7 |
97579932 |
unclassified |
probably benign |
|
R7413:Rsf1
|
UTSW |
7 |
97579921 |
unclassified |
probably benign |
|
R7481:Rsf1
|
UTSW |
7 |
97579917 |
unclassified |
probably benign |
|
R7538:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R7541:Rsf1
|
UTSW |
7 |
97579911 |
unclassified |
probably benign |
|
R7545:Rsf1
|
UTSW |
7 |
97579927 |
unclassified |
probably benign |
|
R7574:Rsf1
|
UTSW |
7 |
97661167 |
missense |
|
|
R7578:Rsf1
|
UTSW |
7 |
97579932 |
unclassified |
probably benign |
|
R7599:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R7630:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R7632:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R7710:Rsf1
|
UTSW |
7 |
97681834 |
missense |
|
|
R7711:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R7715:Rsf1
|
UTSW |
7 |
97579912 |
unclassified |
probably benign |
|
R7719:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R7722:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R7729:Rsf1
|
UTSW |
7 |
97579911 |
unclassified |
probably benign |
|
R7734:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R7743:Rsf1
|
UTSW |
7 |
97579932 |
unclassified |
probably benign |
|
R7761:Rsf1
|
UTSW |
7 |
97579920 |
unclassified |
probably benign |
|
R7764:Rsf1
|
UTSW |
7 |
97579927 |
unclassified |
probably benign |
|
R7797:Rsf1
|
UTSW |
7 |
97661485 |
missense |
|
|
R7802:Rsf1
|
UTSW |
7 |
97661772 |
missense |
|
|
R7806:Rsf1
|
UTSW |
7 |
97579920 |
unclassified |
probably benign |
|
R7821:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R7823:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R7824:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R7825:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R7826:Rsf1
|
UTSW |
7 |
97661161 |
unclassified |
probably benign |
|
R7841:Rsf1
|
UTSW |
7 |
97579904 |
start codon destroyed |
probably null |
|
R7854:Rsf1
|
UTSW |
7 |
97579924 |
unclassified |
probably benign |
|
R7862:Rsf1
|
UTSW |
7 |
97579923 |
unclassified |
probably benign |
|
R7893:Rsf1
|
UTSW |
7 |
97661958 |
missense |
|
|
R7923:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R7924:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R7927:Rsf1
|
UTSW |
7 |
97579924 |
unclassified |
probably benign |
|
R7931:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R7951:Rsf1
|
UTSW |
7 |
97579912 |
unclassified |
probably benign |
|
R7957:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R7960:Rsf1
|
UTSW |
7 |
97579917 |
unclassified |
probably benign |
|
R7979:Rsf1
|
UTSW |
7 |
97685713 |
missense |
|
|
R7982:Rsf1
|
UTSW |
7 |
97579932 |
unclassified |
probably benign |
|
R7991:Rsf1
|
UTSW |
7 |
97661333 |
missense |
|
|
R8028:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R8030:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R8042:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R8062:Rsf1
|
UTSW |
7 |
97677387 |
missense |
|
|
R8076:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R8117:Rsf1
|
UTSW |
7 |
97639257 |
splice site |
probably null |
|
R8132:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R8153:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R8155:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R8166:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R8197:Rsf1
|
UTSW |
7 |
97579914 |
unclassified |
probably benign |
|
R8235:Rsf1
|
UTSW |
7 |
97676254 |
utr 3 prime |
probably benign |
|
R8245:Rsf1
|
UTSW |
7 |
97579915 |
unclassified |
probably benign |
|
R8282:Rsf1
|
UTSW |
7 |
97579920 |
frame shift |
probably null |
|
R8301:Rsf1
|
UTSW |
7 |
97661925 |
missense |
|
|
R8315:Rsf1
|
UTSW |
7 |
97579923 |
unclassified |
probably benign |
|
R8343:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R8370:Rsf1
|
UTSW |
7 |
97579929 |
unclassified |
probably benign |
|
R8372:Rsf1
|
UTSW |
7 |
97662417 |
missense |
|
|
R8376:Rsf1
|
UTSW |
7 |
97579917 |
unclassified |
probably benign |
|
R8382:Rsf1
|
UTSW |
7 |
97579917 |
unclassified |
probably benign |
|
R8392:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R8410:Rsf1
|
UTSW |
7 |
97579917 |
unclassified |
probably benign |
|
R8443:Rsf1
|
UTSW |
7 |
97616896 |
missense |
|
|
R8502:Rsf1
|
UTSW |
7 |
97579914 |
unclassified |
probably benign |
|
R8529:Rsf1
|
UTSW |
7 |
97670867 |
utr 3 prime |
probably benign |
|
R8537:Rsf1
|
UTSW |
7 |
97579914 |
unclassified |
probably benign |
|
R8554:Rsf1
|
UTSW |
7 |
97579923 |
unclassified |
probably benign |
|
R8558:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R8735:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R8742:Rsf1
|
UTSW |
7 |
97579914 |
unclassified |
probably benign |
|
R8772:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R8862:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R8866:Rsf1
|
UTSW |
7 |
97579913 |
unclassified |
probably benign |
|
R8889:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R8889:Rsf1
