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19 records found for search term Klk6
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
405813964CV3276431single nucleotide variantNM_002774.4(KLK6):c.52G>A (p.Glu18Lys)not specified [RCV004409667]uncertain significance195096731450967314Humanname
597797191CV3700913single nucleotide variantNM_002774.4(KLK6):c.76G>A (p.Gly26Arg)not specified [RCV004935723]uncertain significance195096729050967290Humanname
598183143CV3983844single nucleotide variantNM_002774.4(KLK6):c.85G>A (p.Asp29Asn)not specified [RCV005352849]uncertain significance195096728150967281Humanname
598161930CV3983847single nucleotide variantNM_002774.4(KLK6):c.76G>C (p.Gly26Arg)not specified [RCV005368534]uncertain significance195096729050967290Humanname
156384978CV2371662single nucleotide variantNM_002774.4(KLK6):c.248C>T (p.Ser83Phe)not specified [RCV004216901]likely benign195096349950963499Humanname
329385857CV2428125single nucleotide variantNM_002774.4(KLK6):c.271C>T (p.Arg91Trp)not specified [RCV004251167]uncertain significance195096347650963476Humanname
598161936CV3983848single nucleotide variantNM_002774.4(KLK6):c.265G>C (p.Val89Leu)not specified [RCV005368535]uncertain significance195096348250963482Humanname
15120661CV716634single nucleotide variantNM_002774.4(KLK6):c.232C>T (p.Arg78Trp)not provided [RCV000962757]benign195096351550963515Humanname
156172937CV2194304single nucleotide variantNM_002774.4(KLK6):c.649C>T (p.Pro217Ser)not specified [RCV004079420]uncertain significance195095925050959250Humanname
156148854CV2265307single nucleotide variantNM_002774.4(KLK6):c.641G>A (p.Gly214Asp)not specified [RCV004128199]uncertain significance195095925850959258Humanname
155910468CV2369948single nucleotide variantNM_002774.4(KLK6):c.346G>A (p.Ala116Thr)not specified [RCV004208413]uncertain significance195096340150963401Humanname
329372543CV2443161single nucleotide variantNM_002774.4(KLK6):c.380T>C (p.Leu127Pro)not specified [RCV004255356]uncertain significance195096336750963367Humanname
329385414CV2451378single nucleotide variantNM_002774.4(KLK6):c.714A>T (p.Gln238His)not specified [RCV004272065]uncertain significance195095918550959185Humanname
329386434CV2456005single nucleotide variantNM_002774.4(KLK6):c.590C>T (p.Ser197Phe)not specified [RCV004272912]uncertain significance195095930950959309Humanname
597797195CV3700914single nucleotide variantNM_002774.4(KLK6):c.377C>T (p.Pro126Leu)not specified [RCV004935724]uncertain significance195096337050963370Humanname
597797198CV3700915single nucleotide variantNM_002774.4(KLK6):c.467A>G (p.Gln156Arg)not specified [RCV004935725]uncertain significance195096185950961859Humanname
597797201CV3700916single nucleotide variantNM_002774.4(KLK6):c.337G>A (p.Ala113Thr)not specified [RCV004935726]uncertain significance195096341050963410Humanname
597769416CV3700917single nucleotide variantNM_002774.4(KLK6):c.301G>A (p.Ala101Thr)not specified [RCV004927589]uncertain significance195096344650963446Humanname
598221514CV3983845single nucleotide variantNM_002774.4(KLK6):c.302C>T (p.Ala101Val)not specified [RCV005360816]uncertain significance195096344550963445Humanname