ClinVar Miner

List of variants in gene VIPAS39 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_001193315.2(VIPAS39):c.1455C>A (p.Ser485Arg) rs145453157 0.00129
NM_001193315.2(VIPAS39):c.598-25C>T rs112062894 0.00125
NM_001193315.2(VIPAS39):c.136G>A (p.Val46Met) rs148360332 0.00106
NM_001193315.2(VIPAS39):c.1460C>T (p.Ser487Leu) rs140365206 0.00084
NM_001193315.2(VIPAS39):c.504+9A>G rs371762531 0.00028
NM_001193315.2(VIPAS39):c.1254T>C (p.Asn418=) rs188105111 0.00008
NM_001193315.2(VIPAS39):c.78C>T (p.Asp26=) rs112217896 0.00007
NM_001193315.2(VIPAS39):c.632-9G>A rs370850533 0.00004
NM_001193315.2(VIPAS39):c.1005A>T (p.Thr335=) rs765454382 0.00002
NM_001193315.2(VIPAS39):c.1266+5T>C rs762123926 0.00001
NM_001193315.2(VIPAS39):c.1356+8C>T rs988006454 0.00001
NM_001193315.2(VIPAS39):c.837-43T>C rs886038667 0.00001
NM_001193315.2(VIPAS39):c.1008A>C (p.Thr336=)
NM_001193315.2(VIPAS39):c.1267-7C>T
NM_001193315.2(VIPAS39):c.1323C>G (p.Ala441=)
NM_001193315.2(VIPAS39):c.1335G>A (p.Lys445=)
NM_001193315.2(VIPAS39):c.1357-35G>C rs113067724
NM_001193315.2(VIPAS39):c.45C>G (p.Ser15=)
NM_001193315.2(VIPAS39):c.488G>A (p.Arg163His)
NM_001193315.2(VIPAS39):c.51C>T (p.Phe17=)
NM_001193315.2(VIPAS39):c.734+7A>G
NM_001193315.2(VIPAS39):c.828C>T (p.Thr276=)

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