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14 records found for search term Atg12
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
156329471CV2216419single nucleotide variantNM_004707.4(ATG12):c.22G>C (p.Val8Leu)not specified [RCV004097250]uncertain significance5115841531115841531Humanname
407494519CV3477655single nucleotide variantNM_004707.4(ATG12):c.17A>C (p.Gln6Pro)not specified [RCV004667660]uncertain significance5115841536115841536Humanname
597675539CV3599651single nucleotide variantNM_004707.4(ATG12):c.14C>T (p.Pro5Leu)not specified [RCV004856870]uncertain significance5115841539115841539Humanname
597675640CV3599662single nucleotide variantNM_004707.4(ATG12):c.65T>G (p.Leu22Arg)not specified [RCV004856881]uncertain significance5115841488115841488Humanname
597675738CV3599673single nucleotide variantNM_004707.4(ATG12):c.31C>G (p.Leu11Val)not specified [RCV004856892]uncertain significance5115841522115841522Humanname
405688638CV3279758single nucleotide variantNM_004707.4(ATG12):c.169A>G (p.Ile57Val)not specified [RCV004423257]uncertain significance5115837759115837759Humanname
597675749CV3596223single nucleotide variantNM_004707.4(ATG12):c.139C>T (p.Pro47Ser)not specified [RCV004856900]uncertain significance5115841414115841414Humanname
598259043CV3911000single nucleotide variantNM_004707.4(ATG12):c.155A>G (p.Lys52Arg)not specified [RCV005279504]uncertain significance5115841398115841398Humanname
598259094CV3911011single nucleotide variantNM_004707.4(ATG12):c.223G>A (p.Val75Ile)not specified [RCV005279513]uncertain significance5115837705115837705Humanname
598267349CV3911027single nucleotide variantNM_004707.4(ATG12):c.124C>G (p.Pro42Ala)not specified [RCV005281565]uncertain significance5115841429115841429Humanname
156081840CV2205389single nucleotide variantNM_004707.4(ATG12):c.304A>G (p.Ile102Val)not specified [RCV004082337]uncertain significance5115832661115832661Humanname
597675867CV3596234single nucleotide variantNM_004707.4(ATG12):c.341A>G (p.Gln114Arg)not specified [RCV004856911]uncertain significance5115832624115832624Humanname
597675981CV3596245single nucleotide variantNM_004707.4(ATG12):c.359A>C (p.Tyr120Ser)not specified [RCV004856922]uncertain significance5115832606115832606Humanname
598267320CV3911021single nucleotide variantNM_004707.4(ATG12):c.320C>G (p.Ser107Cys)not specified [RCV005281560]uncertain significance5115832645115832645Humanname