Cpa2 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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43 records found for search term Cpa2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15114579	CV750423	single nucleotide variant	NM_001869.3(CPA2):c.198C>T (p.His66=)	not provided [RCV000917302]	benign	7	130269713	130269713	Human		name
156034919	CV2246636	single nucleotide variant	NM_001869.3(CPA2):c.44A>G (p.His15Arg)	not specified [RCV004110376]	uncertain significance	7	130266925	130266925	Human		name
156178118	CV2229260	single nucleotide variant	NM_001869.3(CPA2):c.251A>G (p.Gln84Arg)	not specified [RCV004101069]	uncertain significance	7	130269766	130269766	Human		name
156175733	CV2374397	single nucleotide variant	NM_001869.3(CPA2):c.214G>A (p.Val72Ile)	not specified [RCV004231916]	uncertain significance	7	130269729	130269729	Human		name
401730397	CV2680298	single nucleotide variant	NM_001869.3(CPA2):c.283G>A (p.Val95Met)	not specified [RCV004288551]	uncertain significance	7	130269798	130269798	Human		name
597650096	CV3650914	single nucleotide variant	NM_001869.3(CPA2):c.133G>A (p.Glu45Lys)	not specified [RCV004910422]	uncertain significance	7	130268990	130268990	Human		name
15136343	CV710768	single nucleotide variant	NM_001869.3(CPA2):c.199G>A (p.Val67Ile)	not provided [RCV000965439]	benign	7	130269714	130269714	Human		name
8632336	CV87544	single nucleotide variant	NM_001869.2(CPA2):c.202C>T (p.Arg68Ter)	Malignant melanoma [RCV000067635]	not provided	7	130269717	130269717	Human		name
156243651	CV2210981	single nucleotide variant	NM_001869.3(CPA2):c.877A>G (p.Ile293Val)	not specified [RCV004086049]	uncertain significance	7	130279552	130279552	Human		name
156381546	CV2215612	single nucleotide variant	NM_001869.3(CPA2):c.598T>C (p.Tyr200His)	not specified [RCV004089369]	uncertain significance	7	130276640	130276640	Human		name
156388594	CV2231910	single nucleotide variant	NM_001869.3(CPA2):c.515T>C (p.Ile172Thr)	not specified [RCV004098699]	uncertain significance	7	130275177	130275177	Human		name
155944059	CV2241865	single nucleotide variant	NM_001869.3(CPA2):c.719G>C (p.Arg240Pro)	not specified [RCV004106787]	uncertain significance	7	130277848	130277848	Human		name
156251681	CV2311313	single nucleotide variant	NM_001869.3(CPA2):c.409G>A (p.Val137Met)	not specified [RCV004166386]	uncertain significance	7	130273100	130273100	Human		name
155927981	CV2349901	single nucleotide variant	NM_001869.3(CPA2):c.424G>T (p.Gly142Cys)	not specified [RCV004206316]	uncertain significance	7	130273115	130273115	Human		name
156137126	CV2365130	single nucleotide variant	NM_001869.3(CPA2):c.726G>T (p.Lys242Asn)	not specified [RCV004224284]	uncertain significance	7	130277855	130277855	Human		name
156033128	CV2376559	single nucleotide variant	NM_001869.3(CPA2):c.434G>A (p.Ser145Asn)	not specified [RCV004220723]	uncertain significance	7	130273125	130273125	Human		name
155994398	CV2379539	single nucleotide variant	NM_001869.3(CPA2):c.405C>G (p.Asn135Lys)	not specified [RCV004217248]	uncertain significance	7	130273096	130273096	Human		name
329385187	CV2454796	single nucleotide variant	NM_001869.3(CPA2):c.701G>A (p.Arg234His)	not specified [RCV004270019]	uncertain significance	7	130277830	130277830	Human		name
329371702	CV2454850	single nucleotide variant	NM_001869.3(CPA2):c.533T>C (p.Ile178Thr)	not specified [RCV004270355]	uncertain significance	7	130275195	130275195	Human		name
329382721	CV2465341	single nucleotide variant	NM_001869.3(CPA2):c.305A>T (p.Glu102Val)	not specified [RCV004281127]	uncertain significance	7	130270709	130270709	Human		name
401771243	CV2675512	single nucleotide variant	NM_001869.3(CPA2):c.443A>T (p.Asn148Ile)	not specified [RCV004295129]	uncertain significance	7	130273134	130273134	Human		name
