Incidental Mutation 'IGL02338:Ahdc1'
ID |
288933 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Ahdc1
|
Ensembl Gene |
ENSMUSG00000037692 |
Gene Name |
AT hook, DNA binding motif, containing 1 |
Synonyms |
D030015G18Rik |
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.214)
|
Stock # |
IGL02338
|
Quality Score |
|
Status
|
|
Chromosome |
4 |
Chromosomal Location |
132738797-132805421 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
G to A
at 132789860 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Cysteine to Tyrosine
at position 367
(C367Y)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000101536
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000044521]
[ENSMUST00000105914]
[ENSMUST00000105915]
[ENSMUST00000105916]
|
AlphaFold |
Q6PAL7 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000044521
AA Change: C367Y
PolyPhen 2
Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000047113 Gene: ENSMUSG00000037692 AA Change: C367Y
Domain | Start | End | E-Value | Type |
low complexity region
|
25 |
48 |
N/A |
INTRINSIC |
low complexity region
|
61 |
75 |
N/A |
INTRINSIC |
low complexity region
|
207 |
234 |
N/A |
INTRINSIC |
low complexity region
|
259 |
279 |
N/A |
INTRINSIC |
low complexity region
|
284 |
303 |
N/A |
INTRINSIC |
low complexity region
|
327 |
341 |
N/A |
INTRINSIC |
low complexity region
|
369 |
379 |
N/A |
INTRINSIC |
AT_hook
|
395 |
407 |
2.04e2 |
SMART |
low complexity region
|
418 |
446 |
N/A |
INTRINSIC |
low complexity region
|
491 |
508 |
N/A |
INTRINSIC |
AT_hook
|
541 |
553 |
5.47e-1 |
SMART |
low complexity region
|
661 |
685 |
N/A |
INTRINSIC |
low complexity region
|
696 |
714 |
N/A |
INTRINSIC |
low complexity region
|
770 |
785 |
N/A |
INTRINSIC |
low complexity region
|
805 |
820 |
N/A |
INTRINSIC |
low complexity region
|
836 |
857 |
N/A |
INTRINSIC |
low complexity region
|
963 |
974 |
N/A |
INTRINSIC |
low complexity region
|
1003 |
1028 |
N/A |
INTRINSIC |
low complexity region
|
1072 |
1084 |
N/A |
INTRINSIC |
low complexity region
|
1153 |
1168 |
N/A |
INTRINSIC |
low complexity region
|
1180 |
1197 |
N/A |
INTRINSIC |
low complexity region
|
1243 |
1251 |
N/A |
INTRINSIC |
low complexity region
|
1257 |
1271 |
N/A |
INTRINSIC |
low complexity region
|
1422 |
1436 |
N/A |
INTRINSIC |
low complexity region
|
1513 |
1528 |
N/A |
INTRINSIC |
low complexity region
|
1566 |
1579 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000105914
AA Change: C367Y
PolyPhen 2
Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000101534 Gene: ENSMUSG00000037692 AA Change: C367Y
Domain | Start | End | E-Value | Type |
low complexity region
|
25 |
48 |
N/A |
INTRINSIC |
low complexity region
|
61 |
75 |
N/A |
INTRINSIC |
low complexity region
|
207 |
234 |
N/A |
INTRINSIC |
low complexity region
|
259 |
279 |
N/A |
INTRINSIC |
low complexity region
|
284 |
303 |
N/A |
INTRINSIC |
low complexity region
|
327 |
341 |
N/A |
INTRINSIC |
low complexity region
|
369 |
379 |
N/A |
INTRINSIC |
