Related gene-specific medical variations for Gene (Select 100526693) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3463651	NM_001387446.1(TTLL3):c.1712G>T (p.Gly571Val)	ARPC4-TTLL3, TTLL3 (G495V +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3463649	NM_001387446.1(TTLL3):c.1741A>G (p.Ile581Val)	ARPC4-TTLL3, TTLL3 (I525V +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3463648	NM_001387446.1(TTLL3):c.2115G>C (p.Leu705Phe)	ARPC4-TTLL3, TTLL3 (L506F +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3463647	NM_001387446.1(TTLL3):c.-80C>G	ARPC4-TTLL3, LOC129936138 +1 more (P117R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3463646	NM_001387446.1(TTLL3):c.2102G>C (p.Cys701Ser)	ARPC4-TTLL3, TTLL3 (C502S +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3463645	NM_001025930.5(TTLL3):c.110T>C (p.Leu37Pro)	ARPC4-TTLL3, LOC129936138 +1 more (L37P)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3463644	NM_001387446.1(TTLL3):c.1715T>C (p.Ile572Thr)	ARPC4-TTLL3, TTLL3 (I572T +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3463643	NM_001387446.1(TTLL3):c.-170C>G	ARPC4-TTLL3, LOC129936138 +1 more (P87R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3463642	NM_001387446.1(TTLL3):c.2132T>C (p.Leu711Pro)	ARPC4-TTLL3, TTLL3 (L711P +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3463641	NM_001387446.1(TTLL3):c.563A>T (p.Asp188Val)	ARPC4-TTLL3, TTLL3 (D188V +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3431771	NM_001198793.1(ARPC4-TTLL3):c.75C>G (p.Phe25Leu)	ARPC4, ARPC4-TTLL3 (F25L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3431768	NM_005718.5(ARPC4):c.3+11C>G	ARPC4, ARPC4-TTLL3 (P5R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3366016	NM_005718.5(ARPC4):c.475A>G (p.Ile159Val)	ARPC4, ARPC4-TTLL3 (I159V +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3338496	NM_005718.5(ARPC4):c.3+14G>C	ARPC4, ARPC4-TTLL3 (G6A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3330000	NM_001025930.5(TTLL3):c.137G>A (p.Arg46His)	ARPC4-TTLL3, LOC129936138 +1 more (R46H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3329999	NM_001387446.1(TTLL3):c.-105G>A	ARPC4-TTLL3, LOC129936138 +1 more (A109T)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3329998	NM_001387446.1(TTLL3):c.584G>A (p.Arg195His)	ARPC4-TTLL3, TTLL3 (R151H +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3329997	NM_001387446.1(TTLL3):c.2176G>C (p.Asp726His)	ARPC4-TTLL3, TTLL3 (D527H +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3329996	NM_001025930.5(TTLL3):c.173G>T (p.Arg58Leu)	ARPC4-TTLL3, LOC129936138 +1 more (R58L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3329995	NM_001387446.1(TTLL3):c.583C>T (p.Arg195Cys)	ARPC4-TTLL3, TTLL3 (R152C +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3315969	NM_005718.5(ARPC4):c.3+11C>T	ARPC4, ARPC4-TTLL3 (P5L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3184596	NM_001387446.1(TTLL3):c.40G>A (p.Ala14Thr)	ARPC4-TTLL3, TTLL3 (A62T +2 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3184595	NM_001387446.1(TTLL3):c.-84G>A	ARPC4-TTLL3, LOC129936138 +1 more (G116S)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3184594	NM_001387446.1(TTLL3):c.-89C>T	ARPC4-TTLL3, LOC129936138 +1 more (P114L)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3184593	NM_001387446.1(TTLL3):c.2264G>A (p.Arg755His)	ARPC4-TTLL3, TTLL3 (R556H +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GLikely benign