401752301	CV2706829	single nucleotide variant	NM_001869.3(CPA2):c.619A>G (p.Thr207Ala)	not specified [RCV004321463]	uncertain significance	7	130276661	130276661	Human		name
401898220	CV2790964	single nucleotide variant	NM_001869.3(CPA2):c.542G>A (p.Arg181Gln)	not specified [RCV004354591]	uncertain significance	7	130275204	130275204	Human		name
405685845	CV3235795	single nucleotide variant	NM_001869.3(CPA2):c.656C>T (p.Pro219Leu)	not specified [RCV004372309]	uncertain significance	7	130276698	130276698	Human		name
405685850	CV3235796	single nucleotide variant	NM_001869.3(CPA2):c.748G>A (p.Gly250Ser)	not specified [RCV004372310]	uncertain significance	7	130277877	130277877	Human		name
405685856	CV3235797	single nucleotide variant	NM_001869.3(CPA2):c.865A>G (p.Ile289Val)	not specified [RCV004372311]	uncertain significance	7	130279540	130279540	Human		name
407457240	CV3419545	single nucleotide variant	NM_001869.3(CPA2):c.631G>T (p.Asp211Tyr)	not specified [RCV004610939]	uncertain significance	7	130276673	130276673	Human		name
407457238	CV3419546	single nucleotide variant	NM_001869.3(CPA2):c.346G>A (p.Gly116Ser)	not specified [RCV004610940]	uncertain significance	7	130270750	130270750	Human		name
597650087	CV3650913	single nucleotide variant	NM_001869.3(CPA2):c.957A>C (p.Lys319Asn)	not specified [RCV004910421]	uncertain significance	7	130279632	130279632	Human		name
597650105	CV3650915	single nucleotide variant	NM_001869.3(CPA2):c.658G>A (p.Val220Ile)	not specified [RCV004910423]	uncertain significance	7	130276700	130276700	Human		name
597650116	CV3650916	single nucleotide variant	NM_001869.3(CPA2):c.482T>C (p.Leu161Pro)	not specified [RCV004910424]	uncertain significance	7	130273173	130273173	Human		name
598235147	CV3945133	single nucleotide variant	NM_001869.3(CPA2):c.326A>G (p.Asn109Ser)	not specified [RCV005320200]	uncertain significance	7	130270730	130270730	Human		name
15184653	CV710769	single nucleotide variant	NM_001869.3(CPA2):c.514A>G (p.Ile172Val)	not provided [RCV000975166]	benign	7	130275176	130275176	Human		name
156372640	CV2194499	single nucleotide variant	NM_001869.3(CPA2):c.1031A>C (p.His344Pro)	not specified [RCV004081570]	uncertain significance	7	130282147	130282147	Human		name
156026733	CV2199169	single nucleotide variant	NM_001869.3(CPA2):c.1033G>A (p.Gly345Ser)	not specified [RCV004080559]	uncertain significance	7	130282149	130282149	Human		name
156203799	CV2256329	single nucleotide variant	NM_001869.3(CPA2):c.1228A>G (p.Ile410Val)	not specified [RCV004116563]	uncertain significance	7	130289715	130289715	Human		name
156057334	CV2375855	single nucleotide variant	NM_001869.3(CPA2):c.1244G>A (p.Arg415Gln)	not specified [RCV004217704]	uncertain significance	7	130289731	130289731	Human		name
401733836	CV2687362	single nucleotide variant	NM_001869.3(CPA2):c.1214T>C (p.Leu405Pro)	not specified [RCV004298290]	uncertain significance	7	130289701	130289701	Human		name
401893286	CV2766403	single nucleotide variant	NM_001869.3(CPA2):c.1006G>C (p.Ala336Pro)	not specified [RCV004342644]	uncertain significance	7	130282122	130282122	Human		name
405685829	CV3235792	single nucleotide variant	NM_001869.3(CPA2):c.1233G>A (p.Met411Ile)	not specified [RCV004372306]	uncertain significance	7	130289720	130289720	Human		name
405685834	CV3235793	single nucleotide variant	NM_001869.3(CPA2):c.1256A>G (p.Tyr419Cys)	not specified [RCV004372307]	uncertain significance	7	130289743	130289743	Human		name
597650078	CV3650912	single nucleotide variant	NM_001869.3(CPA2):c.1129T>C (p.Phe377Leu)	not specified [RCV004910420]	uncertain significance	7	130289616	130289616	Human		name
598235153	CV3945134	single nucleotide variant	NM_001869.3(CPA2):c.1236G>C (p.Glu412Asp)	not specified [RCV005320201]	uncertain significance	7	130289723	130289723	Human		name

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