"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "ATP2B4" - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1626186	NM_001684.5(ATP2B4):c.5C>T (p.Thr2Met)	ATP2B4 (T2M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 705092	NM_001684.5(ATP2B4):c.19C>A (p.Arg7Ser)	ATP2B4 (R7S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 703903	NM_001684.5(ATP2B4):c.19C>T (p.Arg7Cys)	ATP2B4 (R7C)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1505093	NM_001684.5(ATP2B4):c.20G>A (p.Arg7His)	ATP2B4 (R7H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1643189	NM_001684.5(ATP2B4):c.39G>A (p.Ser13=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1631913	NM_001684.5(ATP2B4):c.41T>C (p.Met14Thr)	ATP2B4 (M14T)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2986609	NM_001684.5(ATP2B4):c.53G>A (p.Arg18His)	ATP2B4 (R18H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1598820	NM_001684.5(ATP2B4):c.111A>G (p.Ser37=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1584699	NM_001684.5(ATP2B4):c.136G>A (p.Val46Ile)	ATP2B4 (V46I)	Single nucleotide variant (missense variant)	not provided	GBenign/Likely benign
Select item 2042901	NM_001684.5(ATP2B4):c.162C>T (p.Leu54=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2009191	NM_001684.5(ATP2B4):c.179C>T (p.Thr60Ile)	ATP2B4 (T60I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1600570	NM_001684.5(ATP2B4):c.318T>C (p.Leu106=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2989802	NM_001684.5(ATP2B4):c.342C>T (p.Ile114=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1369577	NM_001684.5(ATP2B4):c.368G>A (p.Arg123His)	ATP2B4 (R123H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1393853	NM_001684.5(ATP2B4):c.415C>T (p.Pro139Ser)	ATP2B4 (P139S)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 734727	NM_001684.5(ATP2B4):c.423T>C (p.Asp141=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1948379	NM_001684.5(ATP2B4):c.547C>T (p.Arg183Cys)	ATP2B4 (R183C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2719758	NM_001684.5(ATP2B4):c.552T>G (p.Ile184Met)	ATP2B4 (I184M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2976092	NM_001684.5(ATP2B4):c.561G>A (p.Glu187=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2420810	NM_001684.5(ATP2B4):c.585C>T (p.Asn195=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1936256	NM_001684.5(ATP2B4):c.650-6C>T	ATP2B4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1626597	NM_001684.5(ATP2B4):c.687G>A (p.Gly229=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2693838	NM_001684.5(ATP2B4):c.753C>G (p.Asp251Glu)	ATP2B4 (D251E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1605037	NM_001684.5(ATP2B4):c.775+9C>G	ATP2B4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1715445	NM_001684.5(ATP2B4):c.832T>G (p.Ser278Ala)	ATP2B4 (S278A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1967701	NM_001684.5(ATP2B4):c.863G>A (p.Gly288Glu)	ATP2B4 (G288E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 705093	NM_001684.5(ATP2B4):c.863G>T (p.Gly288Val)	ATP2B4 (G288V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2764324	NM_001684.5(ATP2B4):c.938-3C>T	ATP2B4	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1914296	NM_001684.5(ATP2B4):c.951C>T (p.Asp317=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2066524	NM_001684.5(ATP2B4):c.996C>T (p.Ile332=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 703837	NM_001684.5(ATP2B4):c.1025T>C (p.Val342Ala)	ATP2B4 (V342A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1663819	NM_001684.5(ATP2B4):c.1059G>A (p.Gln353=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1901339	NM_001684.5(ATP2B4):c.1092G>A (p.Gly364=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1598801	NM_001684.5(ATP2B4):c.1122G>A (p.Thr374=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1956870	NM_001684.5(ATP2B4):c.1151T>C (p.Ile384Thr)	ATP2B4 (I384T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2697052	NM_001684.5(ATP2B4):c.1269G>A (p.Glu423=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1400320	NM_001684.5(ATP2B4):c.1421G>A (p.Arg474His)	ATP2B4 (R474H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1989519	NM_001684.5(ATP2B4):c.1463G>A (p.Arg488His)	ATP2B4 (R488H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2727165	NM_001684.5(ATP2B4):c.1500C>T (p.Val500=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2406792	NM_001684.5(ATP2B4):c.1504G>A (p.Asp502Asn)	ATP2B4 (D502N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 703944	NM_001684.5(ATP2B4):c.1545C>T (p.Thr515=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1578067	NM_001684.5(ATP2B4):c.1557+18G>A	ATP2B4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2973914	NM_001684.5(ATP2B4):c.1558C>G (p.Pro520Ala)	ATP2B4 (P520A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2196622	NM_001684.5(ATP2B4):c.1585C>T (p.Arg529Trp)	ATP2B4 (R529W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1606963	NM_001684.5(ATP2B4):c.1605C>T (p.Thr535=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1507243	NM_001684.5(ATP2B4):c.1606G>A (p.Glu536Lys)	ATP2B4 (E536K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1512221	NM_001684.5(ATP2B4):c.1627G>A (p.Val543Ile)	ATP2B4 (V543I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2201123	NM_001684.5(ATP2B4):c.1656T>A (p.Ala552=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2324066	NM_001684.5(ATP2B4):c.1660C>T (p.Arg554Cys)	ATP2B4 (R554C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 703855	NM_001684.5(ATP2B4):c.1665T>C (p.Asn555=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2639819	NM_001684.5(ATP2B4):c.1674C>T (p.Pro558=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2782500	NM_001684.5(ATP2B4):c.1688A>G (p.Tyr563Cys)	ATP2B4 (Y563C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2058863	NM_001684.5(ATP2B4):c.1748A>G (p.Asn583Ser)	ATP2B4 (N583S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2986858	NM_001684.5(ATP2B4):c.1776C>T (p.Gly592=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2956886	NM_001684.5(ATP2B4):c.1799+12C>T	ATP2B4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1631168	NM_001684.5(ATP2B4):c.1799+17A>G	ATP2B4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1151049	NM_001684.5(ATP2B4):c.1826G>C (p.Gly609Ala)	ATP2B4 (G609A)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 704204	NM_001684.5(ATP2B4):c.1839A>T (p.Pro613=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1601706	NM_001684.5(ATP2B4):c.1846A>C (p.Asn616His)	ATP2B4 (N616H)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2889882	NM_001684.5(ATP2B4):c.1900G>A (p.Gly634Arg)	ATP2B4 (G634R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1605038	NM_001684.5(ATP2B4):c.1902A>C (p.Gly634=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2058129	NM_001684.5(ATP2B4):c.1918A>G (p.Ile640Val)	ATP2B4 (I640V)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 2420905	NM_001684.5(ATP2B4):c.1936G>A (p.Asp646Asn)	ATP2B4 (D646N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 703856	NM_001684.5(ATP2B4):c.1968T>C (p.Asn656=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2993409	NM_001684.5(ATP2B4):c.1974C>A (p.Ile658=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 706579	NM_001684.5(ATP2B4):c.1981G>A (p.Glu661Lys)	ATP2B4 (E661K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2954888	NM_001684.5(ATP2B4):c.1995C>T (p.Ile665=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1592848	NM_001684.5(ATP2B4):c.1996G>A (p.Ala666Thr)	ATP2B4 (A666T)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 2802653	NM_001684.5(ATP2B4):c.1998G>A (p.Ala666=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1589766	NM_001684.5(ATP2B4):c.2032-3T>C	ATP2B4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1944797	NM_001684.5(ATP2B4):c.2052A>G (p.Lys684=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2850968	NM_001684.5(ATP2B4):c.2110C>T (p.Arg704Trp)	ATP2B4 (R704W)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3020971	NM_001684.5(ATP2B4):c.2116A>G (p.Ile706Val)	ATP2B4 (I706V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2111146	NM_001684.5(ATP2B4):c.2160G>A (p.Leu720=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2977861	NM_001684.5(ATP2B4):c.2194C>T (p.Arg732Cys)	ATP2B4 (R732C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2085060	NM_001684.5(ATP2B4):c.2195G>A (p.Arg732His)	ATP2B4 (R732H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1584107	NM_001684.5(ATP2B4):c.2199C>T (p.Asn733=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1630135	NM_001684.5(ATP2B4):c.2211+17G>A	ATP2B4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2867944	NM_001684.5(ATP2B4):c.2264G>T (p.Arg755Leu)	ATP2B4 (R755L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1545997	NM_001684.5(ATP2B4):c.2271T>A (p.Ser757=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2971708	NM_001684.5(ATP2B4):c.2289C>T (p.Thr763=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1656946	NM_001684.5(ATP2B4):c.2300-13C>T	ATP2B4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1606816	NM_001684.5(ATP2B4):c.2300-11G>A	ATP2B4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1939014	NM_001684.5(ATP2B4):c.2392G>A (p.Val798Ile)	ATP2B4 (V798I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2991589	NM_001684.5(ATP2B4):c.2492T>C (p.Met831Thr)	ATP2B4 (M831T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2054753	NM_001684.5(ATP2B4):c.2562C>T (p.Ala854=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2090759	NM_001684.5(ATP2B4):c.2591T>A (p.Ile864Asn)	ATP2B4 (I864N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1912401	NM_001684.5(ATP2B4):c.2599-6C>T	ATP2B4	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1667210	NM_001684.5(ATP2B4):c.2680C>T (p.Pro894Ser)	ATP2B4 (P894S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2852630	NM_001684.5(ATP2B4):c.2682C>G (p.Pro894=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2421365	NM_001684.5(ATP2B4):c.2707C>T (p.Arg903Cys)	ATP2B4 (R903C)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2421478	NM_001684.5(ATP2B4):c.2712C>T (p.Pro904=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2852375	NM_001684.5(ATP2B4):c.2730T>G (p.Pro910=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2863536	NM_001684.5(ATP2B4):c.2775C>G (p.Phe925Leu)	ATP2B4 (F925L)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1580594	NM_001684.5(ATP2B4):c.2811G>A (p.Ala937=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 706059	NM_001684.5(ATP2B4):c.2819A>G (p.Lys940Arg)	ATP2B4 (K940R)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 2728452	NM_001684.5(ATP2B4):c.2824T>C (p.Phe942Leu)	ATP2B4 (F942L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1386404	NM_001684.5(ATP2B4):c.2952G>C (p.Glu984Asp)	ATP2B4 (E984D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2050073	NM_001684.5(ATP2B4):c.2959G>A (p.Val987Ile)	ATP2B4 (V987I)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1631712	NM_001684.5(ATP2B4):c.2973C>T (p.Ile991=)	ATP2B4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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