NM_006946.4(SPTBN2):c.157+5G>A
|
rs150159444
|
0.00081
|
NM_006946.4(SPTBN2):c.1456G>A (p.Ala486Thr)
|
rs143155918
|
0.00077
|
NM_006946.4(SPTBN2):c.7109G>A (p.Arg2370His)
|
rs145522851
|
0.00011
|
NM_006946.4(SPTBN2):c.1522A>C (p.Asn508His)
|
rs767775507
|
0.00005
|
NM_006946.4(SPTBN2):c.1160G>A (p.Arg387His)
|
rs772590586
|
0.00003
|
NM_006946.4(SPTBN2):c.6536G>A (p.Arg2179Gln)
|
rs759206588
|
0.00002
|
NM_006946.4(SPTBN2):c.6739T>C (p.Tyr2247His)
|
rs201138924
|
0.00002
|
NM_006946.4(SPTBN2):c.1973G>A (p.Arg658Gln)
|
rs753491527
|
0.00001
|
NM_006946.4(SPTBN2):c.2558C>T (p.Ala853Val)
|
rs773989387
|
0.00001
|
NM_006946.4(SPTBN2):c.2996G>A (p.Arg999His)
|
rs769417045
|
0.00001
|
NM_006946.4(SPTBN2):c.3867+3G>T
|
rs753473374
|
0.00001
|
NM_006946.4(SPTBN2):c.4986-5T>G
|
rs1371679359
|
0.00001
|
NM_006946.4(SPTBN2):c.6169G>T (p.Ala2057Ser)
|
rs1940323398
|
0.00001
|
NM_006946.4(SPTBN2):c.6374+15G>A
|
rs777633339
|
0.00001
|
NM_006946.4(SPTBN2):c.657-7C>G
|
rs758925003
|
0.00001
|
NM_006946.4(SPTBN2):c.6723-11G>A
|
rs758435668
|
0.00001
|
NM_006946.4(SPTBN2):c.6736G>A (p.Val2246Met)
|
rs369469000
|
0.00001
|
NM_006946.4(SPTBN2):c.6897-4A>G
|
rs1262014282
|
0.00001
|
NM_006946.4(SPTBN2):c.773-5T>C
|
rs1941832250
|
0.00001
|
NM_006946.4(SPTBN2):c.1081G>A (p.Glu361Lys)
|
|
|
NM_006946.4(SPTBN2):c.1438C>T (p.Arg480Trp)
|
rs397514749
|
|
NM_006946.4(SPTBN2):c.1472T>G (p.Leu491Arg)
|
|
|
NM_006946.4(SPTBN2):c.1549C>G (p.Arg517Gly)
|
rs371919862
|
|
NM_006946.4(SPTBN2):c.185C>T (p.Thr62Ile)
|
|
|
NM_006946.4(SPTBN2):c.1877T>C (p.Leu626Pro)
|
rs1554984881
|
|
NM_006946.4(SPTBN2):c.2012G>A (p.Arg671Gln)
|
rs1443491358
|
|
NM_006946.4(SPTBN2):c.2191C>T (p.Arg731Trp)
|
|
|
NM_006946.4(SPTBN2):c.3236C>T (p.Ala1079Val)
|
rs763021473
|
|
NM_006946.4(SPTBN2):c.3777-3C>G
|
|
|
NM_006946.4(SPTBN2):c.478T>C (p.Phe160Leu)
|
|
|
NM_006946.4(SPTBN2):c.5459AGC[5] (p.Gln1823dup)
|
rs1940534700
|
|
NM_006946.4(SPTBN2):c.5504C>T (p.Ala1835Val)
|
rs1940531426
|
|
NM_006946.4(SPTBN2):c.571G>T (p.Ala191Ser)
|
|
|
NM_006946.4(SPTBN2):c.6688G>C (p.Glu2230Gln)
|
rs1940196069
|
|
NM_006946.4(SPTBN2):c.7040G>A (p.Arg2347Gln)
|
|
|
NM_006946.4(SPTBN2):c.7044del (p.Gly2348_Met2349insTer)
|
|
|
NM_006946.4(SPTBN2):c.7096C>T (p.Pro2366Ser)
|
rs1940076802
|
|
NM_006946.4(SPTBN2):c.7103T>C (p.Val2368Ala)
|
rs1940076270
|
|
NM_006946.4(SPTBN2):c.901A>G (p.Met301Val)
|
rs897181468
|
|