|
UTSW |
7 |
97678964 |
missense |
|
|
R8891:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R8892:Rsf1
|
UTSW |
7 |
97678964 |
missense |
|
|
R8907:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R8907:Rsf1
|
UTSW |
7 |
97579918 |
unclassified |
probably benign |
|
R8913:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R8916:Rsf1
|
UTSW |
7 |
97579933 |
unclassified |
probably benign |
|
R8924:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R8940:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R8946:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R8947:Rsf1
|
UTSW |
7 |
97681852 |
unclassified |
probably benign |
|
R8951:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R8975:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R9033:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R9044:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R9060:Rsf1
|
UTSW |
7 |
97579923 |
unclassified |
probably benign |
|
R9066:Rsf1
|
UTSW |
7 |
97579911 |
unclassified |
probably benign |
|
R9079:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R9080:Rsf1
|
UTSW |
7 |
97579904 |
start codon destroyed |
probably null |
|
R9094:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R9096:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R9101:Rsf1
|
UTSW |
7 |
97579907 |
unclassified |
probably benign |
|
R9102:Rsf1
|
UTSW |
7 |
97579931 |
unclassified |
probably benign |
|
R9123:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R9125:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R9126:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R9128:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R9157:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R9159:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
R9161:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R9187:Rsf1
|
UTSW |
7 |
97579933 |
unclassified |
probably benign |
|
R9240:Rsf1
|
UTSW |
7 |
97579912 |
unclassified |
probably benign |
|
R9250:Rsf1
|
UTSW |
7 |
97579914 |
unclassified |
probably benign |
|
R9257:Rsf1
|
UTSW |
7 |
97685711 |
missense |
|
|
R9288:Rsf1
|
UTSW |
7 |
97579912 |
unclassified |
probably benign |
|
R9345:Rsf1
|
UTSW |
7 |
97579932 |
unclassified |
probably benign |
|
R9406:Rsf1
|
UTSW |
7 |
97579911 |
unclassified |
probably benign |
|
R9411:Rsf1
|
UTSW |
7 |
97579904 |
start codon destroyed |
probably null |
|
R9414:Rsf1
|
UTSW |
7 |
97664558 |
critical splice acceptor site |
probably null |
|
R9420:Rsf1
|
UTSW |
7 |
97579927 |
unclassified |
probably benign |
|
R9421:Rsf1
|
UTSW |
7 |
97579934 |
unclassified |
probably benign |
|
R9423:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R9427:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R9448:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R9452:Rsf1
|
UTSW |
7 |
97579926 |
unclassified |
probably benign |
|
R9454:Rsf1
|
UTSW |
7 |
97579923 |
unclassified |
probably benign |
|
R9467:Rsf1
|
UTSW |
7 |
97579913 |
unclassified |
probably benign |
|
R9468:Rsf1
|
UTSW |
7 |
97579920 |
unclassified |
probably benign |
|
R9483:Rsf1
|
UTSW |
7 |
97579930 |
unclassified |
probably benign |
|
R9488:Rsf1
|
UTSW |
7 |
97579922 |
unclassified |
probably benign |
|
R9502:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R9507:Rsf1
|
UTSW |
7 |
97579934 |
unclassified |
probably benign |
|
R9509:Rsf1
|
UTSW |
7 |
97579920 |
unclassified |
probably benign |
|
R9519:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R9526:Rsf1
|
UTSW |
7 |
97579932 |
unclassified |
probably benign |
|
R9537:Rsf1
|
UTSW |
7 |
97579914 |
unclassified |
probably benign |
|
R9581:Rsf1
|
UTSW |
7 |
97579918 |
unclassified |
probably benign |
|
R9590:Rsf1
|
UTSW |
7 |
97579911 |
unclassified |
probably benign |
|
R9592:Rsf1
|
UTSW |
7 |
97579911 |
unclassified |
probably benign |
|
R9618:Rsf1
|
UTSW |
7 |
97579909 |
unclassified |
probably benign |
|
R9630:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R9685:Rsf1
|
UTSW |
7 |
97579932 |
unclassified |
probably benign |
|
R9716:Rsf1
|
UTSW |
7 |
97579932 |
unclassified |
probably benign |
|
R9748:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
R9774:Rsf1
|
UTSW |
7 |
97579931 |
unclassified |
probably benign |
|
R9795:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
R9802:Rsf1
|
UTSW |
7 |
97579906 |
unclassified |
probably benign |
|
RF034:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
RF036:Rsf1
|
UTSW |
7 |
97579908 |
unclassified |
probably benign |
|
X0025:Rsf1
|
UTSW |
7 |
97636444 |
missense |
probably damaging |
1.00 |
X0028:Rsf1
|
UTSW |
7 |
97660824 |
nonsense |
probably null |
|
Y4335:Rsf1
|
UTSW |
7 |
97579904 |
unclassified |
probably benign |
|
|
Predicted Primers |
PCR Primer
(F):5'- AGCCTTGAAGTCGTAGAGGG -3'
(R):5'- CAGGGTATCTATGGAGAGCTAAAGC -3'
Sequencing Primer
(F):5'- AGTTCTCGACTGCTCCGG -3'
(R):5'- TTCGGGCCGATCGCTTAC -3'
|
Posted On |
2018-05-04 |