Lrrc34 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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41 records found for search term Lrrc34

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407459722	CV3496871	single nucleotide variant	NM_001172779.2(LRRC34):c.528+1G>A	Autism [RCV004698686]	uncertain significance	3	169806847	169806847	Human	2	name
401742747	CV2697854	single nucleotide variant	NM_001172779.2(LRRC34):c.77G>A (p.Arg26Lys)	not specified [RCV004300566]	uncertain significance	3	169812472	169812472	Human		name
156011263	CV2291126	single nucleotide variant	NM_001172779.2(LRRC34):c.110C>G (p.Thr37Ser)	not specified [RCV004151649]	uncertain significance	3	169812439	169812439	Human		name
401890676	CV2775725	single nucleotide variant	NM_001172779.2(LRRC34):c.255G>T (p.Lys85Asn)	not specified [RCV004350851]	uncertain significance	3	169808630	169808630	Human		name
405655573	CV3277287	single nucleotide variant	NM_001172779.2(LRRC34):c.209C>T (p.Pro70Leu)	not specified [RCV004415440]	uncertain significance	3	169808676	169808676	Human		name
407468141	CV3456448	single nucleotide variant	NM_001172779.2(LRRC34):c.292A>T (p.Asn98Tyr)	not specified [RCV004636166]	uncertain significance	3	169807675	169807675	Human		name
597626134	CV3696813	single nucleotide variant	NM_001172779.2(LRRC34):c.208C>A (p.Pro70Thr)	not specified [RCV004938493]	uncertain significance	3	169808677	169808677	Human		name
8630683	CV85838	single nucleotide variant	NM_001172779.1(LRRC34):c.244G>A (p.Glu82Lys)	Malignant melanoma [RCV000065921]	not provided	3	169808641	169808641	Human		name
34892104	CV906275	single nucleotide variant	NM_001172779.2(LRRC34):c.199A>T (p.Lys67Ter)	Joubert syndrome [RCV001175214]	uncertain significance	3	169808686	169808686	Human	1	name
151880884	CV1406024	single nucleotide variant	NM_001172779.2(LRRC34):c.890G>A (p.Arg297His)	not provided [RCV001941015]	uncertain significance	3	169796763	169796763	Human		name
155963908	CV2194192	single nucleotide variant	NM_001172779.2(LRRC34):c.702C>A (p.Asn234Lys)	not specified [RCV004077273]	uncertain significance	3	169800710	169800710	Human		name
156189290	CV2205927	single nucleotide variant	NM_001172779.2(LRRC34):c.496G>A (p.Glu166Lys)	not specified [RCV004078358]	uncertain significance	3	169806880	169806880	Human		name
156204023	CV2252455	single nucleotide variant	NM_001172779.2(LRRC34):c.363T>A (p.Asn121Lys)	not specified [RCV004116576]	likely benign	3	169807604	169807604	Human		name
156364847	CV2272005	single nucleotide variant	NM_001172779.2(LRRC34):c.733C>T (p.Pro245Ser)	not specified [RCV004124812]	uncertain significance	3	169800679	169800679	Human		name
155906176	CV2283392	single nucleotide variant	NM_001172779.2(LRRC34):c.298C>G (p.Arg100Gly)	not specified [RCV004146038]	uncertain significance	3	169807669	169807669	Human		name
156109047	CV2313913	single nucleotide variant	NM_001172779.2(LRRC34):c.631A>G (p.Lys211Glu)	not specified [RCV004164223]	uncertain significance	3	169804079	169804079	Human		name
156268497	CV2314790	single nucleotide variant	NM_001172779.2(LRRC34):c.764C>T (p.Thr255Ile)	not specified [RCV004170921]	uncertain significance	3	169796889	169796889	Human		name
156171444	CV2317210	single nucleotide variant	NM_001172779.2(LRRC34):c.661A>G (p.Met221Val)	not specified [RCV004176566]	uncertain significance	3	169800751	169800751	Human		name
156188451	CV2342217	single nucleotide variant	NM_001172779.2(LRRC34):c.821G>T (p.Cys274Phe)	not specified [RCV004191798]	uncertain significance	3	169796832	169796832	Human		name
156342784	CV2344097	single nucleotide variant	NM_001172779.2(LRRC34):c.365G>A (p.Cys122Tyr)	not specified [RCV004195701]	uncertain significance	3	169807602	169807602	Human		name
