Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2010315B03Rik |
T |
C |
9: 124,058,078 (GRCm39) |
T14A |
|
Het |
2610008E11Rik |
T |
C |
10: 78,930,289 (GRCm39) |
N42D |
probably benign |
Het |
Ajm1 |
A |
G |
2: 25,469,246 (GRCm39) |
F222L |
probably benign |
Het |
Ankrd54 |
T |
A |
15: 78,939,641 (GRCm39) |
M183L |
|
Het |
Apob |
G |
A |
12: 8,056,435 (GRCm39) |
G1639D |
probably damaging |
Het |
B3gat2 |
A |
G |
1: 23,884,061 (GRCm39) |
T283A |
probably benign |
Het |
Bmpr2 |
T |
G |
1: 59,886,252 (GRCm39) |
S296R |
probably damaging |
Het |
Cand1 |
G |
A |
10: 119,042,721 (GRCm39) |
T1123I |
probably damaging |
Het |
Cc2d2a |
T |
C |
5: 43,869,781 (GRCm39) |
F943S |
probably damaging |
Het |
Ccdc40 |
T |
C |
11: 119,144,211 (GRCm39) |
I912T |
probably benign |
Het |
Cdkn2d |
G |
A |
9: 21,200,447 (GRCm39) |
S108L |
probably benign |
Het |
Cep295 |
G |
A |
9: 15,245,660 (GRCm39) |
T932I |
probably damaging |
Het |
Cntn5 |
A |
G |
9: 9,673,955 (GRCm39) |
S716P |
probably benign |
Het |
Col18a1 |
T |
C |
10: 76,895,808 (GRCm39) |
E903G |
probably benign |
Het |
Ctrc |
T |
A |
4: 141,565,972 (GRCm39) |
I229F |
probably damaging |
Het |
Cyb561d2 |
C |
T |
9: 107,418,771 (GRCm39) |
A18T |
probably benign |
Het |
Dnajb4 |
T |
A |
3: 151,899,089 (GRCm39) |
K46* |
probably null |
Het |
Dsc2 |
C |
T |
18: 20,165,331 (GRCm39) |
G881R |
possibly damaging |
Het |
Dsg1c |
C |
T |
18: 20,410,016 (GRCm39) |
H495Y |
probably benign |
Het |
Eif2b3 |
A |
G |
4: 116,879,414 (GRCm39) |
D18G |
probably damaging |
Het |
Enam |
A |
T |
5: 88,651,385 (GRCm39) |
I965L |
probably benign |
Het |
Fhod3 |
T |
A |
18: 25,248,910 (GRCm39) |
I1363K |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,855,245 (GRCm39) |
Y1918C |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,823,296 (GRCm39) |
I6343N |
possibly damaging |
Het |
Gpr45 |
G |
C |
1: 43,072,475 (GRCm39) |
V373L |
probably damaging |
Het |
Hdac2 |
G |
T |
10: 36,873,966 (GRCm39) |
Q365H |
probably damaging |
Het |
Hspa12b |
A |
G |
2: 130,980,389 (GRCm39) |
T103A |
possibly damaging |
Het |
Ifrd1 |
A |
T |
12: 40,262,350 (GRCm39) |
S287T |
probably benign |
Het |
Igkv6-15 |
G |
A |
6: 70,383,622 (GRCm39) |
P60S |
possibly damaging |
Het |
Ippk |
C |
T |
13: 49,599,818 (GRCm39) |
P226S |
|
Het |
Kctd19 |
T |
A |
8: 106,122,069 (GRCm39) |
D109V |
unknown |
Het |
Matn4 |
G |
A |
2: 164,234,851 (GRCm39) |
S540L |
probably damaging |
Het |
Matn4 |
T |
C |
2: 164,241,682 (GRCm39) |
K248E |
probably benign |
Het |
Muc16 |
G |
A |
9: 18,420,206 (GRCm39) |
Q97* |
probably null |
Het |
Mup18 |
A |
G |
4: 61,592,238 (GRCm39) |
C9R |
unknown |
Het |
Myh1 |
A |
G |
11: 67,113,031 (GRCm39) |
K1845R |
probably damaging |
Het |
Mysm1 |
G |
A |
4: 94,848,627 (GRCm39) |
R469* |
probably null |
Het |
Naip1 |
T |
C |
13: 100,563,509 (GRCm39) |
D552G |
possibly damaging |
Het |
Nrcam |
A |
G |
12: 44,618,371 (GRCm39) |
D787G |
probably benign |
Het |
Nrcam |
G |
A |
12: 44,645,365 (GRCm39) |
V1256I |
probably damaging |
Het |
Obscn |
G |
T |
11: 58,932,980 (GRCm39) |
H4799N |
possibly damaging |
Het |
Or1f12 |
T |
C |
