NM_004431.5(EPHA2):c.2162G>A (p.Arg721Gln)
|
rs116506614
|
0.00073
|
NM_004431.5(EPHA2):c.1984G>A (p.Gly662Ser)
|
rs144342633
|
0.00025
|
NM_004431.5(EPHA2):c.1046C>T (p.Thr349Met)
|
rs200490325
|
0.00011
|
NM_004431.5(EPHA2):c.2826C>T (p.Asp942=)
|
rs143828420
|
0.00011
|
NM_004431.5(EPHA2):c.1283G>A (p.Arg428His)
|
rs138475231
|
0.00008
|
NM_004431.5(EPHA2):c.1720G>A (p.Val574Ile)
|
rs201325716
|
0.00006
|
NM_004431.5(EPHA2):c.442G>A (p.Asp148Asn)
|
rs754447639
|
0.00004
|
NM_004431.5(EPHA2):c.1118C>T (p.Ser373Phe)
|
rs758978165
|
0.00003
|
NM_004431.5(EPHA2):c.1697G>A (p.Arg566His)
|
rs750878968
|
0.00003
|
NM_004431.5(EPHA2):c.1843C>T (p.Arg615Trp)
|
rs373953344
|
0.00003
|
NM_004431.5(EPHA2):c.844A>G (p.Lys282Glu)
|
rs747087417
|
0.00002
|
NM_004431.5(EPHA2):c.1040G>A (p.Arg347His)
|
rs761928478
|
0.00001
|
NM_004431.5(EPHA2):c.2029C>T (p.Arg677Cys)
|
rs765261745
|
0.00001
|
NM_004431.5(EPHA2):c.2174C>G (p.Ala725Gly)
|
rs2024583180
|
0.00001
|
NM_004431.5(EPHA2):c.524G>A (p.Arg175His)
|
rs759687964
|
0.00001
|
NM_004431.5(EPHA2):c.890C>T (p.Thr297Met)
|
rs754323552
|
0.00001
|
NC_000001.10:g.(?_16460943)_(16482447_?)dup
|
|
|
NM_004431.5(EPHA2):c.1063G>A (p.Gly355Arg)
|
|
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NM_004431.5(EPHA2):c.1067G>A (p.Gly356Asp)
|
rs1248366791
|
|
NM_004431.5(EPHA2):c.1129G>A (p.Gly377Arg)
|
|
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NM_004431.5(EPHA2):c.1180C>T (p.Arg394Cys)
|
|
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NM_004431.5(EPHA2):c.1453C>A (p.Arg485Ser)
|
|
|
NM_004431.5(EPHA2):c.1456C>T (p.Arg486Cys)
|
|
|
NM_004431.5(EPHA2):c.1577C>T (p.Thr526Met)
|
|
|
NM_004431.5(EPHA2):c.1618G>A (p.Gly540Ser)
|
|
|
NM_004431.5(EPHA2):c.1743A>G (p.Gln581=)
|
|
|
NM_004431.5(EPHA2):c.1801G>T (p.Val601Leu)
|
|
|
NM_004431.5(EPHA2):c.1970G>C (p.Arg657Pro)
|
|
|
NM_004431.5(EPHA2):c.2329G>A (p.Gly777Ser)
|
rs922655349
|
|
NM_004431.5(EPHA2):c.2374C>T (p.Arg792Trp)
|
rs55869078
|
|
NM_004431.5(EPHA2):c.2736G>T (p.Trp912Cys)
|
rs903033191
|
|
NM_004431.5(EPHA2):c.2743T>C (p.Ser915Pro)
|
rs775490586
|
|
NM_004431.5(EPHA2):c.2826-35_2890del
|
|
|
NM_004431.5(EPHA2):c.2827G>A (p.Asp943Asn)
|
|
|
NM_004431.5(EPHA2):c.410G>A (p.Arg137His)
|
|
|
NM_004431.5(EPHA2):c.697C>T (p.His233Tyr)
|
|
|
NM_004431.5(EPHA2):c.924G>C (p.Glu308Asp)
|
rs759269511
|
|