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Gene Protein AA change dbSNP Phenotype Chain Detail
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1 MYH14 Q7Z406 p.Pro31Thr rs590722 variant of unknown significance
3dtp
B
Detail
0.49 (T)
0.106 (N)
N
2 MYH14 Q7Z406 p.Arg88Gln rs185910660 variant of unknown significance
3dtp
B
Detail
(-)
(-)
N
3 MYH14 Q7Z406 p.Ser120Leu rs119103281 Deafness autosomal dominant type 4 (DFNA4) [MIM:600652]
3dtp
B
Detail
0.00 (D)
0.978 (D)
D ( Predicted by rules : 1 2 )
4 MYH14 Q7Z406 p.Met161Ile rs34773557 variant of unknown significance
3dtp
B
Detail
0.40 (T)
0.763 (D)
N
5 MYH14 Q7Z406 p.Ala176Thr rs138001307 variant of unknown significance
3dtp
B
Detail
0.07 (T)
0.995 (D)
D ( Predicted by rules : 1 2 )
4 MYH14 Q7Z406 p.Ile266Val - variant of unknown significance
3dtp
B
Detail
0.41 (T)
0.706 (D)
N
5 MYH14 Q7Z406 p.Ile268Val rs55645295 variant of unknown significance
3dtp
B
Detail
0.01 (D)
0.706 (D)
N
6 MYH14 Q7Z406 p.Pro334Ala rs34498817 variant of unknown significance
3dtp
B
Detail
0.58 (T)
0.634 (D)
N
7 MYH14 Q7Z406 p.Ser337Cys rs35315400 variant of unknown significance
3dtp
B
Detail
0.10 (T)
0.899 (D)
D ( Predicted by rules : 1 2 3 )
5 MYH14 Q7Z406 p.Thr348Met rs151082668 variant of unknown significance
3dtp
B
Detail
0.01 (D)
1 (D)
D ( Predicted by rules : 1 2 3 )
5 MYH14 Q7Z406 p.Arg353Gln rs139215122 variant of unknown significance
3dtp
B
Detail
0.25 (T)
0.074 (N)
D ( Predicted by rules : 1 )
3 MYH14 Q7Z406 p.Ser370Leu rs150806988 variant of unknown significance
3dtp
B
Detail
0.06 (T)
0.989 (D)
D ( Predicted by rules : 1 )
3 MYH14 Q7Z406 p.Gly376Cys rs119103280 Deafness autosomal dominant type 4 (DFNA4) [MIM:600652]
3dtp
B
Detail
0.00 (D)
1 (D)
D ( Predicted by rules : 1 )
3 MYH14 Q7Z406 p.Arg726Ser rs28940307 Deafness autosomal dominant type 4 (DFNA4) [MIM:600652]
3dtp
B
Detail
0.03 (D)
1 (D)
D ( Predicted by rules : 1 2 )
4 MYH14 Q7Z406 p.Asp805His rs181315427 variant of unknown significance
3dtp
B
Detail
(-)
(-)
N
5 MYH14 Q7Z406 p.Thr926Lys rs142134135 variant of unknown significance
3dtp
B
Detail
0.99 (T)
0.707 (D)
N
6 MYH14 Q7Z406 p.Arg933Leu rs113993956 variant of unknown significance
3dtp
B
Detail
0.36 (T)
0.968 (D)
N
7 MYH14 Q7Z406 p.Leu976Phe rs28940306 Deafness autosomal dominant type 4 (DFNA4) [MIM:600652]
3dtp
B
Detail
0.74 (T)
0.998 (D)
N
8 MYH14 Q7Z406 p.Gln984Arg rs190283424 variant of unknown significance
3dtp
B
Detail
(-)
(-)
N
9 MYH14 Q7Z406 p.Gln1092His rs11672655 variant of unknown significance
Detail
0.09 (T)
0.356 (N)
N
10 MYH14 Q7Z406 p.Ala1154Val - variant of unknown significance
Detail
(-)
(-)
N
11 MYH14 Q7Z406 p.Ala1209Glu rs11669191 variant of unknown significance
Detail
0.97 (T)
0.211 (N)
N
12 MYH14 Q7Z406 p.Ala1304Thr rs148054042 variant of unknown significance
Detail
0.59 (T)
0.009 (N)
N
13 MYH14 Q7Z406 p.Arg1378Trp rs115019972 variant of unknown significance
Detail
0.01 (D)
0.998 (D)
N
14 MYH14 Q7Z406 p.Arg1381His rs188682445 variant of unknown significance
Detail
(-)
(-)
N
15 MYH14 Q7Z406 p.Val1432Met rs112716976 variant of unknown significance
Detail
0.27 (T)
0.019 (N)
N
16 MYH14 Q7Z406 p.Arg1439His rs187782753 variant of unknown significance
Detail
(-)
(-)
N
17 MYH14 Q7Z406 p.Gln1455Glu rs141995460 variant of unknown significance
Detail
1.00 (T)
0.192 (N)
N
18 MYH14 Q7Z406 p.Arg1488His rs185232438 variant of unknown significance
Detail
(-)
(-)
N
19 MYH14 Q7Z406 p.Arg1521Gln rs140118363 variant of unknown significance
Detail
0.53 (T)
0.976 (D)
N
20 MYH14 Q7Z406 p.Arg1527Gln rs150029590 variant of unknown significance
Detail
0.60 (T)
0.794 (D)
N
21 MYH14 Q7Z406 p.Ala1528Ser rs145522874 variant of unknown significance
Detail
0.66 (T)
0.363 (N)
N
22 MYH14 Q7Z406 p.Val1540Ile rs680446 variant of unknown significance
Detail
0.46 (T)
0.075 (N)
N
23 MYH14 Q7Z406 p.Arg1549Gln rs76509044 variant of unknown significance
Detail
0.61 (T)
0.611 (D)
N
24 MYH14 Q7Z406 p.Asn1559Ser - variant of unknown significance
Detail
0.74 (T)
0 (N)
N
25 MYH14 Q7Z406 p.Glu1594Lys rs140157424 variant of unknown significance
Detail
0.94 (T)
0.986 (D)
N
26 MYH14 Q7Z406 p.Glu1605Gly rs77026959 variant of unknown significance
Detail
0.35 (T)
0.97 (D)
N
27 MYH14 Q7Z406 p.Arg1817His rs11882073 variant of unknown significance
Detail
0.51 (T)
0.984 (D)
N
28 MYH14 Q7Z406 p.Arg1826Cys rs187789045 variant of unknown significance
Detail
(-)
(-)
N