ClinVar Miner

List of variants in gene NDUFAF6 reported as uncertain significance for not provided

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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_152416.4(NDUFAF6):c.641T>C (p.Val214Ala) rs376835502 0.00056
NM_152416.4(NDUFAF6):c.715-3C>A rs200620409 0.00054
NM_152416.4(NDUFAF6):c.773T>C (p.Val258Ala) rs745941126 0.00017
NM_152416.4(NDUFAF6):c.404C>T (p.Ala135Val) rs763634041 0.00007
NM_152416.4(NDUFAF6):c.779A>G (p.Tyr260Cys) rs746347617 0.00007
NM_152416.4(NDUFAF6):c.458T>C (p.Met153Thr) rs765194083 0.00006
NM_152416.4(NDUFAF6):c.326T>C (p.Ile109Thr) rs372565148 0.00005
NM_152416.4(NDUFAF6):c.383A>G (p.Asn128Ser) rs375665080 0.00005
NM_152416.4(NDUFAF6):c.298-768T>C rs575462405 0.00004
NM_152416.4(NDUFAF6):c.532G>C (p.Ala178Pro) rs201088736 0.00004
NM_152416.4(NDUFAF6):c.743G>A (p.Arg248Gln) rs569186576 0.00002
NM_152416.4(NDUFAF6):c.398C>T (p.Pro133Leu) rs906392027 0.00001
NM_152416.4(NDUFAF6):c.505C>T (p.Arg169Cys) rs762805477 0.00001
NM_152416.4(NDUFAF6):c.557_559del (p.Leu186_Tyr187delinsHis) rs753367800 0.00001
NM_152416.4(NDUFAF6):c.665A>G (p.Tyr222Cys) rs375090043 0.00001
NM_152416.4(NDUFAF6):c.709A>T (p.Met237Leu) rs761183883 0.00001
NM_152416.4(NDUFAF6):c.725C>T (p.Ser242Leu) rs753297390 0.00001
NM_152416.4(NDUFAF6):c.808C>G (p.Leu270Val) rs747954437 0.00001
NC_000008.10:g.(?_96037237)_(96070165_?)dup
NC_000008.10:g.(?_96070017)_(96070165_?)del
NM_152416.4(NDUFAF6):c.233_242dup (p.Glu82fs) rs863223932
NM_152416.4(NDUFAF6):c.239C>G (p.Pro80Arg) rs1828914859
NM_152416.4(NDUFAF6):c.275C>T (p.Ala92Val)
NM_152416.4(NDUFAF6):c.297+7A>G
NM_152416.4(NDUFAF6):c.316G>A (p.Glu106Lys) rs2131806805
NM_152416.4(NDUFAF6):c.319A>C (p.Lys107Gln) rs767438662
NM_152416.4(NDUFAF6):c.406A>G (p.Ile136Val)
NM_152416.4(NDUFAF6):c.428A>G (p.Lys143Arg)
NM_152416.4(NDUFAF6):c.466G>A (p.Val156Ile)
NM_152416.4(NDUFAF6):c.499G>A (p.Ala167Thr) rs2131886983
NM_152416.4(NDUFAF6):c.505C>G (p.Arg169Gly)
NM_152416.4(NDUFAF6):c.513C>G (p.Ile171Met)
NM_152416.4(NDUFAF6):c.553C>T (p.Leu185Phe)
NM_152416.4(NDUFAF6):c.576A>G (p.Ile192Met)
NM_152416.4(NDUFAF6):c.591T>A (p.Asp197Glu)
NM_152416.4(NDUFAF6):c.619A>G (p.Ile207Val)
NM_152416.4(NDUFAF6):c.655G>A (p.Ala219Thr)
NM_152416.4(NDUFAF6):c.690C>G (p.Phe230Leu) rs199955582
NM_152416.4(NDUFAF6):c.694C>A (p.Pro232Thr)
NM_152416.4(NDUFAF6):c.743G>C (p.Arg248Pro) rs569186576
NM_152416.4(NDUFAF6):c.803T>C (p.Leu268Ser) rs1831069873
NM_152416.4(NDUFAF6):c.805C>T (p.His269Tyr)
NM_152416.4(NDUFAF6):c.842del (p.Pro281fs) rs746736083
NM_152416.4(NDUFAF6):c.850G>A (p.Ala284Thr) rs1831515972
NM_152416.4(NDUFAF6):c.872C>A (p.Thr291Lys) rs763178410
NM_152416.4(NDUFAF6):c.872C>T (p.Thr291Met)
NM_152416.4(NDUFAF6):c.874G>T (p.Val292Phe) rs368684155
NM_152416.4(NDUFAF6):c.908G>A (p.Arg303Gln)
NM_152416.4(NDUFAF6):c.962C>G (p.Pro321Arg)
NM_152416.4(NDUFAF6):c.967del (p.Tyr323fs)

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