ClinVar Miner

List of variants in gene HSPA12A studied for not specified

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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_025015.3(HSPA12A):c.613G>A (p.Ala205Thr) rs371208406 0.00031
NM_025015.3(HSPA12A):c.1576G>A (p.Ala526Thr) rs200715815 0.00027
NM_025015.3(HSPA12A):c.1684C>T (p.Arg562Trp) rs187495430 0.00022
NM_025015.3(HSPA12A):c.1570G>T (p.Asp524Tyr) rs202107187 0.00009
NM_025015.3(HSPA12A):c.902T>C (p.Ile301Thr) rs199615590 0.00008
NM_025015.3(HSPA12A):c.1462C>T (p.Pro488Ser) rs1033829945 0.00005
NM_025015.3(HSPA12A):c.787G>A (p.Val263Ile) rs782064654 0.00005
NM_025015.3(HSPA12A):c.818G>C (p.Gly273Ala) rs782609994 0.00005
NM_025015.3(HSPA12A):c.938T>C (p.Val313Ala) rs782489411 0.00005
NM_025015.3(HSPA12A):c.1699G>A (p.Val567Ile) rs146839286 0.00004
NM_025015.3(HSPA12A):c.1979T>C (p.Ile660Thr) rs369963832 0.00004
NM_025015.3(HSPA12A):c.721G>A (p.Ala241Thr) rs375461005 0.00004
NM_025015.3(HSPA12A):c.961G>A (p.Val321Ile) rs781974587 0.00004
NM_025015.3(HSPA12A):c.1066G>A (p.Glu356Lys) rs781918083 0.00003
NM_025015.3(HSPA12A):c.1411G>A (p.Glu471Lys) rs782537687 0.00003
NM_025015.3(HSPA12A):c.569C>T (p.Ser190Leu) rs782137661 0.00003
NM_025015.3(HSPA12A):c.802G>A (p.Gly268Ser) rs781929997 0.00003
NM_025015.3(HSPA12A):c.1456G>A (p.Glu486Lys) rs782819530 0.00002
NM_025015.3(HSPA12A):c.1508G>A (p.Arg503Gln) rs782470572 0.00002
NM_025015.3(HSPA12A):c.1621G>A (p.Val541Met) rs781946508 0.00002
NM_025015.3(HSPA12A):c.1978A>G (p.Ile660Val) rs782412500 0.00002
NM_025015.3(HSPA12A):c.1757G>A (p.Arg586His) rs375255169 0.00001
NM_025015.3(HSPA12A):c.322G>A (p.Glu108Lys) rs781817907 0.00001
NM_025015.3(HSPA12A):c.527T>G (p.Phe176Cys) rs1377333802 0.00001
NM_025015.3(HSPA12A):c.697C>G (p.Leu233Val) rs1398154073 0.00001
NM_025015.3(HSPA12A):c.749G>A (p.Arg250Gln) rs1195155414 0.00001
NM_025015.3(HSPA12A):c.829A>T (p.Thr277Ser) rs1311274453 0.00001
NM_025015.3(HSPA12A):c.1021G>T (p.Ala341Ser)
NM_025015.3(HSPA12A):c.1063T>A (p.Phe355Ile)
NM_025015.3(HSPA12A):c.1088T>A (p.Phe363Tyr)
NM_025015.3(HSPA12A):c.1095G>T (p.Glu365Asp) rs1554878304
NM_025015.3(HSPA12A):c.1133C>G (p.Ala378Gly) rs1554878297
NM_025015.3(HSPA12A):c.1229T>C (p.Ile410Thr)
NM_025015.3(HSPA12A):c.1252G>A (p.Gly418Arg)
NM_025015.3(HSPA12A):c.130G>A (p.Asp44Asn)
NM_025015.3(HSPA12A):c.1396C>G (p.Leu466Val)
NM_025015.3(HSPA12A):c.145G>A (p.Val49Ile)
NM_025015.3(HSPA12A):c.1480G>A (p.Val494Met)
NM_025015.3(HSPA12A):c.1639G>A (p.Glu547Lys)
NM_025015.3(HSPA12A):c.1640A>G (p.Glu547Gly)
NM_025015.3(HSPA12A):c.1652C>T (p.Pro551Leu)
NM_025015.3(HSPA12A):c.169G>C (p.Val57Leu)
NM_025015.3(HSPA12A):c.1822G>A (p.Asp608Asn)
NM_025015.3(HSPA12A):c.1849G>A (p.Gly617Arg)
NM_025015.3(HSPA12A):c.1895G>A (p.Ser632Asn)
NM_025015.3(HSPA12A):c.1937T>G (p.Met646Arg)
NM_025015.3(HSPA12A):c.1945G>A (p.Gly649Arg) rs868970051
NM_025015.3(HSPA12A):c.2011G>A (p.Asp671Asn)
NM_025015.3(HSPA12A):c.2012A>C (p.Asp671Ala)
NM_025015.3(HSPA12A):c.231G>T (p.Glu77Asp) rs1554882213
NM_025015.3(HSPA12A):c.31G>T (p.Gly11Trp) rs1248793492
NM_025015.3(HSPA12A):c.326G>A (p.Arg109Lys)
NM_025015.3(HSPA12A):c.556G>A (p.Asp186Asn)
NM_025015.3(HSPA12A):c.568T>G (p.Ser190Ala) rs2493380218
NM_025015.3(HSPA12A):c.644T>C (p.Met215Thr)
NM_025015.3(HSPA12A):c.682G>A (p.Glu228Lys)
NM_025015.3(HSPA12A):c.740G>A (p.Arg247Gln)
NM_025015.3(HSPA12A):c.754C>T (p.His252Tyr)
NM_025015.3(HSPA12A):c.859C>T (p.Arg287Trp)
NM_025015.3(HSPA12A):c.952G>A (p.Gly318Ser)
NM_025015.3(HSPA12A):c.986G>A (p.Arg329Gln)

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