13: 21,722,122 (GRCm39) |
K3E |
probably benign |
Het |
Or4p4 |
A |
G |
2: 88,482,729 (GRCm39) |
K78E |
probably damaging |
Het |
Or52e18 |
T |
C |
7: 104,609,356 (GRCm39) |
I194M |
probably damaging |
Het |
Or7g22 |
A |
G |
9: 19,048,353 (GRCm39) |
I21M |
probably benign |
Het |
Pcdhgb5 |
T |
C |
18: 37,866,302 (GRCm39) |
F699S |
probably damaging |
Het |
Phtf2 |
T |
C |
5: 21,007,038 (GRCm39) |
E175G |
probably benign |
Het |
Pira1 |
G |
A |
7: 3,740,075 (GRCm39) |
T340I |
probably damaging |
Het |
Ppp2r5c |
A |
G |
12: 110,517,519 (GRCm39) |
H218R |
possibly damaging |
Het |
Ptgs2 |
A |
G |
1: 149,979,785 (GRCm39) |
R297G |
probably damaging |
Het |
Rapgef3 |
A |
T |
15: 97,648,747 (GRCm39) |
D619E |
probably benign |
Het |
Ric1 |
G |
A |
19: 29,552,191 (GRCm39) |
V321I |
probably benign |
Het |
Ripor1 |
T |
C |
8: 106,344,105 (GRCm39) |
V413A |
probably damaging |
Het |
Rsf1 |
G |
T |
7: 97,288,464 (GRCm39) |
|
probably null |
Het |
Sccpdh |
A |
G |
1: 179,504,017 (GRCm39) |
D122G |
probably damaging |
Het |
Slco1a5 |
G |
T |
6: 142,208,418 (GRCm39) |
N124K |
probably damaging |
Het |
Snrnp200 |
A |
G |
2: 127,071,051 (GRCm39) |
T1111A |
probably benign |
Het |
Stard9 |
G |
A |
2: 120,534,911 (GRCm39) |
G3723S |
probably benign |
Het |
Tanc2 |
T |
A |
11: 105,725,988 (GRCm39) |
V384E |
probably damaging |
Het |
Tbrg1 |
A |
G |
9: 37,568,296 (GRCm39) |
F49L |
possibly damaging |
Het |
Tecta |
A |
G |
9: 42,288,927 (GRCm39) |
F546S |
probably damaging |
Het |
Tmem132c |
A |
G |
5: 127,437,176 (GRCm39) |
R222G |
probably benign |
Het |
Trub2 |
C |
T |
2: 29,668,739 (GRCm39) |
|
probably null |
Het |
Tti1 |
G |
T |
2: 157,849,418 (GRCm39) |
P607Q |
probably damaging |
Het |
Vmn1r62 |
T |
A |
7: 5,678,726 (GRCm39) |
F136I |
possibly damaging |
Het |
Vmn2r111 |
T |
A |
17: 22,790,469 (GRCm39) |
H179L |
probably benign |
Het |
Wdfy4 |
A |
T |
14: 32,699,063 (GRCm39) |
C2703* |
probably null |
Het |
Wdfy4 |
G |
A |
14: 32,826,072 (GRCm39) |
P1193L |
|
Het |
Wipf3 |
A |
G |
6: 54,460,816 (GRCm39) |
K88R |
probably benign |
Het |
Zfp641 |
C |
T |
15: 98,186,856 (GRCm39) |
G256R |
probably damaging |
Het |
Zfp993 |
T |
A |
4: 146,741,972 (GRCm39) |
C99S |
probably benign |
Het |
|
Other mutations in Sec16a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00337:Sec16a
|
APN |
2 |
26,329,499 (GRCm39) |
missense |
probably benign |
0.15 |
IGL00435:Sec16a
|
APN |
2 |
26,320,113 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00469:Sec16a
|
APN |
2 |
26,318,312 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01622:Sec16a
|
APN |
2 |
26,328,915 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01623:Sec16a
|
APN |
2 |
26,328,915 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02158:Sec16a
|
APN |
2 |
26,306,644 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02188:Sec16a
|
APN |
2 |
26,326,020 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02445:Sec16a
|
APN |
2 |
26,312,052 (GRCm39) |
missense |
probably benign |
|
IGL02568:Sec16a
|
APN |
2 |
26,326,054 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02710:Sec16a
|
APN |
2 |