AT_hook
|
395 |
407 |
2.04e2 |
SMART |
low complexity region
|
418 |
446 |
N/A |
INTRINSIC |
low complexity region
|
491 |
508 |
N/A |
INTRINSIC |
AT_hook
|
541 |
553 |
5.47e-1 |
SMART |
Pfam:DUF4683
|
559 |
639 |
6.4e-15 |
PFAM |
low complexity region
|
661 |
685 |
N/A |
INTRINSIC |
low complexity region
|
696 |
714 |
N/A |
INTRINSIC |
low complexity region
|
770 |
785 |
N/A |
INTRINSIC |
low complexity region
|
805 |
820 |
N/A |
INTRINSIC |
low complexity region
|
836 |
857 |
N/A |
INTRINSIC |
low complexity region
|
963 |
974 |
N/A |
INTRINSIC |
low complexity region
|
1003 |
1028 |
N/A |
INTRINSIC |
low complexity region
|
1072 |
1084 |
N/A |
INTRINSIC |
low complexity region
|
1153 |
1168 |
N/A |
INTRINSIC |
low complexity region
|
1180 |
1197 |
N/A |
INTRINSIC |
low complexity region
|
1243 |
1251 |
N/A |
INTRINSIC |
low complexity region
|
1257 |
1271 |
N/A |
INTRINSIC |
low complexity region
|
1422 |
1436 |
N/A |
INTRINSIC |
low complexity region
|
1513 |
1528 |
N/A |
INTRINSIC |
low complexity region
|
1566 |
1579 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000105915
AA Change: C367Y
PolyPhen 2
Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000101535 Gene: ENSMUSG00000037692 AA Change: C367Y
Domain | Start | End | E-Value | Type |
low complexity region
|
25 |
48 |
N/A |
INTRINSIC |
low complexity region
|
61 |
75 |
N/A |
INTRINSIC |
low complexity region
|
207 |
234 |
N/A |
INTRINSIC |
low complexity region
|
259 |
279 |
N/A |
INTRINSIC |
low complexity region
|
284 |
303 |
N/A |
INTRINSIC |
low complexity region
|
327 |
341 |
N/A |
INTRINSIC |
low complexity region
|
369 |
379 |
N/A |
INTRINSIC |
AT_hook
|
395 |
407 |
2.04e2 |
SMART |
low complexity region
|
418 |
446 |
N/A |
INTRINSIC |
low complexity region
|
491 |
508 |
N/A |
INTRINSIC |
AT_hook
|
541 |
553 |
5.47e-1 |
SMART |
low complexity region
|
661 |
685 |
N/A |
INTRINSIC |
low complexity region
|
696 |
714 |
N/A |
INTRINSIC |
low complexity region
|
770 |
785 |
N/A |
INTRINSIC |
low complexity region
|
805 |
820 |
N/A |
INTRINSIC |
low complexity region
|
836 |
857 |
N/A |
INTRINSIC |
low complexity region
|
963 |
974 |
N/A |
INTRINSIC |
low complexity region
|
1003 |
1028 |
N/A |
INTRINSIC |
low complexity region
|
1072 |
1084 |
N/A |
INTRINSIC |
low complexity region
|
1153 |
1168 |
N/A |
INTRINSIC |
low complexity region
|
1180 |
1197 |
N/A |
INTRINSIC |
low complexity region
|
1243 |
1251 |
N/A |
INTRINSIC |
low complexity region
|
1257 |
1271 |
N/A |
INTRINSIC |
low complexity region
|
1422 |
1436 |
N/A |
INTRINSIC |
low complexity region
|
1513 |
1528 |
N/A |
INTRINSIC |
low complexity region
|
1566 |
1579 |
N/A |
INTRINSIC |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000105916
AA Change: C367Y
PolyPhen 2
Score 0.734 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000101536 Gene: ENSMUSG00000037692 AA Change: C367Y
Domain | Start | End | E-Value | Type |
low complexity region
|
25 |
48 |
N/A |
INTRINSIC |
low complexity region
|
61 |
75 |
