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Variants search result for Homo sapiens
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35 records found for search term Zfp42
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
597726065CV3628080single nucleotide variantNM_174900.5(ZFP42):c.8A>G (p.Gln3Arg)not specified [RCV004888350]uncertain significance4188002815188002815Humanname
156274107CV2334083single nucleotide variantNM_174900.5(ZFP42):c.26C>T (p.Ala9Val)not specified [RCV004183598]uncertain significance4188002833188002833Humanname
597726071CV3628081single nucleotide variantNM_174900.5(ZFP42):c.11A>C (p.Gln4Pro)not specified [RCV004888351]uncertain significance4188002818188002818Humanname
405668855CV3360253single nucleotide variantNM_174900.5(ZFP42):c.89G>A (p.Gly30Asp)not specified [RCV004486060]uncertain significance4188002896188002896Humanname
15172470CV709298single nucleotide variantNM_174900.5(ZFP42):c.774G>A (p.Leu258=)not provided [RCV000972411]benign4188003581188003581Humanname
156176256CV2205312single nucleotide variantNM_174900.5(ZFP42):c.281C>A (p.Ser94Tyr)not specified [RCV004079929]uncertain significance4188003088188003088Humanname
156061140CV2323151single nucleotide variantNM_174900.5(ZFP42):c.187C>G (p.Leu63Val)not specified [RCV004187555]likely benign4188002994188002994Humanname
156256682CV2369168single nucleotide variantNM_174900.5(ZFP42):c.190G>A (p.Gly64Arg)not specified [RCV004208092]uncertain significance4188002997188002997Humanname
156258762CV2395417single nucleotide variantNM_174900.5(ZFP42):c.269C>T (p.Ser90Leu)not specified [RCV004241292]uncertain significance4188003076188003076Humanname
401781668CV2722213single nucleotide variantNM_174900.5(ZFP42):c.253A>G (p.Ile85Val)not specified [RCV004328778]uncertain significance4188003060188003060Humanname
598158897CV3937667single nucleotide variantNM_174900.5(ZFP42):c.124C>T (p.Pro42Ser)not specified [RCV005306445]uncertain significance4188002931188002931Humanname
155923129CV2251856single nucleotide variantNM_174900.5(ZFP42):c.344C>T (p.Ser115Phe)not specified [RCV004119840]uncertain significance4188003151188003151Humanname
155992990CV2252094single nucleotide variantNM_174900.5(ZFP42):c.811G>A (p.Gly271Arg)not specified [RCV004122120]uncertain significance4188003618188003618Humanname
156188689CV2346858single nucleotide variantNM_174900.5(ZFP42):c.832C>T (p.Pro278Ser)not specified [RCV004199855]uncertain significance4188003639188003639Humanname
155907581CV2389922single nucleotide variantNM_174900.5(ZFP42):c.389A>G (p.Glu130Gly)not specified [RCV004236131]uncertain significance4188003196188003196Humanname
156260883CV2395582single nucleotide variantNM_174900.5(ZFP42):c.562A>G (p.Ile188Val)not specified [RCV004241433]uncertain significance4188003369188003369Humanname
329382640CV2449277single nucleotide variantNM_174900.5(ZFP42):c.788G>A (p.Arg263His)not specified [RCV004257411]uncertain significance4188003595188003595Humanname
329357688CV2453747single nucleotide variantNM_174900.5(ZFP42):c.855G>T (p.Arg285Ser)not specified [RCV004269379]uncertain significance4188003662188003662Humanname
405668839CV3360250single nucleotide variantNM_174900.5(ZFP42):c.517A>G (p.Arg173Gly)not specified [RCV004486057]uncertain significance4188003324188003324Humanname
405668842CV3360251single nucleotide variantNM_174900.5(ZFP42):c.520A>C (p.Lys174Gln)not specified [RCV004486058]uncertain significance4188003327188003327Humanname
405668850CV3360252single nucleotide variantNM_174900.5(ZFP42):c.841G>A (p.Gly281Ser)not specified [RCV004486059]uncertain significance4188003648188003648Humanname
407457950CV3490136single nucleotide variantNM_174900.5(ZFP42):c.752G>A (p.Gly251Glu)not specified [RCV004686515]uncertain significance4188003559188003559Humanname
597726050CV3628075single nucleotide variantNM_174900.5(ZFP42):c.757G>A (p.Gly253Arg)not specified [RCV004888348]uncertain significance4188003564188003564Humanname
597726057CV3628076single nucleotide variantNM_174900.5(ZFP42):c.709C>G (p.Leu237Val)not specified [RCV004888349]uncertain significance4188003516188003516Humanname
597794267CV3628077single nucleotide variantNM_174900.5(ZFP42):c.698A>C (p.Lys233Thr)not specified [RCV004877591]uncertain significance4188003505188003505Humanname
597794270CV3628078single nucleotide variantNM_174900.5(ZFP42):c.628C>T (p.Leu210Phe)not specified [RCV004877592]uncertain significance4188003435188003435Humanname
597794273CV3628079single nucleotide variantNM_174900.5(ZFP42):c.736C>T (p.Arg246Trp)not specified [RCV004877593]uncertain significance4188003543188003543Humanname
598158893CV3937665single nucleotide variantNM_174900.5(ZFP42):c.334G>A (p.Glu112Lys)not specified [RCV005306444]uncertain significance4188003141188003141Humanname
598259454CV3937666single nucleotide variantNM_174900.5(ZFP42):c.850A>T (p.Arg284Trp)not specified [RCV005300229]uncertain significance4188003657188003657Humanname
598259459CV3937668single nucleotide variantNM_174900.5(ZFP42):c.764G>A (p.Arg255His)not specified [RCV005300230]uncertain significance4188003571188003571Humanname
598158902CV3937670single nucleotide variantNM_174900.5(ZFP42):c.386A>G (p.Lys129Arg)not specified [RCV005306446]uncertain significance4188003193188003193Humanname
598259466CV3937671single nucleotide variantNM_174900.5(ZFP42):c.387A>C (p.Lys129Asn)not specified [RCV005300232]uncertain significance4188003194188003194Humanname
598158907CV3937672single nucleotide variantNM_174900.5(ZFP42):c.756C>G (p.Cys252Trp)not specified [RCV005306447]uncertain significance4188003563188003563Humanname
15158331CV709297single nucleotide variantNM_174900.5(ZFP42):c.737G>T (p.Arg246Leu)not provided [RCV000969487]likely benign4188003544188003544Humanname
8625758CV80882deletionNM_174900.4(ZFP42):c.375delA (p.Val127Terfs)Malignant melanoma [RCV000060959]not provided4188003182188003182Humanname