26,320,142 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02735:Sec16a
|
APN |
2 |
26,318,149 (GRCm39) |
splice site |
probably benign |
|
IGL02964:Sec16a
|
APN |
2 |
26,309,735 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03027:Sec16a
|
APN |
2 |
26,313,601 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03073:Sec16a
|
APN |
2 |
26,329,195 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03297:Sec16a
|
APN |
2 |
26,329,202 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03339:Sec16a
|
APN |
2 |
26,325,945 (GRCm39) |
missense |
probably benign |
|
H8562:Sec16a
|
UTSW |
2 |
26,331,517 (GRCm39) |
missense |
probably benign |
|
IGL03050:Sec16a
|
UTSW |
2 |
26,305,759 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4486001:Sec16a
|
UTSW |
2 |
26,315,785 (GRCm39) |
missense |
|
|
R0039:Sec16a
|
UTSW |
2 |
26,313,926 (GRCm39) |
missense |
probably benign |
0.03 |
R0095:Sec16a
|
UTSW |
2 |
26,315,772 (GRCm39) |
splice site |
probably null |
|
R0095:Sec16a
|
UTSW |
2 |
26,315,772 (GRCm39) |
splice site |
probably null |
|
R0189:Sec16a
|
UTSW |
2 |
26,314,426 (GRCm39) |
splice site |
probably null |
|
R0255:Sec16a
|
UTSW |
2 |
26,321,198 (GRCm39) |
missense |
probably damaging |
0.97 |
R0278:Sec16a
|
UTSW |
2 |
26,318,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R0739:Sec16a
|
UTSW |
2 |
26,331,063 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0743:Sec16a
|
UTSW |
2 |
26,309,734 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1446:Sec16a
|
UTSW |
2 |
26,313,579 (GRCm39) |
missense |
probably benign |
0.00 |
R1466:Sec16a
|
UTSW |
2 |
26,321,169 (GRCm39) |
missense |
probably damaging |
0.98 |
R1466:Sec16a
|
UTSW |
2 |
26,321,169 (GRCm39) |
missense |
probably damaging |
0.98 |
R1501:Sec16a
|
UTSW |
2 |
26,330,057 (GRCm39) |
missense |
probably benign |
0.16 |
R1524:Sec16a
|
UTSW |
2 |
26,318,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R1584:Sec16a
|
UTSW |
2 |
26,321,169 (GRCm39) |
missense |
probably damaging |
0.98 |
R1649:Sec16a
|
UTSW |
2 |
26,315,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R1744:Sec16a
|
UTSW |
2 |
26,329,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R1959:Sec16a
|
UTSW |
2 |
26,320,144 (GRCm39) |
missense |
probably benign |
0.00 |
R1973:Sec16a
|
UTSW |
2 |
26,316,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2005:Sec16a
|
UTSW |
2 |
26,329,092 (GRCm39) |
missense |
probably benign |
0.27 |
R2073:Sec16a
|
UTSW |
2 |
26,330,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2074:Sec16a
|
UTSW |
2 |
26,330,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Sec16a
|
UTSW |
2 |
26,330,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Sec16a
|
UTSW |
2 |
26,303,757 (GRCm39) |
intron |
probably benign |
|
R2472:Sec16a
|
UTSW |
2 |
26,329,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R2512:Sec16a
|
UTSW |
2 |
26,329,037 (GRCm39) |
missense |
probably benign |
0.00 |
R2520:Sec16a
|
UTSW |
2 |
26,331,368 (GRCm39) |
nonsense |
probably null |
|
R2571:Sec16a
|
UTSW |
2 |
26,329,343 (GRCm39) |
missense |
probably benign |
0.08 |
R3105:Sec16a
|
UTSW |
2 |
