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Variants search result for Homo sapiens
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36 records found for search term Igsf6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
401885074CV2771200single nucleotide variantNM_005849.4(IGSF6):c.5G>A (p.Gly2Glu)not specified [RCV004346188]likely benign162165259421652594Humanname
401898597CV2788012single nucleotide variantNM_005849.4(IGSF6):c.21C>A (p.Ser7Arg)not specified [RCV004358665]uncertain significance162165257821652578Humanname
156133203CV2365981single nucleotide variantNM_005849.4(IGSF6):c.62G>A (p.Cys21Tyr)not specified [RCV004207586]likely benign162165253721652537Humanname
401721457CV2709970single nucleotide variantNM_005849.4(IGSF6):c.71C>T (p.Ala24Val)not specified [RCV004315038]uncertain significance162164748921647489Humanname
401898574CV2788013single nucleotide variantNM_005849.4(IGSF6):c.28G>A (p.Ala10Thr)not specified [RCV004358666]uncertain significance162165257121652571Humanname
597792591CV3690021single nucleotide variantNM_005849.4(IGSF6):c.44C>A (p.Thr15Asn)not specified [RCV004933893]uncertain significance162165255521652555Humanname
598207140CV3975908single nucleotide variantNM_005849.4(IGSF6):c.32G>A (p.Arg11His)not specified [RCV005337925]uncertain significance162165256721652567Humanname
598207145CV3975912single nucleotide variantNM_005849.4(IGSF6):c.53T>C (p.Ile18Thr)not specified [RCV005337926]uncertain significance162165254621652546Humanname
155932959CV2228772single nucleotide variantNM_005849.4(IGSF6):c.104C>T (p.Pro35Leu)not specified [RCV004093239]uncertain significance162164745621647456Humanname
405800060CV3274671single nucleotide variantNM_005849.4(IGSF6):c.143C>T (p.Thr48Ile)not specified [RCV004402809]uncertain significance162164741721647417Humanname
405800062CV3274672single nucleotide variantNM_005849.4(IGSF6):c.214G>T (p.Ala72Ser)not specified [RCV004402810]uncertain significance162164734621647346Humanname
407479542CV3440902single nucleotide variantNM_005849.4(IGSF6):c.263A>C (p.Asp88Ala)not specified [RCV004627874]uncertain significance162164729721647297Humanname
407479546CV3440903single nucleotide variantNM_005849.4(IGSF6):c.115G>C (p.Glu39Gln)not specified [RCV004627875]uncertain significance162164744521647445Humanname
597792602CV3690025single nucleotide variantNM_005849.4(IGSF6):c.108G>T (p.Trp36Cys)not specified [RCV004933897]uncertain significance162164745221647452Humanname
597792605CV3690026single nucleotide variantNM_005849.4(IGSF6):c.206G>A (p.Arg69His)not specified [RCV004933898]uncertain significance162164735421647354Humanname
598207150CV3975914single nucleotide variantNM_005849.4(IGSF6):c.254G>C (p.Ser85Thr)not specified [RCV005337927]uncertain significance162164730621647306Humanname
598269875CV3975915single nucleotide variantNM_005849.4(IGSF6):c.167C>T (p.Thr56Ile)not specified [RCV005349989]uncertain significance162164739321647393Humanname
156276734CV2209806single nucleotide variantNM_005849.4(IGSF6):c.497T>C (p.Val166Ala)not specified [RCV004076274]uncertain significance162164432721644327Humanname
156327198CV2217219single nucleotide variantNM_005849.4(IGSF6):c.602G>A (p.Arg201His)not specified [RCV004087673]uncertain significance162164313821643138Humanname
156185244CV2324648single nucleotide variantNM_005849.4(IGSF6):c.698G>T (p.Arg233Ile)not specified [RCV004172897]uncertain significance162164156221641562Humanname
329397696CV2463918single nucleotide variantNM_005849.4(IGSF6):c.392A>G (p.Lys131Arg)not specified [RCV004279985]uncertain significance162164716821647168Humanname
401761440CV2726767single nucleotide variantNM_005849.4(IGSF6):c.635A>G (p.His212Arg)not specified [RCV004323086]uncertain significance162164310521643105Humanname
401764647CV2728017single nucleotide variantNM_005849.4(IGSF6):c.548C>T (p.Pro183Leu)not specified [RCV004324146]uncertain significance162164358521643585Humanname
405800115CV3274673single nucleotide variantNM_005849.4(IGSF6):c.511G>A (p.Val171Met)not specified [RCV004402811]uncertain significance162164431321644313Humanname
405800117CV3274674single nucleotide variantNM_005849.4(IGSF6):c.532A>G (p.Lys178Glu)not specified [RCV004402812]uncertain significance162164429221644292Humanname
405800119CV3274675single nucleotide variantNM_005849.4(IGSF6):c.550C>A (p.Leu184Ile)not specified [RCV004402813]uncertain significance162164358321643583Humanname
405800121CV3274676single nucleotide variantNM_005849.4(IGSF6):c.588G>C (p.Lys196Asn)not specified [RCV004402814]uncertain significance162164315221643152Humanname
407479531CV3440900single nucleotide variantNM_005849.4(IGSF6):c.470C>T (p.Ala157Val)not specified [RCV004627872]uncertain significance162164435421644354Humanname
407479537CV3440901single nucleotide variantNM_005849.4(IGSF6):c.717A>T (p.Glu239Asp)not specified [RCV004627873]uncertain significance162164154321641543Humanname
597792594CV3690022single nucleotide variantNM_005849.4(IGSF6):c.496G>A (p.Val166Met)not specified [RCV004933894]uncertain significance162164432821644328Humanname
597792597CV3690023single nucleotide variantNM_005849.4(IGSF6):c.588G>T (p.Lys196Asn)not specified [RCV004933895]uncertain significance162164315221643152Humanname
597792599CV3690024single nucleotide variantNM_005849.4(IGSF6):c.657T>A (p.Asn219Lys)not specified [RCV004933896]uncertain significance162164308321643083Humanname
598269855CV3975909single nucleotide variantNM_005849.4(IGSF6):c.502G>A (p.Gly168Ser)not specified [RCV005349985]uncertain significance162164432221644322Humanname
598269865CV3975911single nucleotide variantNM_005849.4(IGSF6):c.377C>T (p.Pro126Leu)not specified [RCV005349987]uncertain significance162164718321647183Humanname
598269870CV3975913single nucleotide variantNM_005849.4(IGSF6):c.494A>G (p.Tyr165Cys)not specified [RCV005349988]uncertain significance162164433021644330Humanname
598269880CV3975916single nucleotide variantNM_005849.4(IGSF6):c.425G>A (p.Arg142Lys)not specified [RCV005349990]uncertain significance162164713521647135Humanname