Anapc7 Variant Search Result - Rat Genome Database

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35 records found for search term Anapc7

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156257616	CV2219907	single nucleotide variant	NM_016238.3(ANAPC7):c.-72T>G	not specified [RCV004095535]	uncertain significance	12	110403699	110403699	Human		name
156276748	CV2351962	single nucleotide variant	NM_016238.3(ANAPC7):c.-57C>G	not specified [RCV004191067]	uncertain significance	12	110403684	110403684	Human		name
405817494	CV3283746	single nucleotide variant	NM_016238.3(ANAPC7):c.-56T>A	not specified [RCV004412404]	uncertain significance	12	110403683	110403683	Human		name
405817484	CV3283756	single nucleotide variant	NM_016238.3(ANAPC7):c.-23T>A	not specified [RCV004412414]	uncertain significance	12	110403650	110403650	Human		name
407474103	CV3453528	single nucleotide variant	NM_016238.3(ANAPC7):c.-57C>T	not specified [RCV004638056]	likely benign	12	110403684	110403684	Human		name
407474266	CV3453553	single nucleotide variant	NM_016238.3(ANAPC7):c.-14C>T	not specified [RCV004638075]	uncertain significance	12	110403641	110403641	Human		name
597632625	CV3698949	single nucleotide variant	NM_016238.3(ANAPC7):c.-72T>A	not specified [RCV004940057]	uncertain significance	12	110403699	110403699	Human		name
151348436	CV1325033	deletion	NM_016238.3(ANAPC7):c.409-2478_818-89del	Ferguson-Bonni neurodevelopmental syndrome [RCV001812627]	pathogenic	12	110383049	110391101	Human	1	name
156099016	CV2367335	single nucleotide variant	NM_016238.3(ANAPC7):c.37G>T (p.Ala13Ser)	not specified [RCV004209243]	uncertain significance	12	110403591	110403591	Human		name
598234489	CV3980075	single nucleotide variant	NM_016238.3(ANAPC7):c.38C>T (p.Ala13Val)	not specified [RCV005363516]	uncertain significance	12	110403590	110403590	Human		name
243051547	CV2415920	single nucleotide variant	NM_016238.3(ANAPC7):c.137T>C (p.Leu46Ser)	Ferguson-Bonni neurodevelopmental syndrome [RCV003148540]	uncertain significance	12	110396417	110396417	Human	1	name
405689985	CV3227321	deletion	NM_016238.3(ANAPC7):c.493del (p.Cys165fs)	Ferguson-Bonni neurodevelopmental syndrome [RCV003991665]	uncertain significance	12	110388539	110388539	Human	1	name
407474222	CV3453538	single nucleotide variant	NM_016238.3(ANAPC7):c.155C>G (p.Ser52Cys)	not specified [RCV004638063]	uncertain significance	12	110396399	110396399	Human		name
407474239	CV3453544	single nucleotide variant	NM_016238.3(ANAPC7):c.292C>A (p.Leu98Ile)	not specified [RCV004638068]	uncertain significance	12	110395217	110395217	Human		name
155915954	CV2200609	single nucleotide variant	NM_016238.3(ANAPC7):c.722G>A (p.Gly241Glu)	not specified [RCV004078948]	uncertain significance	12	110386422	110386422	Human		name
156169008	CV2247286	single nucleotide variant	NM_016238.3(ANAPC7):c.865G>A (p.Asp289Asn)	not specified [RCV004115062]	uncertain significance	12	110382913	110382913	Human		name
401872200	CV2779581	single nucleotide variant	NM_016238.3(ANAPC7):c.830A>G (p.Tyr277Cys)	not specified [RCV004351294]	uncertain significance	12	110382948	110382948	Human		name
405817489	CV3283751	single nucleotide variant	NM_016238.3(ANAPC7):c.454C>A (p.Arg152Ser)	not specified [RCV004412409]	uncertain significance	12	110388578	110388578	Human		name
597795613	CV3698944	single nucleotide variant	NM_016238.3(ANAPC7):c.368C>T (p.Ala123Val)	not specified [RCV004934911]	uncertain significance	12	110395141	110395141	Human		name
597632617	CV3698947	single nucleotide variant	NM_016238.3(ANAPC7):c.799G>C (p.Asp267His)	not specified [RCV004940055]	uncertain significance	12	110386345	110386345	Human		name
597632628	CV3698951	single nucleotide variant	NM_016238.3(ANAPC7):c.864G>C (p.Glu288Asp)	not specified [RCV004940058]	uncertain significance	12	110382914	110382914	Human		name
598234457	CV3980065	single nucleotide variant	NM_016238.3(ANAPC7):c.603G>C (p.Trp201Cys)	not specified [RCV005363512]	uncertain significance	12	110387810	110387810	Human		name
598234591	CV3980109	single nucleotide variant	NM_016238.3(ANAPC7):c.582A>C (p.Gln194His)	not specified [RCV005363531]	uncertain significance	12	110387831	110387831	Human		name
598259355	CV3980119	single nucleotide variant	NM_016238.3(ANAPC7):c.581A>C (p.Gln194Pro)	not specified [RCV005347401]	uncertain significance	12	110387832	110387832	Human		name
598234662	CV3980138	single nucleotide variant	NM_016238.3(ANAPC7):c.756C>G (p.Asp252Glu)	not specified [RCV005363541]	uncertain significance	12	110386388	110386388	Human		name
598234684	CV3980146	single nucleotide variant	NM_016238.3(ANAPC7):c.592A>T (p.Asn198Tyr)	not specified [RCV005363544]	uncertain significance	12	110387821	110387821	Human		name
156233137	CV2273883	single nucleotide variant	NM_016238.3(ANAPC7):c.1087C>T (p.Arg363Trp)	not specified [RCV004132506]	uncertain significance	12	110381797	110381797	Human		name
597632613	CV3698945	single nucleotide variant	NM_016238.3(ANAPC7):c.1402G>A (p.Ala468Thr)	not specified [RCV004940054]	uncertain significance	12	110376172	110376172	Human		name
597795616	CV3698946	single nucleotide variant	NM_016238.3(ANAPC7):c.1525C>G (p.Gln509Glu)	not specified [RCV004934912]	uncertain significance	12	110374317	110374317	Human		name
597632620	CV3698948	single nucleotide variant	NM_016238.3(ANAPC7):c.1192A>G (p.Asn398Asp)	not specified [RCV004940056]	uncertain significance	12	110377558	110377558	Human		name
597632632	CV3698952	single nucleotide variant	NM_016238.3(ANAPC7):c.1621G>A (p.Glu541Lys)	not specified [RCV004940059]	uncertain significance	12	110374221	110374221	Human		name
598259296	CV3980088	single nucleotide variant	NM_016238.3(ANAPC7):c.1459G>A (p.Ala487Thr)	not specified [RCV005347389]	uncertain significance	12	110376115	110376115	Human		name
598212662	CV3980098	single nucleotide variant	NM_016238.3(ANAPC7):c.1219G>A (p.Ala407Thr)	not specified [RCV005358856]	uncertain significance	12	110377531	110377531	Human		name
598234642	CV3980128	single nucleotide variant	NM_016238.3(ANAPC7):c.1005C>G (p.Asn335Lys)	not specified [RCV005363538]	uncertain significance	12	110381879	110381879	Human		name
401932356	CV2816827	microsatellite	NM_016238.3(ANAPC7):c.159_160del (p.Phe54fs)	not provided [RCV003391998]	uncertain significance	12	110396394	110396395	Human		name

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