ClinVar Miner

List of variants in gene TRAPPC12 reported as benign for not provided

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Gene type:
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Total variants: 32
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HGVS dbSNP gnomAD frequency
NM_016030.6(TRAPPC12):c.681T>C (p.Phe227=) rs10865541 0.62092
NM_016030.6(TRAPPC12):c.2181C>T (p.Phe727=) rs6767 0.44208
NM_016030.6(TRAPPC12):c.1773G>C (p.Leu591=) rs4971514 0.41612
NM_016030.6(TRAPPC12):c.901A>G (p.Ser301Gly) rs11686212 0.39295
NM_016030.6(TRAPPC12):c.432C>T (p.Ala144=) rs11127423 0.22847
NM_016030.6(TRAPPC12):c.2157C>T (p.Val719=) rs13986 0.14687
NM_016030.6(TRAPPC12):c.1965+18C>T rs13003061 0.11280
NM_016030.6(TRAPPC12):c.1842T>C (p.Asp614=) rs11548215 0.11196
NM_016030.6(TRAPPC12):c.1417+16T>C rs112370205 0.02827
NM_016030.6(TRAPPC12):c.1722T>C (p.Tyr574=) rs35407737 0.02054
NM_016030.6(TRAPPC12):c.1242C>T (p.Ser414=) rs1132171 0.01947
NM_016030.6(TRAPPC12):c.1777-15A>C rs73910562 0.01406
NM_016030.6(TRAPPC12):c.519C>T (p.Asp173=) rs184956144 0.01015
NM_016030.6(TRAPPC12):c.1164+3A>G rs115767701 0.00992
NM_016030.6(TRAPPC12):c.733C>T (p.Pro245Ser) rs200381361 0.00974
NM_016030.6(TRAPPC12):c.1603+12G>A rs76610791 0.00868
NM_016030.6(TRAPPC12):c.627C>T (p.Phe209=) rs140551015 0.00800
NM_016030.6(TRAPPC12):c.1244G>A (p.Gly415Glu) rs35775829 0.00721
NM_016030.6(TRAPPC12):c.1347A>G (p.Glu449=) rs117838642 0.00385
NM_016030.6(TRAPPC12):c.64G>A (p.Ala22Thr) rs200941005 0.00215
NM_016030.6(TRAPPC12):c.1445T>C (p.Ile482Thr) rs150167013 0.00184
NM_016030.6(TRAPPC12):c.145G>A (p.Glu49Lys) rs117747228 0.00063
NM_016030.6(TRAPPC12):c.175G>A (p.Ala59Thr) rs191638734 0.00002
NM_016030.6(TRAPPC12):c.1383C>T (p.Tyr461=)
NM_016030.6(TRAPPC12):c.1437G>A (p.Ser479=)
NM_016030.6(TRAPPC12):c.1603+15C>G
NM_016030.6(TRAPPC12):c.1677+12G>A
NM_016030.6(TRAPPC12):c.1755C>T (p.Gly585=)
NM_016030.6(TRAPPC12):c.1878-19A>T rs73910563
NM_016030.6(TRAPPC12):c.361G>A (p.Glu121Lys)
NM_016030.6(TRAPPC12):c.936C>T (p.Pro312=) rs371685284
NM_016030.6(TRAPPC12):c.993G>A (p.Val331=)

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