N/A |
INTRINSIC |
low complexity region
|
207 |
234 |
N/A |
INTRINSIC |
low complexity region
|
259 |
279 |
N/A |
INTRINSIC |
low complexity region
|
284 |
303 |
N/A |
INTRINSIC |
low complexity region
|
327 |
341 |
N/A |
INTRINSIC |
low complexity region
|
369 |
379 |
N/A |
INTRINSIC |
AT_hook
|
395 |
407 |
2.04e2 |
SMART |
low complexity region
|
418 |
446 |
N/A |
INTRINSIC |
low complexity region
|
491 |
508 |
N/A |
INTRINSIC |
AT_hook
|
541 |
553 |
5.47e-1 |
SMART |
low complexity region
|
661 |
685 |
N/A |
INTRINSIC |
low complexity region
|
696 |
714 |
N/A |
INTRINSIC |
low complexity region
|
770 |
785 |
N/A |
INTRINSIC |
low complexity region
|
805 |
820 |
N/A |
INTRINSIC |
low complexity region
|
836 |
857 |
N/A |
INTRINSIC |
low complexity region
|
963 |
974 |
N/A |
INTRINSIC |
low complexity region
|
1003 |
1028 |
N/A |
INTRINSIC |
low complexity region
|
1072 |
1084 |
N/A |
INTRINSIC |
low complexity region
|
1153 |
1168 |
N/A |
INTRINSIC |
low complexity region
|
1180 |
1197 |
N/A |
INTRINSIC |
low complexity region
|
1243 |
1251 |
N/A |
INTRINSIC |
low complexity region
|
1257 |
1271 |
N/A |
INTRINSIC |
low complexity region
|
1422 |
1436 |
N/A |
INTRINSIC |
low complexity region
|
1513 |
1528 |
N/A |
INTRINSIC |
low complexity region
|
1566 |
1579 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000135548
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000142524
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000148518
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154482
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000154646
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000156677
|
Coding Region Coverage |
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein containing two AT-hooks, which likely function in DNA binding. Mutations in this gene were found in individuals with Xia-Gibbs syndrome. [provided by RefSeq, Jun 2014]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AI182371 |
T |
A |
2: 34,975,728 (GRCm39) |
I279L |
probably benign |
Het |
Ambp |
A |
T |
4: 63,061,934 (GRCm39) |
C332S |
probably damaging |
Het |
App |
T |
C |
16: 84,970,407 (GRCm39) |
T14A |
probably benign |
Het |
Asap1 |
A |
T |
15: 63,995,519 (GRCm39) |
|
probably null |
Het |
Aurka |
T |
C |
2: 172,201,778 (GRCm39) |
R242G |
probably benign |
Het |
BC034090 |
G |
A |
1: 155,093,217 (GRCm39) |
P747L |
probably damaging |
Het |
Bcl6b |
T |
C |
11: 70,119,918 (GRCm39) |
D23G |
probably damaging |
Het |
Cabp2 |
A |
C |
19: 4,134,154 (GRCm39) |
E42A |
possibly damaging |
Het |
Ccdc14 |
G |
A |
16: 34,542,173 (GRCm39) |
S557N |
probably benign |
Het |
Ccdc146 |
G |
T |
5: 21,524,604 (GRCm39) |
|
probably benign |
Het |
Cenpf |
T |
A |
1: 189,412,615 (GRCm39) |
Q216L |
probably damaging |
Het |
Ces1b |
G |
A |
8: 93,783,675 (GRCm39) |
P515L |
possibly damaging |
Het |
Col6a5 |
A |
T |
9: 105,755,829 (GRCm39) |
N2198K |
probably damaging |
Het |
Csmd2 |
A |
G |
4: 128,288,859 (GRCm39) |
S1133G |
possibly damaging |
Het |