26,328,433 (GRCm39) |
missense |
probably benign |
0.14 |
R3508:Sec16a
|
UTSW |
2 |
26,315,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R3809:Sec16a
|
UTSW |
2 |
26,331,825 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3912:Sec16a
|
UTSW |
2 |
26,304,399 (GRCm39) |
missense |
probably damaging |
0.97 |
R4292:Sec16a
|
UTSW |
2 |
26,312,167 (GRCm39) |
missense |
probably benign |
0.01 |
R4293:Sec16a
|
UTSW |
2 |
26,312,167 (GRCm39) |
missense |
probably benign |
0.01 |
R4294:Sec16a
|
UTSW |
2 |
26,312,167 (GRCm39) |
missense |
probably benign |
0.01 |
R4576:Sec16a
|
UTSW |
2 |
26,321,131 (GRCm39) |
nonsense |
probably null |
|
R4611:Sec16a
|
UTSW |
2 |
26,331,817 (GRCm39) |
missense |
probably benign |
0.04 |
R4627:Sec16a
|
UTSW |
2 |
26,321,080 (GRCm39) |
splice site |
probably null |
|
R4627:Sec16a
|
UTSW |
2 |
26,319,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4662:Sec16a
|
UTSW |
2 |
26,320,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R4665:Sec16a
|
UTSW |
2 |
26,302,970 (GRCm39) |
intron |
probably benign |
|
R4906:Sec16a
|
UTSW |
2 |
26,331,979 (GRCm39) |
unclassified |
probably benign |
|
R4967:Sec16a
|
UTSW |
2 |
26,302,883 (GRCm39) |
missense |
probably benign |
0.00 |
R4983:Sec16a
|
UTSW |
2 |
26,329,531 (GRCm39) |
missense |
probably benign |
|
R5033:Sec16a
|
UTSW |
2 |
26,309,661 (GRCm39) |
missense |
probably benign |
0.00 |
R5251:Sec16a
|
UTSW |
2 |
26,329,357 (GRCm39) |
missense |
probably benign |
0.00 |
R5391:Sec16a
|
UTSW |
2 |
26,330,044 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5457:Sec16a
|
UTSW |
2 |
26,330,280 (GRCm39) |
missense |
probably benign |
0.01 |
R5530:Sec16a
|
UTSW |
2 |
26,329,264 (GRCm39) |
missense |
probably benign |
0.00 |
R5645:Sec16a
|
UTSW |
2 |
26,329,907 (GRCm39) |
missense |
probably benign |
0.01 |
R5661:Sec16a
|
UTSW |
2 |
26,329,649 (GRCm39) |
missense |
probably benign |
0.01 |
R5770:Sec16a
|
UTSW |
2 |
26,304,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R5830:Sec16a
|
UTSW |
2 |
26,330,853 (GRCm39) |
missense |
probably benign |
0.15 |
R5866:Sec16a
|
UTSW |
2 |
26,309,650 (GRCm39) |
missense |
probably benign |
0.00 |
R5875:Sec16a
|
UTSW |
2 |
26,323,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R5906:Sec16a
|
UTSW |
2 |
26,328,843 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5922:Sec16a
|
UTSW |
2 |
26,305,651 (GRCm39) |
missense |
probably benign |
0.05 |
R6076:Sec16a
|
UTSW |
2 |
26,313,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R6091:Sec16a
|
UTSW |
2 |
26,316,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R6295:Sec16a
|
UTSW |
2 |
26,318,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Sec16a
|
UTSW |
2 |
26,315,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R6309:Sec16a
|
UTSW |
2 |
26,328,583 (GRCm39) |
missense |
probably benign |
0.00 |
R6459:Sec16a
|
UTSW |
2 |
26,313,512 (GRCm39) |
missense |
probably benign |
0.04 |
R6520:Sec16a
|
UTSW |
2 |
26,316,118 (GRCm39) |
missense |
probably damaging |
1.00 |
R6631:Sec16a
|
UTSW |
2 |
26,329,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R6657:Sec16a
|
UTSW |
