Fads1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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14 records found for search term Fads1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
598223404	CV3965665	single nucleotide variant	NM_013402.7(FADS1):c.11G>A (p.Arg4His)	not specified [RCV005341150]	uncertain significance	11	61816919	61816919	Human		name
15122915	CV774310	single nucleotide variant	NM_013402.7(FADS1):c.186G>T (p.Pro62=)	not provided [RCV000940761]	likely benign	11	61816744	61816744	Human		name
38467362	CV920832	single nucleotide variant	NM_013402.7(FADS1):c.141T>G (p.Ala47=)	not provided [RCV001200346]	likely benign	11	61816789	61816789	Human		name
405724170	CV3249597	single nucleotide variant	NM_013402.7(FADS1):c.83G>A (p.Arg28His)	not specified [RCV004378417]	uncertain significance	11	61816847	61816847	Human		name
156343440	CV2353464	single nucleotide variant	NM_013402.7(FADS1):c.116C>G (p.Pro39Arg)	not specified [RCV004205918]	uncertain significance	11	61816814	61816814	Human		name
598223412	CV3965666	single nucleotide variant	NM_013402.7(FADS1):c.181G>A (p.Asp61Asn)	not specified [RCV005341151]	uncertain significance	11	61816749	61816749	Human		name
155942233	CV2229517	single nucleotide variant	NM_013402.7(FADS1):c.664G>T (p.Val222Leu)	not specified [RCV004103058]	uncertain significance	11	61812491	61812491	Human		name
155928398	CV2391725	single nucleotide variant	NM_013402.7(FADS1):c.533G>A (p.Arg178Gln)	not specified [RCV004241878]	likely benign	11	61812622	61812622	Human		name
401879256	CV2774536	single nucleotide variant	NM_013402.7(FADS1):c.532C>T (p.Arg178Trp)	not specified [RCV004350021]	uncertain significance	11	61812623	61812623	Human		name
597718369	CV3671765	single nucleotide variant	NM_013402.7(FADS1):c.851G>A (p.Arg284His)	not specified [RCV004918516]	uncertain significance	11	61810815	61810815	Human		name
598223389	CV3965663	single nucleotide variant	NM_013402.7(FADS1):c.556C>T (p.His186Tyr)	not specified [RCV005341148]	uncertain significance	11	61812599	61812599	Human		name
598223397	CV3965664	single nucleotide variant	NM_013402.7(FADS1):c.662C>T (p.Ala221Val)	not specified [RCV005341149]	uncertain significance	11	61812493	61812493	Human		name
156184121	CV2294853	single nucleotide variant	NM_013402.7(FADS1):c.1416G>T (p.Gln472His)	not specified [RCV004156014]	uncertain significance	11	61802839	61802839	Human		name
407501007	CV3435344	single nucleotide variant	NM_013402.7(FADS1):c.1191G>T (p.Met397Ile)	not specified [RCV004623166]	uncertain significance	11	61803420	61803420	Human		name