Cspg5 |
G |
A |
9: 110,085,335 (GRCm39) |
R502H |
probably benign |
Het |
Cyp2g1 |
A |
G |
7: 26,514,229 (GRCm39) |
|
probably benign |
Het |
Dnajc27 |
A |
G |
12: 4,146,229 (GRCm39) |
Y86C |
probably damaging |
Het |
Dnm1 |
T |
C |
2: 32,202,783 (GRCm39) |
D715G |
probably damaging |
Het |
Dock1 |
G |
T |
7: 134,734,804 (GRCm39) |
L1317F |
possibly damaging |
Het |
Fanci |
T |
A |
7: 79,083,279 (GRCm39) |
Y727* |
probably null |
Het |
Fbxw20 |
T |
A |
9: 109,055,046 (GRCm39) |
T168S |
probably benign |
Het |
Folh1 |
A |
T |
7: 86,385,723 (GRCm39) |
|
probably benign |
Het |
Gas7 |
A |
T |
11: 67,573,557 (GRCm39) |
S379C |
probably damaging |
Het |
Gbp2b |
A |
G |
3: 142,309,987 (GRCm39) |
E259G |
probably benign |
Het |
Gm8325 |
T |
C |
3: 60,784,805 (GRCm39) |
|
noncoding transcript |
Het |
Gpr75 |
A |
T |
11: 30,841,730 (GRCm39) |
T212S |
probably benign |
Het |
Itgb4 |
A |
G |
11: 115,898,795 (GRCm39) |
T1711A |
probably damaging |
Het |
Ly75 |
T |
C |
2: 60,184,796 (GRCm39) |
S453G |
probably benign |
Het |
Maneal |
A |
G |
4: 124,754,276 (GRCm39) |
|
probably benign |
Het |
Marco |
A |
T |
1: 120,422,508 (GRCm39) |
I58N |
possibly damaging |
Het |
Mtcl1 |
A |
G |
17: 66,686,965 (GRCm39) |
I647T |
probably damaging |
Het |
Mtfr1l |
A |
T |
4: 134,258,054 (GRCm39) |
V56D |
probably damaging |
Het |
Npy1r |
G |
A |
8: 67,156,954 (GRCm39) |
V125I |
probably damaging |
Het |
Or1j19 |
C |
T |
2: 36,676,557 (GRCm39) |
Q7* |
probably null |
Het |
Or52n20 |
T |
C |
7: 104,320,888 (GRCm39) |
|
probably benign |
Het |
Or7g25 |
A |
G |
9: 19,159,960 (GRCm39) |
L245P |
probably damaging |
Het |
Osmr |
A |
T |
15: 6,867,210 (GRCm39) |
L362* |
probably null |
Het |
Pdlim2 |
T |
C |
14: 70,411,906 (GRCm39) |
D42G |
probably damaging |
Het |
Plcb4 |
T |
A |
2: 135,842,100 (GRCm39) |
I89N |
possibly damaging |
Het |
Prrc2b |
T |
A |
2: 32,104,047 (GRCm39) |
M1175K |
probably benign |
Het |
Pzp |
T |
A |
6: 128,463,133 (GRCm39) |
N1423I |
probably benign |
Het |
Retnla |
G |
A |
16: 48,664,561 (GRCm39) |
C105Y |
probably damaging |
Het |
Samd8 |
T |
A |
14: 21,825,544 (GRCm39) |
S167T |
possibly damaging |
Het |
Scg2 |
A |
G |
1: 79,414,210 (GRCm39) |
M171T |
possibly damaging |
Het |
Slc30a5 |
A |
G |
13: 100,939,941 (GRCm39) |
V658A |
probably damaging |
Het |
Slc41a2 |
T |
C |
10: 83,152,455 (GRCm39) |
R7G |
possibly damaging |
Het |
Slc44a2 |
A |
G |
9: 21,258,338 (GRCm39) |
T500A |
probably damaging |
Het |
Slc44a4 |
G |
T |
17: 35,142,786 (GRCm39) |
G396V |
possibly damaging |
Het |
Smarca5 |
A |
G |
8: 81,446,199 (GRCm39) |
|
probably benign |
Het |
St8sia6 |
T |
A |
2: 13,798,156 (GRCm39) |
R34W |
probably damaging |
Het |
Stk-ps2 |
T |
A |
1: 46,069,337 (GRCm39) |
|
noncoding transcript |
Het |
Stn1 |
T |
C |
19: 47,502,329 (GRCm39) |
Y235C |
probably damaging |
Het |
Tbx15 |
A |
G |
3: 99,259,800 (GRCm39) |
Y557C |
probably damaging |
Het |
Tgfbr1 |
G |
A |
4: 47,393,490 (GRCm39) |
|
probably null |
Het |
Thsd7b |
G |
T |
1: 129,523,508 (GRCm39) |
