"Invitae"[submitter] AND "IGSF10"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2197454	NM_178822.5(IGSF10):c.7854G>A (p.Thr2618=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 708312	NM_178822.5(IGSF10):c.7840G>A (p.Asp2614Asn)	IGSF10, MED12L (D2614N +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1614226	NM_178822.5(IGSF10):c.7735C>T (p.His2579Tyr)	IGSF10 (H2579Y +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2722741	NM_178822.5(IGSF10):c.7730G>C (p.Arg2577Thr)	IGSF10 (R2577T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2723907	NM_178822.5(IGSF10):c.7726G>C (p.Glu2576Gln)	IGSF10 (E555Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1394395	NM_178822.5(IGSF10):c.7715C>T (p.Thr2572Met)	IGSF10 (T2572M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1598558	NM_178822.5(IGSF10):c.7683A>G (p.Thr2561=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1909888	NM_178822.5(IGSF10):c.7586G>A (p.Arg2529Gln)	IGSF10 (R2529Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1441895	NM_178822.5(IGSF10):c.7567_7570dup (p.Val2524fs)	IGSF10 (V503fs +1 more)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 732950	NM_178822.5(IGSF10):c.7568T>C (p.Ile2523Thr)	IGSF10 (I2523T +1 more)	Single nucleotide variant (missense variant)	IGSF10-related condition +1 more	GBenign
Select item 2751965	NM_178822.5(IGSF10):c.7565T>A (p.Met2522Lys)	IGSF10 (M501K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2720758	NM_178822.5(IGSF10):c.7548_7551dup (p.Thr2518fs)	IGSF10 (T497fs +1 more)	Duplication (frameshift variant)	not provided +1 more	GBenign
Select item 1532394	NM_178822.5(IGSF10):c.7539T>C (p.Gly2513=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1946452	NM_178822.5(IGSF10):c.7429C>T (p.Pro2477Ser)	IGSF10 (P456S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1663673	NM_178822.5(IGSF10):c.7426A>T (p.Arg2476Trp)	IGSF10 (R2476W +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 784027	NM_178822.5(IGSF10):c.7374A>G (p.Gly2458=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 712512	NM_178822.5(IGSF10):c.7350_7353dup (p.Leu2452fs)	IGSF10 (L2452fs +1 more)	Duplication (frameshift variant)	not provided	GLikely benign
Select item 775917	NM_178822.5(IGSF10):c.7348C>T (p.Leu2450=)	IGSF10	Single nucleotide variant (synonymous variant)	IGSF10-related condition +1 more	GBenign/Likely benign
Select item 2018616	NM_178822.5(IGSF10):c.7342G>T (p.Glu2448Ter)	IGSF10 (E427* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2045068	NM_178822.5(IGSF10):c.7334_7336dup (p.Ile2445_Ser2446insIle)	IGSF10	Duplication (inframe_insertion)	not provided	GUncertain significance
Select item 3002249	NM_178822.5(IGSF10):c.7314A>G (p.Ala2438=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2070440	NM_178822.5(IGSF10):c.7311T>C (p.Tyr2437=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 787612	NM_178822.5(IGSF10):c.7305T>C (p.Leu2435=)	IGSF10	Single nucleotide variant (synonymous variant)	IGSF10-related condition +1 more	GBenign/Likely benign
Select item 2458905	NM_178822.5(IGSF10):c.7273A>C (p.Ile2425Leu)	IGSF10 (I2425L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 787613	NM_178822.5(IGSF10):c.7254C>T (p.Gly2418=)	IGSF10	Single nucleotide variant (synonymous variant)	IGSF10-related condition +1 more	GBenign/Likely benign
Select item 2181900	NM_178822.5(IGSF10):c.7229G>A (p.Arg2410His)	IGSF10 (R389H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 756898	NM_178822.5(IGSF10):c.7217C>T (p.Ala2406Val)	IGSF10 (A2406V +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2981566	NM_178822.5(IGSF10):c.7152_7153del (p.Ser2385fs)	IGSF10 (S364fs +1 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 767939	NM_178822.5(IGSF10):c.7152A>G (p.Gln2384=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1936149	NM_178822.5(IGSF10):c.7151A>G (p.Gln2384Arg)	IGSF10 (Q2384R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2895264	NM_178822.5(IGSF10):c.7109T>C (p.Ile2370Thr)	IGSF10 (I349T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1601101	NM_178822.5(IGSF10):c.7101T>G (p.Pro2367=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2421603	NM_178822.5(IGSF10):c.7096C>T (p.Pro2366Ser)	IGSF10 (P2366S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2051037	NM_178822.5(IGSF10):c.7080T>C (p.Ser2360=)	IGSF10	Single nucleotide variant (synonymous variant)	IGSF10-related condition +1 more	GLikely benign
