Browse variants

id CHR POS REF ALT HGVS c. HGVS p. GENE RSID Mean user class Consensus classification Review state
11084 chr9 69225336 G A
c.985G>A
p.Val329Ile
2.5
B
20086 chr9 69227879 A C
c.1319+6A>C
-
- 3.0
B
17615 chr9 69228039 A C
c.1378A>C
p.Lys460Gln
- 3.0
B
18312 chr9 69230128 C T
c.1567C>T
p.Leu523Phe
- 3.0
B
13848 chr9 69230146 A G
c.1585A>G
p.Asn529Asp
3.0
B
24181 chr9 69236087 G C
c.1840G>C
p.Glu614Gln
- 3.0
B
1892 chr9 69237907 G A
c.2209G>A
p.Gly737Ser
3.0
B
14709 chr9 69238694 G C
c.2276-16G>C
-
- 3.0
B
25187 chr9 69239955 G C
c.2374G>C
p.Asp792His
- 3.0
B
22124 chr9 69248006 C T
c.2668-6C>T
-
- 3.0
B
6906 chr9 69248024 G T
c.2680G>T
p.Asp894Tyr
- 3.0
B
10002 chr9 69248038 A C
c.2694A>C
p.Glu898Asp
- 3.0
B
12500 chr9 69248110 T A
c.2766T>A
p.Phe922Leu
- 3.0
B
28239 chr9 69249418 G A
c.2924G>A
p.Arg975Lys
- 3.0
B
27259 chr9 69251105 C T
c.3062C>T
p.Ala1021Val
- 3.0
B
29314 chr9 69251197 C G
c.3154C>G
p.Pro1052Ala
- 3.0
B
8975 chr9 69251207 C T
c.3164C>T
p.Pro1055Leu
- 3.0
B
4507 chr9 70282467 C T
c.865C>T
p.Arg289Cys
3.0
B
5187 chr9 72052304 T C
c.412A>G
p.Asn138Asp
- 3.0
B
8444 chr9 76233501 G A
c.2771G>A
p.Trp924Ter
- 3.0
B