Hopx Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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18 records found for search term Hopx

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
155923483	CV2215668	single nucleotide variant	NM_032495.6(HOPX):c.199-1954G>T	not specified [RCV004091200]	likely benign	4	56650751	56650751	Human		name
155977837	CV2321279	single nucleotide variant	NM_032495.6(HOPX):c.199-1995G>C	not specified [RCV004175390]	uncertain significance	4	56650792	56650792	Human		name
405791614	CV3263260	single nucleotide variant	NM_032495.6(HOPX):c.199-2015G>T	not specified [RCV004399917]	uncertain significance	4	56650812	56650812	Human		name
597772214	CV3679559	single nucleotide variant	NM_032495.6(HOPX):c.199-2011G>A	not specified [RCV004928630]	uncertain significance	4	56650808	56650808	Human		name
8610746	CV57044	single nucleotide variant	NM_032495.6(HOPX):c.87G>A (p.Glu29=)	not provided [RCV004715652]\|not specified [RCV000041150]	benign\|likely benign\|conflicting interpretations of pathogenicity	4	56655968	56655968	Human		name
34895790	CV916927	single nucleotide variant	NM_032495.6(HOPX):c.264C>T (p.Ser88=)	not specified [RCV001192973]	benign	4	56648732	56648732	Human		name
155969704	CV2337982	single nucleotide variant	NM_032495.6(HOPX):c.43C>G (p.Arg15Gly)	not specified [RCV004186026]	uncertain significance	4	56656012	56656012	Human		name
156185197	CV2346499	single nucleotide variant	NM_032495.6(HOPX):c.88G>T (p.Asp30Tyr)	not specified [RCV004206422]	uncertain significance	4	56655967	56655967	Human		name
401872901	CV2793013	single nucleotide variant	NM_032495.6(HOPX):c.80C>G (p.Pro27Arg)	not specified [RCV004360349]	uncertain significance	4	56655975	56655975	Human		name
407527994	CV3433765	single nucleotide variant	NM_032495.6(HOPX):c.55A>G (p.Met19Val)	not specified [RCV004632977]	uncertain significance	4	56656000	56656000	Human		name
597772209	CV3679558	single nucleotide variant	NM_032495.6(HOPX):c.56T>C (p.Met19Thr)	not specified [RCV004928629]	uncertain significance	4	56655999	56655999	Human		name
155960223	CV2204131	single nucleotide variant	NM_032495.6(HOPX):c.143C>T (p.Ser48Phe)	not specified [RCV004076939]	uncertain significance	4	56655912	56655912	Human		name
401863017	CV2775568	single nucleotide variant	NM_032495.6(HOPX):c.131A>G (p.Lys44Arg)	not specified [RCV004350736]	uncertain significance	4	56655924	56655924	Human		name
597772218	CV3679560	single nucleotide variant	NM_032495.6(HOPX):c.146C>A (p.Thr49Asn)	not specified [RCV004928631]	uncertain significance	4	56655909	56655909	Human		name
598191430	CV3975599	single nucleotide variant	NM_032495.6(HOPX):c.185A>G (p.Glu62Gly)	not specified [RCV005354280]	uncertain significance	4	56655870	56655870	Human		name
13520269	CV487016	single nucleotide variant	NM_032495.6(HOPX):c.167C>T (p.Ala56Val)	not provided [RCV000587478]	likely benign	4	56655888	56655888	Human		name
13521338	CV487097	single nucleotide variant	NM_032495.6(HOPX):c.215G>A (p.Arg72His)	not provided [RCV000589152]	likely benign	4	56648781	56648781	Human		name
8610747	CV57045	single nucleotide variant	NM_032495.6(HOPX):c.124G>A (p.Val42Ile)	not specified [RCV000041151]	uncertain significance	4	56655931	56655931	Human		name