V181L |
probably damaging |
Het |
Tmpo |
G |
A |
10: 90,999,104 (GRCm39) |
R228C |
probably benign |
Het |
Trpm4 |
T |
G |
7: 44,976,422 (GRCm39) |
R51S |
probably damaging |
Het |
Vmn1r91 |
A |
T |
7: 19,835,671 (GRCm39) |
T197S |
probably damaging |
Het |
Vmn2r-ps158 |
T |
C |
7: 42,697,160 (GRCm39) |
I739T |
probably damaging |
Het |
Xrn1 |
A |
G |
9: 95,859,880 (GRCm39) |
D424G |
probably benign |
Het |
Yap1 |
A |
G |
9: 7,962,282 (GRCm39) |
|
probably null |
Het |
Zer1 |
T |
C |
2: 30,003,405 (GRCm39) |
D4G |
probably damaging |
Het |
Zfp462 |
A |
T |
4: 55,010,292 (GRCm39) |
I753F |
possibly damaging |
Het |
|
Other mutations in Ahdc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00946:Ahdc1
|
APN |
4 |
132,790,373 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02293:Ahdc1
|
APN |
4 |
132,792,929 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02828:Ahdc1
|
APN |
4 |
132,790,232 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02859:Ahdc1
|
APN |
4 |
132,790,004 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02859:Ahdc1
|
APN |
4 |
132,790,003 (GRCm39) |
missense |
possibly damaging |
0.53 |
IGL02901:Ahdc1
|
APN |
4 |
132,792,245 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03323:Ahdc1
|
APN |
4 |
132,792,739 (GRCm39) |
missense |
probably benign |
|
FR4304:Ahdc1
|
UTSW |
4 |
132,790,070 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Ahdc1
|
UTSW |
4 |
132,790,071 (GRCm39) |
small insertion |
probably benign |
|
FR4548:Ahdc1
|
UTSW |
4 |
132,790,068 (GRCm39) |
small insertion |
probably benign |
|
FR4737:Ahdc1
|
UTSW |
4 |
132,790,070 (GRCm39) |
small insertion |
probably benign |
|
R0325:Ahdc1
|
UTSW |
4 |
132,790,030 (GRCm39) |
missense |
unknown |
|
R0550:Ahdc1
|
UTSW |
4 |
132,790,348 (GRCm39) |
missense |
probably benign |
0.33 |
R0681:Ahdc1
|
UTSW |
4 |
132,792,827 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0683:Ahdc1
|
UTSW |
4 |
132,792,827 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0731:Ahdc1
|
UTSW |
4 |
132,790,262 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0751:Ahdc1
|
UTSW |
4 |
132,792,707 (GRCm39) |
missense |
probably benign |
0.02 |
R1137:Ahdc1
|
UTSW |
4 |
132,789,424 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1184:Ahdc1
|
UTSW |
4 |
132,792,707 (GRCm39) |
missense |
probably benign |
0.02 |
R1331:Ahdc1
|
UTSW |
4 |
132,791,002 (GRCm39) |
missense |
probably benign |
0.18 |
R1599:Ahdc1
|
UTSW |
4 |
132,792,247 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2202:Ahdc1
|
UTSW |
4 |
132,793,220 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2205:Ahdc1
|
UTSW |
4 |
132,793,220 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2261:Ahdc1
|
UTSW |
4 |
132,790,474 (GRCm39) |
missense |
unknown |
|
R2262:Ahdc1
|
UTSW |
4 |
132,790,474 (GRCm39) |
missense |
unknown |
|
R3683:Ahdc1
|
UTSW |
4 |
132,793,013 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3684:Ahdc1
|
UTSW |
4 |
132,793,013 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3685:Ahdc1
