NM_001371596.2(MFSD8):c.1006G>C (p.Glu336Gln)
|
rs150418024
|
0.00299
|
NM_001371596.2(MFSD8):c.590G>A (p.Gly197Asp)
|
rs28544073
|
0.00184
|
NM_001371596.2(MFSD8):c.886G>A (p.Asp296Asn)
|
rs147295085
|
0.00054
|
NM_001371596.2(MFSD8):c.656T>C (p.Phe219Ser)
|
rs112734134
|
0.00048
|
NM_001371596.2(MFSD8):c.1136T>C (p.Phe379Ser)
|
rs191172038
|
0.00030
|
NM_001371596.2(MFSD8):c.677T>C (p.Ile226Thr)
|
rs200591471
|
0.00019
|
NM_001371596.2(MFSD8):c.206C>T (p.Pro69Leu)
|
rs147750747
|
0.00013
|
NM_001371596.2(MFSD8):c.934A>G (p.Ile312Val)
|
rs77098161
|
0.00013
|
NM_001371596.2(MFSD8):c.1205C>T (p.Ser402Leu)
|
rs200745039
|
0.00010
|
NM_001371596.2(MFSD8):c.576C>G (p.Phe192Leu)
|
rs777020801
|
0.00010
|
NM_001371596.2(MFSD8):c.592G>A (p.Val198Met)
|
rs377029630
|
0.00010
|
NM_001371596.2(MFSD8):c.409G>A (p.Val137Ile)
|
rs146479250
|
0.00006
|
NM_001371596.2(MFSD8):c.772C>G (p.Gln258Glu)
|
rs976533060
|
0.00005
|
NM_001371596.2(MFSD8):c.1174G>A (p.Glu392Lys)
|
rs773610115
|
0.00004
|
NM_001371596.2(MFSD8):c.1475T>C (p.Ile492Thr)
|
rs183448311
|
0.00004
|
NM_001371596.2(MFSD8):c.14G>C (p.Arg5Pro)
|
rs139409959
|
0.00004
|
NM_001371596.2(MFSD8):c.34C>T (p.Pro12Ser)
|
rs371882083
|
0.00004
|
NM_001371596.2(MFSD8):c.291G>C (p.Trp97Cys)
|
rs796052749
|
0.00003
|
NM_001371596.2(MFSD8):c.343G>A (p.Val115Met)
|
rs183450731
|
0.00003
|
NM_001371596.2(MFSD8):c.652G>A (p.Ala218Thr)
|
rs368614789
|
0.00003
|
NM_001371596.2(MFSD8):c.1107G>C (p.Leu369Phe)
|
rs747197852
|
0.00002
|
NM_001371596.2(MFSD8):c.1535G>A (p.Arg512Lys)
|
rs796052748
|
0.00002
|
NM_001371596.2(MFSD8):c.-21C>T
|
rs200352565
|
0.00001
|
NM_001371596.2(MFSD8):c.1043G>C (p.Trp348Ser)
|
rs796052746
|
0.00001
|
NM_001371596.2(MFSD8):c.1262C>T (p.Thr421Ile)
|
rs765587961
|
0.00001
|
NM_001371596.2(MFSD8):c.15G>A (p.Arg5=)
|
rs762559863
|
0.00001
|
NM_001371596.2(MFSD8):c.350C>G (p.Ala117Gly)
|
rs759795397
|
0.00001
|
NM_001371596.2(MFSD8):c.706C>T (p.Arg236Cys)
|
rs758002981
|
0.00001
|
NM_001371596.2(MFSD8):c.832G>A (p.Val278Met)
|
rs796052743
|
0.00001
|
NM_001371596.2(MFSD8):c.838C>G (p.Leu280Val)
|
rs749001842
|
0.00001
|
NM_001371596.2(MFSD8):c.863+4A>G
|
rs752035164
|
0.00001
|
NM_001371596.2(MFSD8):c.863C>T (p.Thr288Ile)
|
rs755384900
|
0.00001
|
NM_001371596.2(MFSD8):c.975A>G (p.Leu325=)
|
rs570989221
|
0.00001
|
NM_001371596.2(MFSD8):c.1006G>A (p.Glu336Lys)
|
rs150418024
|
|
NM_001371596.2(MFSD8):c.1130C>A (p.Thr377Asn)
|
|
|
NM_001371596.2(MFSD8):c.115A>G (p.Ile39Val)
|
rs201739608
|
|
NM_001371596.2(MFSD8):c.115A>T (p.Ile39Phe)
|
rs201739608
|
|
NM_001371596.2(MFSD8):c.1180G>A (p.Asp394Asn)
|
rs768627011
|
|
NM_001371596.2(MFSD8):c.1403G>A (p.Gly468Glu)
|
rs1560715852
|
|
NM_001371596.2(MFSD8):c.1408A>G (p.Met470Val)
|
rs764549054
|
|
NM_001371596.2(MFSD8):c.1420C>G (p.Gln474Glu)
|
|
|
NM_001371596.2(MFSD8):c.1420C>T (p.Gln474Ter)
|
rs370663969
|
|
NM_001371596.2(MFSD8):c.150T>C (p.Ser50=)
|
|
|
NM_001371596.2(MFSD8):c.211G>A (p.Ala71Thr)
|
rs796052741
|
|
NM_001371596.2(MFSD8):c.230G>T (p.Gly77Val)
|
rs886043062
|
|
NM_001371596.2(MFSD8):c.290G>T (p.Trp97Leu)
|
|
|
NM_001371596.2(MFSD8):c.357C>T (p.Cys119=)
|
rs1553950874
|
|
NM_001371596.2(MFSD8):c.362A>G (p.Tyr121Cys)
|
rs118203978
|
|
NM_001371596.2(MFSD8):c.415C>T (p.Arg139Cys)
|
rs993001712
|
|
NM_001371596.2(MFSD8):c.427G>A (p.Gly143Arg)
|
rs1578911049
|
|
NM_001371596.2(MFSD8):c.439G>A (p.Gly147Arg)
|
rs2148921601
|
|
NM_001371596.2(MFSD8):c.529G>A (p.Ala177Thr)
|
rs1560751131
|
|
NM_001371596.2(MFSD8):c.534A>T (p.Leu178Phe)
|
|
|
NM_001371596.2(MFSD8):c.547G>T (p.Gly183Cys)
|
|
|
NM_001371596.2(MFSD8):c.590G>T (p.Gly197Val)
|
rs28544073
|
|
NM_001371596.2(MFSD8):c.59G>A (p.Ser20Asn)
|
|
|
NM_001371596.2(MFSD8):c.63-4del
|
rs755011754
|
|
NM_001371596.2(MFSD8):c.66A>G (p.Glu22=)
|
rs145529594
|
|
NM_001371596.2(MFSD8):c.697A>G (p.Arg233Gly)
|
|
|
NM_001371596.2(MFSD8):c.761C>T (p.Thr254Ile)
|
rs2148882488
|
|
NM_001371596.2(MFSD8):c.889A>C (p.Met297Leu)
|
rs1419909769
|
|
NM_001371596.2(MFSD8):c.890T>C (p.Met297Thr)
|
|
|
NM_001371596.2(MFSD8):c.895G>T (p.Ala299Ser)
|
rs796052750
|
|
NM_001371596.2(MFSD8):c.940G>T (p.Ala314Ser)
|
rs796052744
|
|
NM_001371596.2(MFSD8):c.998+4A>G
|
rs796052745
|
|
NM_152778.4(MFSD8):c.-75-2A>T
|
rs796052739
|
|
NM_152778.4(MFSD8):c.-75-2_-75-1inv
|
|
|