Select item 1476462	NM_178822.5(IGSF10):c.7079C>T (p.Ser2360Phe)	IGSF10 (S2360F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2715053	NM_178822.5(IGSF10):c.7010C>T (p.Pro2337Leu)	IGSF10 (P316L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1355362	NM_178822.5(IGSF10):c.6977T>C (p.Val2326Ala)	IGSF10 (V2326A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2419163	NM_178822.5(IGSF10):c.6967G>A (p.Val2323Met)	IGSF10 (V2323M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1640207	NM_178822.5(IGSF10):c.6966C>T (p.Ser2322=)	IGSF10	Single nucleotide variant (synonymous variant)	IGSF10-related condition +1 more	GBenign
Select item 2048358	NM_178822.5(IGSF10):c.6927C>T (p.Ala2309=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2038330	NM_178822.5(IGSF10):c.6908_6909del (p.Val2303fs)	IGSF10 (V2303fs +1 more)	Microsatellite (frameshift variant)	not provided	GUncertain significance
Select item 1924918	NM_178822.5(IGSF10):c.6772C>T (p.His2258Tyr)	IGSF10 (H2258Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1600158	NM_178822.5(IGSF10):c.6729C>T (p.Asn2243=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2794345	NM_178822.5(IGSF10):c.6692T>G (p.Val2231Gly)	IGSF10 (V210G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1940659	NM_178822.5(IGSF10):c.6686A>C (p.Asp2229Ala)	IGSF10 (D2229A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1633498	NM_178822.5(IGSF10):c.6647G>A (p.Arg2216Gln)	IGSF10 (R195Q +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1406850	NM_178822.5(IGSF10):c.6634_6635del (p.Val2212fs)	IGSF10 (V2212fs +1 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2722581	NM_178822.5(IGSF10):c.6633C>T (p.Tyr2211=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1599482	NM_178822.5(IGSF10):c.6591T>G (p.Ser2197=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1511829	NM_178822.5(IGSF10):c.6581C>T (p.Ala2194Val)	IGSF10 (A173V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 773140	NM_178822.5(IGSF10):c.6483T>C (p.Leu2161=)	IGSF10	Single nucleotide variant (synonymous variant)	IGSF10-related condition +1 more	GBenign
Select item 732951	NM_178822.5(IGSF10):c.6447C>T (p.Thr2149=)	IGSF10	Single nucleotide variant (synonymous variant)	IGSF10-related condition +1 more	GBenign
Select item 2144519	NM_178822.5(IGSF10):c.6431G>A (p.Arg2144Lys)	IGSF10 (R123K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 791957	NM_178822.5(IGSF10):c.6336G>A (p.Ala2112=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 746778	NM_178822.5(IGSF10):c.6336G>T (p.Ala2112=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2859841	NM_178822.5(IGSF10):c.6302A>T (p.Asn2101Ile)	IGSF10 (N2101I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2728822	NM_178822.5(IGSF10):c.6231A>C (p.Gly2077=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 769615	NM_178822.5(IGSF10):c.6189C>T (p.Ser2063=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2064207	NM_178822.5(IGSF10):c.6006T>G (p.Phe2002Leu)	IGSF10 (F2002L)	Single nucleotide variant (5 prime UTR variant +1 more)	IGSF10-related condition +1 more	GConflicting classifications of pathogenicity
Select item 2917716	NM_178822.5(IGSF10):c.5996dup (p.Ser2000fs)	IGSF10 (S2000fs)	Duplication (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 2722210	NM_178822.5(IGSF10):c.5990C>T (p.Pro1997Leu)	IGSF10 (P1997L)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 1500871	NM_178822.5(IGSF10):c.5988C>A (p.Tyr1996Ter)	IGSF10 (Y1996*)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 2706771	NM_178822.5(IGSF10):c.5983G>A (p.Val1995Ile)	IGSF10 (V1995I)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1617591	NM_178822.5(IGSF10):c.5973C>T (p.Ser1991=)	IGSF10	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign
Select item 1988108	NM_178822.5(IGSF10):c.5964-17dup	IGSF10	Duplication (intron variant)	not provided	GBenign