|
UTSW |
4 |
132,793,013 (GRCm39) |
missense |
possibly damaging |
0.96 |
R3713:Ahdc1
|
UTSW |
4 |
132,793,297 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4027:Ahdc1
|
UTSW |
4 |
132,791,476 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4807:Ahdc1
|
UTSW |
4 |
132,791,624 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4987:Ahdc1
|
UTSW |
4 |
132,791,631 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5126:Ahdc1
|
UTSW |
4 |
132,790,833 (GRCm39) |
missense |
probably benign |
0.18 |
R5276:Ahdc1
|
UTSW |
4 |
132,790,109 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5680:Ahdc1
|
UTSW |
4 |
132,792,907 (GRCm39) |
missense |
probably benign |
|
R5997:Ahdc1
|
UTSW |
4 |
132,791,206 (GRCm39) |
missense |
probably benign |
0.05 |
R6050:Ahdc1
|
UTSW |
4 |
132,793,202 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6271:Ahdc1
|
UTSW |
4 |
132,792,035 (GRCm39) |
missense |
possibly damaging |
0.73 |
R6410:Ahdc1
|
UTSW |
4 |
132,790,210 (GRCm39) |
missense |
probably damaging |
0.97 |
R6519:Ahdc1
|
UTSW |
4 |
132,792,079 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6970:Ahdc1
|
UTSW |
4 |
132,789,656 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7199:Ahdc1
|
UTSW |
4 |
132,791,935 (GRCm39) |
missense |
probably benign |
0.33 |
R7202:Ahdc1
|
UTSW |
4 |
132,789,198 (GRCm39) |
nonsense |
probably null |
|
R7576:Ahdc1
|
UTSW |
4 |
132,792,313 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7614:Ahdc1
|
UTSW |
4 |
132,790,825 (GRCm39) |
missense |
probably benign |
0.18 |
R7794:Ahdc1
|
UTSW |
4 |
132,791,289 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7875:Ahdc1
|
UTSW |
4 |
132,791,161 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8016:Ahdc1
|
UTSW |
4 |
132,790,226 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8295:Ahdc1
|
UTSW |
4 |
132,788,762 (GRCm39) |
start codon destroyed |
probably null |
0.53 |
R8332:Ahdc1
|
UTSW |
4 |
132,791,282 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8719:Ahdc1
|
UTSW |
4 |
132,791,533 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8725:Ahdc1
|
UTSW |
4 |
132,792,743 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8862:Ahdc1
|
UTSW |
4 |
132,791,129 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9158:Ahdc1
|
UTSW |
4 |
132,792,505 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9179:Ahdc1
|
UTSW |
4 |
132,788,929 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9362:Ahdc1
|
UTSW |
4 |
132,790,348 (GRCm39) |
missense |
probably benign |
0.33 |
R9428:Ahdc1
|
UTSW |
4 |
132,791,773 (GRCm39) |
missense |
possibly damaging |
0.93 |
RF017:Ahdc1
|
UTSW |
4 |
132,790,062 (GRCm39) |
small insertion |
probably benign |
|
RF020:Ahdc1
|
UTSW |
4 |
132,791,588 (GRCm39) |
missense |
possibly damaging |
0.96 |
T0722:Ahdc1
|
UTSW |
4 |
132,790,065 (GRCm39) |
small insertion |
probably benign |
|
T0975:Ahdc1
|
UTSW |
4 |
132,790,065 (GRCm39) |
small insertion |
probably benign |
|
|
Posted On |
2015-04-16 |