Select item 3184592	NM_001025930.5(TTLL3):c.239G>T (p.Gly80Val)	ARPC4-TTLL3, LOC129936138 +1 more (G80V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3184591	NM_001387446.1(TTLL3):c.1772G>A (p.Arg591Gln)	ARPC4-TTLL3, TTLL3 (R336Q +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3184590	NM_001387446.1(TTLL3):c.1717C>T (p.Arg573Trp)	ARPC4-TTLL3, TTLL3 (R318W +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3184589	NM_001025930.5(TTLL3):c.185G>A (p.Arg62Lys)	ARPC4-TTLL3, LOC129936138 +1 more (R62K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3184587	NM_001025930.5(TTLL3):c.104A>C (p.Asn35Thr)	ARPC4-TTLL3, LOC129936138 +1 more (N35T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129801	NM_001198793.1(ARPC4-TTLL3):c.899A>G (p.Gln300Arg)	ARPC4-TTLL3, TTLL3 (Q238R +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129800	NM_001198793.1(ARPC4-TTLL3):c.845C>T (p.Ala282Val)	ARPC4-TTLL3, TTLL3 (A220V +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129799	NM_001198793.1(ARPC4-TTLL3):c.829G>A (p.Asp277Asn)	ARPC4-TTLL3, TTLL3 (D183N +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129798	NM_001198793.1(ARPC4-TTLL3):c.814G>C (p.Ala272Pro)	ARPC4-TTLL3, TTLL3 (A211P +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129797	NM_001198793.1(ARPC4-TTLL3):c.629C>T (p.Pro210Leu)	ARPC4-TTLL3, TTLL3 (P210L +5 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3129796	NM_001198793.1(ARPC4-TTLL3):c.584C>T (p.Thr195Ile)	ARPC4-TTLL3, TTLL3 (T149I +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129795	NM_001198793.1(ARPC4-TTLL3):c.580G>A (p.Gly194Arg)	ARPC4-TTLL3, TTLL3 (G148R +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129794	NM_001198793.1(ARPC4-TTLL3):c.519G>C (p.Glu173Asp)	ARPC4-TTLL3, TTLL3 (E173D +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129793	NM_001198793.1(ARPC4-TTLL3):c.482G>A (p.Ser161Asn)	ARPC4-TTLL3, TTLL3 (S66N +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129792	NM_001198793.1(ARPC4-TTLL3):c.479A>G (p.Asp160Gly)	ARPC4-TTLL3, TTLL3 (D114G +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129791	NM_001198793.1(ARPC4-TTLL3):c.386G>A (p.Arg129His)	ARPC4-TTLL3, TTLL3 (R35H +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129790	NM_001198793.1(ARPC4-TTLL3):c.373C>T (p.Arg125Trp)	ARPC4-TTLL3, TTLL3 (R125W +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129789	NM_001198793.1(ARPC4-TTLL3):c.371T>C (p.Ile124Thr)	ARPC4-TTLL3, TTLL3 (I124T +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129788	NM_001198793.1(ARPC4-TTLL3):c.1726A>G (p.Ile576Val)	ARPC4-TTLL3, TTLL3 (I514V +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129787	NM_001198793.1(ARPC4-TTLL3):c.1712G>C (p.Gly571Ala)	ARPC4-TTLL3, TTLL3 (G298A +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129786	NM_001198793.1(ARPC4-TTLL3):c.1697G>C (p.Arg566Pro)	ARPC4-TTLL3, TTLL3 (R505P +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129785	NM_001198793.1(ARPC4-TTLL3):c.1697G>A (p.Arg566His)	ARPC4-TTLL3, TTLL3 (R293H +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129784	NM_001198793.1(ARPC4-TTLL3):c.1696C>T (p.Arg566Cys)	ARPC4-TTLL3, TTLL3 (R384C +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129783	NM_001198793.1(ARPC4-TTLL3):c.1669C>T (p.Arg557Cys)	ARPC4-TTLL3, TTLL3 (R284C +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129782	NM_001198793.1(ARPC4-TTLL3):c.1651G>A (p.Val551Met)	ARPC4-TTLL3, TTLL3 (V369M +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129780	NM_001198793.1(ARPC4-TTLL3):c.1649G>C (p.Gly550Ala)	ARPC4-TTLL3, TTLL3 (G277A +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129779	NM_001198793.1(ARPC4-TTLL3):c.1631C>A (p.Thr544Asn)	ARPC4-TTLL3, TTLL3 (T271N +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129778	NM_001198793.1(ARPC4-TTLL3):c.1602C>A (p.Ser534Arg)	ARPC4-TTLL3, TTLL3 (S472R +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129777	NM_001198793.1(ARPC4-TTLL3):c.1597G>A (p.Ala533Thr)	ARPC4-TTLL3, TTLL3 (A459T +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129776	NM_001198793.1(ARPC4-TTLL3):c.1555G>A (p.Val519Met)	ARPC4-TTLL3, TTLL3 (V412M +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129775	NM_001198793.1(ARPC4-TTLL3):c.1445C>A (p.Ser482Tyr)	ARPC4-TTLL3, TTLL3 (S300Y +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129774	NM_001198793.1(ARPC4-TTLL3):c.1385T>C (p.Met462Thr)	ARPC4-TTLL3, TTLL3 (M368T +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129773	NM_001198793.1(ARPC4-TTLL3):c.1363C>T (p.Pro455Ser)	ARPC4-TTLL3, TTLL3 (P361S +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129772	NM_001198793.1(ARPC4-TTLL3):c.1358G>A (p.Arg453Gln)	ARPC4-TTLL3, TTLL3 (R180Q +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129770	NM_001198793.1(ARPC4-TTLL3):c.1342G>C (p.Glu448Gln)	ARPC4-TTLL3, TTLL3 (E387Q +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129769	NM_001198793.1(ARPC4-TTLL3):c.1315T>C (p.Cys439Arg)	ARPC4-TTLL3, TTLL3 (C345R +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129768	NM_001198793.1(ARPC4-TTLL3):c.1271C>T (p.Thr424Met)	ARPC4-TTLL3, TTLL3 (T373M +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129767	NM_001198793.1(ARPC4-TTLL3):c.1262G>A (p.Arg421His)	ARPC4-TTLL3, TTLL3 (R359H +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129766	NM_001198793.1(ARPC4-TTLL3):c.1261C>T (p.Arg421Cys)	ARPC4-TTLL3, TTLL3 (R148C +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129765	NM_001198793.1(ARPC4-TTLL3):c.1249G>A (p.Asp417Asn)	ARPC4-TTLL3, TTLL3 (D144N +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129764	NM_001198793.1(ARPC4-TTLL3):c.1247G>A (p.Arg416His)	ARPC4-TTLL3, TTLL3 (R234H +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129763	NM_001198793.1(ARPC4-TTLL3):c.1246C>T (p.Arg416Cys)	ARPC4-TTLL3, TTLL3 (R143C +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129762	NM_001198793.1(ARPC4-TTLL3):c.1225C>G (p.Pro409Ala)	ARPC4-TTLL3, TTLL3 (P136A +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129761	NM_001198793.1(ARPC4-TTLL3):c.1160G>A (p.Arg387Gln)	ARPC4-TTLL3, TTLL3 (R469Q +9 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129760	NM_001198793.1(ARPC4-TTLL3):c.1110C>A (p.Asn370Lys)	ARPC4-TTLL3, TTLL3 (N319K +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129759	NM_001198793.1(ARPC4-TTLL3):c.1088T>C (p.Met363Thr)	ARPC4-TTLL3, TTLL3 (M360T +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129758	NM_001198793.1(ARPC4-TTLL3):c.1066T>C (p.Cys356Arg)	ARPC4-TTLL3, TTLL3 (C295R +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129757	NM_001198793.1(ARPC4-TTLL3):c.1051G>A (p.Gly351Arg)	ARPC4-TTLL3, TTLL3 (G257R +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129756	NM_001198793.1(ARPC4-TTLL3):c.1010A>G (p.Asp337Gly)	ARPC4-TTLL3, TTLL3 (D243G +8 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3129755	NM_005718.5(ARPC4):c.240T>G (p.Asp80Glu)	ARPC4, ARPC4-TTLL3 (D99E +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3129754	NM_005718.5(ARPC4):c.3+16C>T	ARPC4, ARPC4-TTLL3 (P7S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2602155	