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12 records found for search term Fabp7
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RGD IDSymbolVariant TypeNameTraitClinical SignificanceChrStartStopSpeciesAnnotationsMatch
15127273CV779138single nucleotide variantNM_001446.5(FABP7):c.348+6T>Cnot provided [RCV000963873]benign6122781200122781200Humanname
15188716CV699290single nucleotide variantNM_001446.5(FABP7):c.288G>A (p.Gln96=)not provided [RCV000953966]benign6122781134122781134Humanname
9850471CV102977deletionNM_001446.5(FABP7):c.239del (p.Asn80fs)not provided [RCV000162281]not provided6122780454122780454Humanname
156019220CV2366899single nucleotide variantNM_001446.5(FABP7):c.71T>C (p.Leu24Pro)not provided [RCV004695706]|not specified [RCV004213312]uncertain significance6122779865122779865Humanname
156180114CV2288067single nucleotide variantNM_001446.5(FABP7):c.253G>A (p.Val85Ile)not specified [RCV004147820]uncertain significance6122781099122781099Humanname
156094296CV2398818single nucleotide variantNM_001446.5(FABP7):c.206A>G (p.Glu69Gly)not specified [RCV004245142]uncertain significance6122780423122780423Humanname
401884184CV2782373single nucleotide variantNM_001446.5(FABP7):c.116C>G (p.Pro39Arg)not specified [RCV004365117]uncertain significance6122780333122780333Humanname
405724126CV3249592single nucleotide variantNM_001446.5(FABP7):c.119C>T (p.Thr40Met)not specified [RCV004378412]uncertain significance6122780336122780336Humanname
405724136CV3249593single nucleotide variantNM_001446.5(FABP7):c.205G>A (p.Glu69Lys)not specified [RCV004378413]uncertain significance6122780422122780422Humanname
597718350CV3671762single nucleotide variantNM_001446.5(FABP7):c.310A>C (p.Asn104His)not specified [RCV004918514]uncertain significance6122781156122781156Humanname
598223362CV3965658single nucleotide variantNM_001446.5(FABP7):c.316G>A (p.Val106Ile)not specified [RCV005341144]uncertain significance6122781162122781162Humanname
598194843CV3965659single nucleotide variantNM_001446.5(FABP7):c.385T>A (p.Tyr129Asn)not specified [RCV005335473]uncertain significance6122783753122783753Humanname