NM_000702.4(ATP1A2):c.381+16C>T
|
rs2820581
|
0.95274
|
NM_000702.4(ATP1A2):c.1119G>A (p.Ser373=)
|
rs1063125
|
0.18359
|
NM_000702.4(ATP1A2):c.3034+14C>T
|
rs41288127
|
0.13198
|
NM_000702.4(ATP1A2):c.2259C>T (p.Ala753=)
|
rs17846715
|
0.09246
|
NM_000702.4(ATP1A2):c.1704C>T (p.Phe568=)
|
rs17846714
|
0.03612
|
NM_000702.4(ATP1A2):c.1652-11C>G
|
rs17846713
|
0.03344
|
NM_000702.4(ATP1A2):c.1125G>A (p.Lys375=)
|
rs61734526
|
0.00323
|
NM_000702.4(ATP1A2):c.836G>A (p.Arg279Gln)
|
rs373178892
|
0.00056
|
NM_000702.4(ATP1A2):c.1474G>A (p.Glu492Lys)
|
rs142348542
|
0.00055
|
NM_000702.4(ATP1A2):c.1470C>T (p.Ile490=)
|
rs111405592
|
0.00048
|
NM_000702.4(ATP1A2):c.339C>T (p.Tyr113=)
|
rs148929192
|
0.00023
|
NM_000702.4(ATP1A2):c.2229C>T (p.Ala743=)
|
rs138381089
|
0.00017
|
NM_000702.4(ATP1A2):c.1251G>C (p.Thr417=)
|
rs142309356
|
0.00010
|
NM_000702.4(ATP1A2):c.1581C>G (p.Leu527=)
|
rs371520433
|
0.00010
|
NM_000702.4(ATP1A2):c.1332C>T (p.Asp444=)
|
rs765455081
|
0.00007
|
NM_000702.4(ATP1A2):c.1761T>C (p.Ser587=)
|
rs199621678
|
0.00006
|
NM_000702.4(ATP1A2):c.1735A>G (p.Lys579Glu)
|
rs535175099
|
0.00005
|
NM_000702.4(ATP1A2):c.987C>T (p.Asn329=)
|
rs770381135
|
0.00005
|
NM_000702.4(ATP1A2):c.789G>A (p.Thr263=)
|
rs748890267
|
0.00002
|
NM_000702.4(ATP1A2):c.1244C>T (p.Thr415Met)
|
rs121918618
|
0.00001
|
NM_000702.4(ATP1A2):c.2636G>A (p.Arg879Gln)
|
rs761597771
|
0.00001
|
NM_000702.4(ATP1A2):c.888C>T (p.Val296=)
|
rs767314566
|
0.00001
|
NM_000702.4(ATP1A2):c.1112T>A (p.Ile371Asn)
|
|
|
NM_000702.4(ATP1A2):c.1216+1G>A
|
|
|
NM_000702.4(ATP1A2):c.13-11_13-8del
|
rs373796693
|
|
NM_000702.4(ATP1A2):c.1417C>T (p.Pro473Ser)
|
|
|
NM_000702.4(ATP1A2):c.1816G>A (p.Ala606Thr)
|
rs1414742926
|
|
NM_000702.4(ATP1A2):c.2285-1G>A
|
|
|
NM_000702.4(ATP1A2):c.2287C>T (p.Arg763Cys)
|
rs2101995435
|
|
NM_000702.4(ATP1A2):c.2439+3G>C
|
|
|
NM_000702.4(ATP1A2):c.2454_2456del (p.Leu819del)
|
|
|
NM_000702.4(ATP1A2):c.246C>G (p.Pro82=)
|
rs537472446
|
|
NM_000702.4(ATP1A2):c.2496G>A (p.Gln832=)
|
|
|
NM_000702.4(ATP1A2):c.2553C>T (p.Tyr851=)
|
|
|
NM_000702.4(ATP1A2):c.262del (p.Val88fs)
|
|
|
NM_000702.4(ATP1A2):c.2787T>C (p.Ala929=)
|
|
|
NM_000702.4(ATP1A2):c.2841-20dup
|
rs397775888
|
|
NM_000702.4(ATP1A2):c.456C>T (p.Ser152=)
|
|
|
NM_000702.4(ATP1A2):c.749-4G>A
|
|
|
NM_000702.4(ATP1A2):c.889G>A (p.Ala297Thr)
|
rs181618883
|
|
NM_000702.4(ATP1A2):c.970G>T (p.Gly324Cys)
|
|
|