NM_001198793.1(ARPC4-TTLL3):c.1546G>A (p.Ala516Thr)	ARPC4-TTLL3, TTLL3 (A442T +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2594010	NM_001198793.1(ARPC4-TTLL3):c.1703G>C (p.Cys568Ser)	ARPC4-TTLL3, TTLL3 (C386S +11 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2570101	NM_001387446.1(TTLL3):c.2306G>A (p.Arg769Gln)	ARPC4-TTLL3, TTLL3 (R726Q +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2545856	NM_001387446.1(TTLL3):c.2027C>T (p.Ala676Val)	ARPC4-TTLL3, TTLL3 (A600V +4 more)	Single nucleotide variant (3 prime UTR variant +3 more)	not specified	GUncertain significance
Select item 2543369	NM_001387446.1(TTLL3):c.-20G>A	ARPC4-TTLL3, TTLL3 (G137E +1 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2524270	NM_001387446.1(TTLL3):c.2311C>T (p.Pro771Ser)	ARPC4-TTLL3, TTLL3 (P572S +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2521832	NM_001025930.5(TTLL3):c.130G>A (p.Glu44Lys)	ARPC4-TTLL3, LOC129936138 +1 more (E44K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2521284	NM_001387446.1(TTLL3):c.-87C>T	ARPC4-TTLL3, LOC129936138 +1 more (L115F)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2473262	NM_001387446.1(TTLL3):c.1828C>T (p.Arg610Cys)	ARPC4-TTLL3, TTLL3 (P586L +7 more)	Single nucleotide variant (synonymous variant +3 more)	not specified	GUncertain significance
Select item 2405090	NM_001387446.1(TTLL3):c.1035G>A (p.Met345Ile)	ARPC4-TTLL3, TTLL3 (M301I +9 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2387631	NM_005718.5(ARPC4):c.3+38G>A	ARPC4, ARPC4-TTLL3 (C14Y)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2371258	NM_001387446.1(TTLL3):c.1784G>A (p.Arg595His)	ARPC4-TTLL3, TTLL3 (R340H +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2361077	NM_001387446.1(TTLL3):c.-134C>T	ARPC4-TTLL3, LOC129936138 +1 more (T99M)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2360177	NM_001387446.1(TTLL3):c.-77C>T	ARPC4-TTLL3, LOC129936138 +1 more (P118L)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2358817	NM_001387446.1(TTLL3):c.2317G>A (p.Ala773Thr)	ARPC4-TTLL3, TTLL3 (A773T +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2354072	NM_001387446.1(TTLL3):c.1906A>G (p.Arg636Gly)	ARPC4-TTLL3, TTLL3 (R677G +7 more)	Single nucleotide variant (synonymous variant +3 more)	not specified	GUncertain significance
Select item 2348825	NM_001387446.1(TTLL3):c.2417C>T (p.Pro806Leu)	ARPC4-TTLL3, TTLL3 (P763L +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2338805	NM_001025930.5(TTLL3):c.71C>A (p.Ser24Tyr)	ARPC4-TTLL3, LOC129936138 +1 more (S24Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2333670	NM_001387446.1(TTLL3):c.-168G>A	ARPC4-TTLL3, LOC129936138 +1 more (A88T)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2330199	NM_001387446.1(TTLL3):c.2069G>C (p.Cys690Ser)	ARPC4-TTLL3, TTLL3 (C491S +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2328648	NM_001387446.1(TTLL3):c.1690G>A (p.Val564Met)	ARPC4-TTLL3, TTLL3 (V531M +6 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2328442	NM_001387446.1(TTLL3):c.2172G>T (p.Arg724Ser)	ARPC4-TTLL3, TTLL3 (R681S +3 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2298497	NM_001198793.1(ARPC4-TTLL3):c.619C>T (p.Arg207Trp)	ARPC4-TTLL3, TTLL3 (R256W +5 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2289437	NM_001198793.1(ARPC4-TTLL3):c.1862C>G (p.Pro621Arg)	ARPC4-TTLL3, TTLL3 (P421R +10 more)	Single nucleotide variant (missense variant +4 more)	not specified	GUncertain significance

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