ClinVar Miner

List of variants in gene ARHGAP31 reported as benign for Adams-Oliver syndrome 1

Included ClinVar conditions (2):
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Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_020754.4(ARHGAP31):c.*1712T>C rs72968497
NM_020754.4(ARHGAP31):c.*2355A>G rs12631504
NM_020754.4(ARHGAP31):c.*2693G>A rs12494943
NM_020754.4(ARHGAP31):c.*269A>G rs74767080
NM_020754.4(ARHGAP31):c.*2744A>G rs9289129
NM_020754.4(ARHGAP31):c.*2801C>T rs12495539
NM_020754.4(ARHGAP31):c.*3013G>A rs73857025
NM_020754.4(ARHGAP31):c.*590C>G rs145064712
NM_020754.4(ARHGAP31):c.*985_*986insC rs11391882
NM_020754.4(ARHGAP31):c.-194G>A rs4687994
NM_020754.4(ARHGAP31):c.-38C>A rs72960626
NM_020754.4(ARHGAP31):c.1065= (p.Val355=) rs4688001
NM_020754.4(ARHGAP31):c.1491C>A (p.Arg497=) rs61747387
NM_020754.4(ARHGAP31):c.1533A>G (p.Thr511=) rs77678258
NM_020754.4(ARHGAP31):c.1614A>G (p.Glu538=) rs61744411
NM_020754.4(ARHGAP31):c.1700C>T (p.Pro567Leu) rs61744178
NM_020754.4(ARHGAP31):c.1701G>A (p.Pro567=) rs2305249
NM_020754.4(ARHGAP31):c.1926+11T>C rs1463138
NM_020754.4(ARHGAP31):c.1926+5A>G rs1463139
NM_020754.4(ARHGAP31):c.2407G>A (p.Gly803Ser) rs3732413
NM_020754.4(ARHGAP31):c.2778G>A (p.Ala926=) rs61740281
NM_020754.4(ARHGAP31):c.3256G>A (p.Ala1086Thr) rs61744168
NM_020754.4(ARHGAP31):c.3615C>T (p.Pro1205=) rs3732414
NM_020754.4(ARHGAP31):c.540-6C>T rs16829782
NM_020754.4(ARHGAP31):c.881+7G>A rs78837524

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