2 |
26,315,876 (GRCm39) |
nonsense |
probably null |
|
R6750:Sec16a
|
UTSW |
2 |
26,330,030 (GRCm39) |
missense |
probably benign |
0.00 |
R6852:Sec16a
|
UTSW |
2 |
26,331,431 (GRCm39) |
missense |
probably damaging |
0.99 |
R6860:Sec16a
|
UTSW |
2 |
26,320,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R6967:Sec16a
|
UTSW |
2 |
26,320,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6968:Sec16a
|
UTSW |
2 |
26,320,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6970:Sec16a
|
UTSW |
2 |
26,320,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6991:Sec16a
|
UTSW |
2 |
26,320,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R6993:Sec16a
|
UTSW |
2 |
26,313,586 (GRCm39) |
missense |
probably damaging |
0.99 |
R7009:Sec16a
|
UTSW |
2 |
26,326,014 (GRCm39) |
nonsense |
probably null |
|
R7057:Sec16a
|
UTSW |
2 |
26,315,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R7186:Sec16a
|
UTSW |
2 |
26,330,715 (GRCm39) |
nonsense |
probably null |
|
R7227:Sec16a
|
UTSW |
2 |
26,328,935 (GRCm39) |
missense |
probably benign |
0.01 |
R7234:Sec16a
|
UTSW |
2 |
26,329,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R7259:Sec16a
|
UTSW |
2 |
26,331,604 (GRCm39) |
missense |
probably benign |
0.00 |
R7326:Sec16a
|
UTSW |
2 |
26,329,729 (GRCm39) |
missense |
unknown |
|
R7371:Sec16a
|
UTSW |
2 |
26,331,734 (GRCm39) |
missense |
probably benign |
|
R7388:Sec16a
|
UTSW |
2 |
26,318,376 (GRCm39) |
missense |
|
|
R7414:Sec16a
|
UTSW |
2 |
26,313,643 (GRCm39) |
missense |
|
|
R7417:Sec16a
|
UTSW |
2 |
26,311,409 (GRCm39) |
missense |
|
|
R7501:Sec16a
|
UTSW |
2 |
26,331,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R7558:Sec16a
|
UTSW |
2 |
26,329,746 (GRCm39) |
missense |
|
|
R7696:Sec16a
|
UTSW |
2 |
26,305,645 (GRCm39) |
critical splice donor site |
probably null |
|
R7981:Sec16a
|
UTSW |
2 |
26,311,384 (GRCm39) |
critical splice donor site |
probably null |
|
R8131:Sec16a
|
UTSW |
2 |
26,300,958 (GRCm39) |
missense |
|
|
R8163:Sec16a
|
UTSW |
2 |
26,306,433 (GRCm39) |
missense |
|
|
R8825:Sec16a
|
UTSW |
2 |
26,313,586 (GRCm39) |
missense |
|
|
R8855:Sec16a
|
UTSW |
2 |
26,329,852 (GRCm39) |
missense |
probably benign |
0.16 |
R9165:Sec16a
|
UTSW |
2 |
26,313,645 (GRCm39) |
missense |
|
|
R9216:Sec16a
|
UTSW |
2 |
26,304,401 (GRCm39) |
missense |
|
|
R9283:Sec16a
|
UTSW |
2 |
26,313,904 (GRCm39) |
missense |
|
|
R9506:Sec16a
|
UTSW |
2 |
26,319,384 (GRCm39) |
critical splice donor site |
probably null |
|
R9581:Sec16a
|
UTSW |
2 |
26,328,647 (GRCm39) |
missense |
|
|
R9772:Sec16a
|
UTSW |
2 |
26,329,417 (GRCm39) |
missense |
possibly damaging |
0.87 |
X0011:Sec16a
|
UTSW |
2 |
26,305,655 (GRCm39) |
missense |
probably damaging |
1.00 |
X0034:Sec16a
|
UTSW |
2 |
26,306,709 (GRCm39) |
missense |
probably benign |
0.07 |
X0062:Sec16a
|
UTSW |
2 |
26,306,709 (GRCm39) |
missense |
probably benign |
0.07 |
Z1088:Sec16a
|
UTSW |
2 |
26,329,105 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Sec16a
|
UTSW |
2 |
26,328,760 (GRCm39) |
missense |
|
|
Z1177:Sec16a
|
UTSW |
2 |
26,329,333 (GRCm39) |
missense |
probably damaging |
0.99 |
|