Select item 2747034	NM_178822.5(IGSF10):c.5939A>G (p.Lys1980Arg)	IGSF10 (K1980R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1487142	NM_178822.5(IGSF10):c.5921T>C (p.Met1974Thr)	IGSF10 (M1974T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2513166	NM_178822.5(IGSF10):c.5860A>T (p.Asn1954Tyr)	IGSF10 (N1954Y)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1391066	NM_178822.5(IGSF10):c.5837C>T (p.Ala1946Val)	IGSF10 (A1946V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2809438	NM_178822.5(IGSF10):c.5820C>A (p.Ser1940Arg)	IGSF10 (S1940R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1616665	NM_178822.5(IGSF10):c.5799A>G (p.Thr1933=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3012107	NM_178822.5(IGSF10):c.5775G>A (p.Ser1925=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2067251	NM_178822.5(IGSF10):c.5718C>T (p.Asn1906=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1384213	NM_178822.5(IGSF10):c.5696A>G (p.Asn1899Ser)	IGSF10 (N1899S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2188858	NM_178822.5(IGSF10):c.5635T>G (p.Ser1879Ala)	IGSF10 (S1879A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1546554	NM_178822.5(IGSF10):c.5623T>C (p.Tyr1875His)	IGSF10 (Y1875H)	Single nucleotide variant (missense variant)	IGSF10-related condition +1 more	GBenign
Select item 2815259	NM_178822.5(IGSF10):c.5511C>A (p.Val1837=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 812134	NM_178822.5(IGSF10):c.5477G>A (p.Gly1826Asp)	IGSF10 (G1826D)	Single nucleotide variant (missense variant)	Premature ovarian failure +1 more	GUncertain significance
Select item 788851	NM_178822.5(IGSF10):c.5405A>T (p.Asp1802Val)	IGSF10 (D1802V)	Single nucleotide variant (missense variant)	IGSF10-related condition +1 more	GBenign/Likely benign
Select item 1608084	NM_178822.5(IGSF10):c.5363C>G (p.Ser1788Ter)	IGSF10 (S1788*)	Single nucleotide variant (nonsense)	not provided	GLikely benign
Select item 769616	NM_178822.5(IGSF10):c.5307A>G (p.Ala1769=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 2072802	NM_178822.5(IGSF10):c.5278G>T (p.Gly1760Ter)	IGSF10 (G1760*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2890683	NM_178822.5(IGSF10):c.5277C>T (p.Ser1759=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2882257	NM_178822.5(IGSF10):c.5173G>A (p.Ala1725Thr)	IGSF10 (A1725T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1532253	NM_178822.5(IGSF10):c.5063-8C>A	IGSF10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1902380	NM_178822.5(IGSF10):c.5062+20T>A	IGSF10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2073000	NM_178822.5(IGSF10):c.5062+5G>A	IGSF10	Single nucleotide variant (intron variant)	IGSF10-related condition +1 more	GBenign
Select item 2195763	NM_178822.5(IGSF10):c.5051G>C (p.Arg1684Thr)	IGSF10 (R1684T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2873524	NM_178822.5(IGSF10):c.5033C>T (p.Pro1678Leu)	IGSF10 (P1678L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2123545	NM_178822.5(IGSF10):c.5012A>C (p.Glu1671Ala)	IGSF10 (E1671A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2419892	NM_178822.5(IGSF10):c.4906C>T (p.Pro1636Ser)	IGSF10 (P1636S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 727766	NM_178822.5(IGSF10):c.4804G>T (p.Glu1602Ter)	IGSF10 (E1602*)	Single nucleotide variant (nonsense)	not provided	GLikely benign
Select item 1421535	NM_178822.5(IGSF10):c.4748T>C (p.Ile1583Thr)	IGSF10 (I1583T)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 2074505	NM_178822.5(IGSF10):c.4737A>T (p.Pro1579=)	IGSF10	Single nucleotide variant (synonymous variant)	IGSF10-related condition +1 more	GLikely benign
Select item 710624	NM_178822.5(IGSF10):c.4636C>T (p.Leu1546=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1553357	NM_178822.5(IGSF10):c.4607T>C (p.Ile1536Thr)	IGSF10 (I1536T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 718428	NM_178822.5(IGSF10):c.4596C>T (p.Ala1532=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1967577	NM_178822.5(IGSF10):c.4576C>T (p.Pro1526Ser)	IGSF10 (P1526S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2886604	NM_178822.5(IGSF10):c.4575C>T (p.Ser1525=)	IGSF10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 789719	NM_178822.5(IGSF10):c.4564G>A (p.Val1522Ile)	IGSF10 (V1522I)	Single nucleotide variant (missense variant)	IGSF10-related condition +1 more	GBenign

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