ClinVar Miner

List of variants in gene LRRC56 reported by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_198075.4(LRRC56):c.1244G>A (p.Arg415Gln) rs138766042 0.00065
NM_198075.4(LRRC56):c.691G>A (p.Glu231Lys) rs373134692 0.00008
NM_198075.4(LRRC56):c.1573G>A (p.Ala525Thr) rs376628172 0.00006
NM_198075.4(LRRC56):c.1016G>A (p.Arg339Gln) rs558302518 0.00004
NM_198075.4(LRRC56):c.166C>T (p.Pro56Ser) rs372922076 0.00004
NM_198075.4(LRRC56):c.1232C>T (p.Pro411Leu) rs760126599 0.00002
NM_198075.4(LRRC56):c.403G>A (p.Ala135Thr) rs753522543 0.00001
NM_198075.4(LRRC56):c.1009G>A (p.Gly337Ser)
NM_198075.4(LRRC56):c.1022G>A (p.Arg341His)
NM_198075.4(LRRC56):c.104G>A (p.Ser35Asn)
NM_198075.4(LRRC56):c.1054G>A (p.Glu352Lys) rs773018391
NM_198075.4(LRRC56):c.1111C>G (p.Pro371Ala)
NM_198075.4(LRRC56):c.1153C>T (p.Leu385Phe)
NM_198075.4(LRRC56):c.1201C>T (p.Pro401Ser)
NM_198075.4(LRRC56):c.1208C>T (p.Ser403Phe)
NM_198075.4(LRRC56):c.1243C>T (p.Arg415Trp)
NM_198075.4(LRRC56):c.1300C>G (p.Pro434Ala)
NM_198075.4(LRRC56):c.1318C>T (p.Pro440Ser)
NM_198075.4(LRRC56):c.1367C>A (p.Pro456Gln)
NM_198075.4(LRRC56):c.1397C>T (p.Pro466Leu) rs772558927
NM_198075.4(LRRC56):c.1404G>C (p.Trp468Cys)
NM_198075.4(LRRC56):c.1532G>A (p.Arg511Gln) rs367633088
NM_198075.4(LRRC56):c.1550G>A (p.Gly517Asp)
NM_198075.4(LRRC56):c.1579A>G (p.Arg527Gly)
NM_198075.4(LRRC56):c.1612A>T (p.Ser538Cys)
NM_198075.4(LRRC56):c.1616C>G (p.Pro539Arg)
NM_198075.4(LRRC56):c.1621C>G (p.Pro541Ala)
NM_198075.4(LRRC56):c.166C>G (p.Pro56Ala)
NM_198075.4(LRRC56):c.172C>T (p.Arg58Trp)
NM_198075.4(LRRC56):c.202C>T (p.Leu68Phe)
NM_198075.4(LRRC56):c.316G>A (p.Gly106Ser)
NM_198075.4(LRRC56):c.325A>T (p.Arg109Trp)
NM_198075.4(LRRC56):c.34C>T (p.Arg12Trp)
NM_198075.4(LRRC56):c.374G>A (p.Arg125His)
NM_198075.4(LRRC56):c.431A>G (p.Tyr144Cys)
NM_198075.4(LRRC56):c.433G>A (p.Ala145Thr)
NM_198075.4(LRRC56):c.439T>A (p.Tyr147Asn)
NM_198075.4(LRRC56):c.439T>G (p.Tyr147Asp)
NM_198075.4(LRRC56):c.524T>G (p.Leu175Arg)
NM_198075.4(LRRC56):c.52G>A (p.Val18Ile) rs772525350
NM_198075.4(LRRC56):c.539A>C (p.Tyr180Ser)
NM_198075.4(LRRC56):c.55C>T (p.Arg19Trp)
NM_198075.4(LRRC56):c.565A>T (p.Met189Leu)
NM_198075.4(LRRC56):c.602C>T (p.Pro201Leu)
NM_198075.4(LRRC56):c.625G>C (p.Val209Leu)
NM_198075.4(LRRC56):c.650C>T (p.Ala217Val)
NM_198075.4(LRRC56):c.692A>G (p.Glu231Gly)
NM_198075.4(LRRC56):c.716C>T (p.Pro239Leu)
NM_198075.4(LRRC56):c.728C>T (p.Pro243Leu)
NM_198075.4(LRRC56):c.730C>T (p.Arg244Trp)
NM_198075.4(LRRC56):c.740A>G (p.Gln247Arg)
NM_198075.4(LRRC56):c.791C>A (p.Pro264Gln)
NM_198075.4(LRRC56):c.799T>C (p.Cys267Arg)
NM_198075.4(LRRC56):c.820C>T (p.Arg274Trp)
NM_198075.4(LRRC56):c.824G>C (p.Arg275Thr)
NM_198075.4(LRRC56):c.865G>A (p.Ala289Thr)
NM_198075.4(LRRC56):c.886T>A (p.Ser296Thr)
NM_198075.4(LRRC56):c.961A>C (p.Ser321Arg)
NM_198075.4(LRRC56):c.98C>T (p.Pro33Leu)

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