401879180	CV2764884	single nucleotide variant	NM_001172779.2(LRRC34):c.395A>G (p.Tyr132Cys)	not specified [RCV004334977]	uncertain significance	3	169807475	169807475	Human		name
401898357	CV2787721	single nucleotide variant	NM_001172779.2(LRRC34):c.298C>A (p.Arg100Ser)	not specified [RCV004356638]	uncertain significance	3	169807669	169807669	Human		name
405655575	CV3277288	single nucleotide variant	NM_001172779.2(LRRC34):c.535C>T (p.Arg179Trp)	not specified [RCV004415441]	uncertain significance	3	169804175	169804175	Human		name
405655576	CV3277289	single nucleotide variant	NM_001172779.2(LRRC34):c.646G>A (p.Asp216Asn)	not specified [RCV004415442]	uncertain significance	3	169804064	169804064	Human		name
405655578	CV3277290	single nucleotide variant	NM_001172779.2(LRRC34):c.778C>T (p.Arg260Cys)	not specified [RCV004415443]	uncertain significance	3	169796875	169796875	Human		name
405655579	CV3277291	single nucleotide variant	NM_001172779.2(LRRC34):c.809C>T (p.Ala270Val)	not specified [RCV004415444]	likely benign	3	169796844	169796844	Human		name
405655581	CV3277292	single nucleotide variant	NM_001172779.2(LRRC34):c.859T>C (p.Cys287Arg)	not specified [RCV004415445]	uncertain significance	3	169796794	169796794	Human		name
597626147	CV3696807	single nucleotide variant	NM_001172779.2(LRRC34):c.674T>C (p.Ile225Thr)	not specified [RCV004938489]	uncertain significance	3	169800738	169800738	Human		name
597626145	CV3696809	single nucleotide variant	NM_001172779.2(LRRC34):c.736A>C (p.Ile246Leu)	not specified [RCV004938490]	uncertain significance	3	169800676	169800676	Human		name
597626141	CV3696810	single nucleotide variant	NM_001172779.2(LRRC34):c.514G>A (p.Ala172Thr)	not specified [RCV004938491]	uncertain significance	3	169806862	169806862	Human		name
597626138	CV3696812	single nucleotide variant	NM_001172779.2(LRRC34):c.779G>A (p.Arg260His)	not specified [RCV004938492]	likely benign	3	169796874	169796874	Human		name
598272909	CV3988278	single nucleotide variant	NM_001172779.2(LRRC34):c.917T>C (p.Ile306Thr)	not specified [RCV005350590]	uncertain significance	3	169796361	169796361	Human		name
598250819	CV3988280	single nucleotide variant	NM_001172779.2(LRRC34):c.382T>A (p.Leu128Met)	not specified [RCV005366576]	uncertain significance	3	169807488	169807488	Human		name
598272914	CV3988281	single nucleotide variant	NM_001172779.2(LRRC34):c.511A>G (p.Ile171Val)	not specified [RCV005350591]	uncertain significance	3	169806865	169806865	Human		name
156033748	CV2376614	single nucleotide variant	NM_001172779.2(LRRC34):c.1261G>A (p.Asp421Asn)	not specified [RCV004222818]	uncertain significance	3	169793769	169793769	Human		name
156095926	CV2399020	single nucleotide variant	NM_001172779.2(LRRC34):c.1055G>A (p.Ser352Asn)	not specified [RCV004245324]	uncertain significance	3	169796223	169796223	Human		name
401856883	CV2755150	single nucleotide variant	NM_001172779.2(LRRC34):c.1259T>C (p.Val420Ala)	not specified [RCV004335299]	uncertain significance	3	169793771	169793771	Human		name
405655571	CV3277286	single nucleotide variant	NM_001172779.2(LRRC34):c.1270G>A (p.Val424Ile)	not specified [RCV004415439]	uncertain significance	3	169793760	169793760	Human		name
407468136	CV3456447	single nucleotide variant	NM_001172779.2(LRRC34):c.1268G>A (p.Arg423His)	not specified [RCV004636165]	likely benign	3	169793762	169793762	Human		name
597778518	CV3696808	single nucleotide variant	NM_001172779.2(LRRC34):c.1130C>G (p.Thr377Arg)	not specified [RCV004930149]	uncertain significance	3	169795546	169795546	Human		name
598231529	CV3988279	single nucleotide variant	NM_001172779.2(LRRC34):c.1060A>G (p.Lys354Glu)	not specified [RCV005362880]	uncertain significance	3	169796218	169796218	Human		name

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