Il17d Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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26 records found for search term Il17d

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15112352	CV753748	single nucleotide variant	NM_001385224.1(IL17D):c.112C>T (p.Leu38=)	not provided [RCV000916895]	likely benign	13	20704113	20704113	Human		name
155968216	CV2312808	single nucleotide variant	NM_001385224.1(IL17D):c.76G>A (p.Ala26Thr)	not specified [RCV004169519]	uncertain significance	13	20704077	20704077	Human		name
156064285	CV2340750	single nucleotide variant	NM_001385224.1(IL17D):c.77C>T (p.Ala26Val)	not specified [RCV004188114]	uncertain significance	13	20704078	20704078	Human		name
401748156	CV2698943	single nucleotide variant	NM_001385224.1(IL17D):c.80G>C (p.Arg27Pro)	not specified [RCV004303479]	uncertain significance	13	20704081	20704081	Human		name
15147256	CV713865	single nucleotide variant	NM_001385224.1(IL17D):c.366G>C (p.Gly122=)	not provided [RCV000967305]	benign	13	20721711	20721711	Human		name
15199180	CV753749	single nucleotide variant	NM_001385224.1(IL17D):c.339C>T (p.Tyr113=)	not provided [RCV000912473]	likely benign	13	20721684	20721684	Human		name
156290473	CV2226181	single nucleotide variant	NM_001385224.1(IL17D):c.280T>C (p.Trp94Arg)	not specified [RCV004105582]	uncertain significance	13	20704281	20704281	Human		name
156159100	CV2398085	single nucleotide variant	NM_001385224.1(IL17D):c.196G>C (p.Ala66Pro)	not specified [RCV004241672]	uncertain significance	13	20704197	20704197	Human		name
329376295	CV2425061	single nucleotide variant	NM_001385224.1(IL17D):c.148G>A (p.Val50Met)	not specified [RCV004248957]	uncertain significance	13	20704149	20704149	Human		name
329365899	CV2441214	single nucleotide variant	NM_001385224.1(IL17D):c.254C>T (p.Pro85Leu)	not specified [RCV004263607]	uncertain significance	13	20704255	20704255	Human		name
405804488	CV3270944	single nucleotide variant	NM_001385224.1(IL17D):c.212G>C (p.Cys71Ser)	not specified [RCV004405005]	uncertain significance	13	20704213	20704213	Human		name
405804490	CV3270945	single nucleotide variant	NM_001385224.1(IL17D):c.238C>T (p.Arg80Cys)	not specified [RCV004405006]	uncertain significance	13	20704239	20704239	Human		name
597793213	CV3690202	single nucleotide variant	NM_001385224.1(IL17D):c.100C>G (p.Arg34Gly)	not specified [RCV004934046]	uncertain significance	13	20704101	20704101	Human		name
598179464	CV3972108	single nucleotide variant	NM_001385224.1(IL17D):c.109G>A (p.Glu37Lys)	not specified [RCV005352162]	uncertain significance	13	20704110	20704110	Human		name
156343937	CV2229569	single nucleotide variant	NM_001385224.1(IL17D):c.553G>C (p.Asp185His)	not specified [RCV004103391]	uncertain significance	13	20721898	20721898	Human		name
401747477	CV2696710	single nucleotide variant	NM_001385224.1(IL17D):c.565G>A (p.Ala189Thr)	not specified [RCV004290686]	uncertain significance	13	20721910	20721910	Human		name
401730777	CV2711489	single nucleotide variant	NM_001385224.1(IL17D):c.301G>C (p.Asp101His)	not specified [RCV004306806]	uncertain significance	13	20721646	20721646	Human		name
401738379	CV2711835	single nucleotide variant	NM_001385224.1(IL17D):c.385G>A (p.Val129Met)	not specified [RCV004309469]	uncertain significance	13	20721730	20721730	Human		name
401859630	CV2771750	single nucleotide variant	NM_001385224.1(IL17D):c.313T>C (p.Tyr105His)	not specified [RCV004350530]	uncertain significance	13	20721658	20721658	Human		name
405804492	CV3270946	single nucleotide variant	NM_001385224.1(IL17D):c.361A>G (p.Thr121Ala)	not specified [RCV004405007]	uncertain significance	13	20721706	20721706	Human		name
405804494	CV3270947	single nucleotide variant	NM_001385224.1(IL17D):c.437C>G (p.Thr146Ser)	not specified [RCV004405008]	uncertain significance	13	20721782	20721782	Human		name
405804496	CV3270948	single nucleotide variant	NM_001385224.1(IL17D):c.571C>G (p.Leu191Val)	not specified [RCV004405009]	uncertain significance	13	20721916	20721916	Human		name
597793210	CV3690203	single nucleotide variant	NM_001385224.1(IL17D):c.341G>A (p.Cys114Tyr)	not specified [RCV004934047]	uncertain significance	13	20721686	20721686	Human		name
598179452	CV3972106	single nucleotide variant	NM_001385224.1(IL17D):c.395G>T (p.Arg132Leu)	not specified [RCV005352160]	uncertain significance	13	20721740	20721740	Human		name
598179459	CV3972107	single nucleotide variant	NM_001385224.1(IL17D):c.587A>G (p.Asn196Ser)	not specified [RCV005352161]	uncertain significance	13	20721932	20721932	Human		name
15200847	CV725417	single nucleotide variant	NM_001385224.1(IL17D):c.552C>G (p.Ile184Met)	not provided [RCV000891025]	benign	13	20721897	20721897	Human		name

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