TRIM10[gene] - ClinVar

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Items: 51

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155430	GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3	ILRUN-AS1, IP6K3 +2582 more	Copy number gain	See cases	GPathogenic
Select item 150044	GRCh38/hg38 6p25.2-21.33(chr6:3224310-30657190)x3	ABCF1, ABT1 +1340 more	Copy number gain	See cases	GPathogenic
Select item 2283019	NM_006778.4(TRIM10):c.1418G>A (p.Arg473Gln)	TRIM10 (R473Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3182209	NM_006778.4(TRIM10):c.1369A>G (p.Thr457Ala)	TRIM10 (T457A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3182208	NM_006778.4(TRIM10):c.1324G>A (p.Val442Met)	TRIM10 (V442M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350263	NM_006778.4(TRIM10):c.1314G>C (p.Glu438Asp)	TRIM10 (E438D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3182207	NM_006778.4(TRIM10):c.1286G>T (p.Arg429Leu)	TRIM10 (R429L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3182206	NM_006778.4(TRIM10):c.1207T>G (p.Trp403Gly)	TRIM10 (W403G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2266770	NM_006778.4(TRIM10):c.1181T>G (p.Leu394Arg)	TRIM10 (L394R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3328622	NM_006778.4(TRIM10):c.1168C>T (p.Arg390Trp)	TRIM10 (R390W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291614	NM_006778.4(TRIM10):c.1147G>C (p.Val383Leu)	TRIM10 (V383L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540930	NM_006778.4(TRIM10):c.1145G>T (p.Gly382Val)	TRIM10 (G382V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3182205	NM_006778.4(TRIM10):c.1123C>T (p.His375Tyr)	TRIM10 (H375Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367640	NM_006778.4(TRIM10):c.1085G>C (p.Gly362Ala)	TRIM10 (G362A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381461	NM_006778.4(TRIM10):c.1066G>T (p.Ala356Ser)	TRIM10 (A356S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465742	NM_006778.4(TRIM10):c.1064T>C (p.Leu355Pro)	TRIM10 (L355P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210313	NM_006778.4(TRIM10):c.1033C>A (p.Pro345Thr)	TRIM10 (P345T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257294	NM_006778.4(TRIM10):c.941T>C (p.Leu314Pro)	TRIM10 (L314P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2289138	NM_006778.4(TRIM10):c.912G>T (p.Glu304Asp)	TRIM10 (E304D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409249	NM_006778.4(TRIM10):c.866C>T (p.Pro289Leu)	TRIM10 (P289L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2398198	NM_006778.4(TRIM10):c.806C>T (p.Pro269Leu)	TRIM10 (P269L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284164	NM_006778.4(TRIM10):c.673G>A (p.Val225Ile)	TRIM10 (V225I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3182212	NM_006778.4(TRIM10):c.671T>C (p.Leu224Pro)	TRIM10 (L224P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182211	NM_006778.4(TRIM10):c.603C>A (p.Ser201Arg)	TRIM10 (S201R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 710963	NM_006778.4(TRIM10):c.481C>G (p.Gln161Glu)	TRIM10 (Q161E)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2328276	NM_006778.4(TRIM10):c.440A>G (p.His147Arg)	TRIM10 (H147R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224119	NM_006778.4(TRIM10):c.425A>G (p.Tyr142Cys)	TRIM10 (Y142C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254719	NM_006778.4(TRIM10):c.424T>A (p.Tyr142Asn)	TRIM10 (Y142N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182210	NM_006778.4(TRIM10):c.397C>A (p.Arg133Ser)	TRIM10 (R133S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276403	NM_006778.4(TRIM10):c.381C>G (p.His127Gln)	TRIM10 (H127Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350264	NM_006778.4(TRIM10):c.355G>A (p.Val119Met)	TRIM10 (V119M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226711	NM_006778.4(TRIM10):c.306C>A (p.His102Gln)	TRIM10 (H102Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513072	NM_006778.4(TRIM10):c.232G>A (p.Val78Met)	TRIM10 (V78M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533073	NM_006778.4(TRIM10):c.187C>T (p.Pro63Ser)	TRIM10 (P63S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182235	NM_033229.3(TRIM15):c.7G>A (p.Ala3Thr)	TRIM10, TRIM15 (A3T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308546	NM_033229.3(TRIM15):c.33T>G (p.His11Gln)	TRIM10, TRIM15 (H11Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517400	NM_033229.3(TRIM15):c.97C>T (p.His33Tyr)	TRIM10, TRIM15 (H33Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204865	NM_033229.3(TRIM15):c.110G>C (p.Arg37Pro)	TRIM10, TRIM15 (R37P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328638	NM_033229.3(TRIM15):c.161T>C (p.Ile54Thr)	TRIM10, TRIM15 (I54T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328634	NM_033229.3(TRIM15):c.186G>C (p.Glu62Asp)	TRIM10, TRIM15 (E62D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3328635	NM_033229.3(TRIM15):c.220C>T (p.Pro74Ser)	TRIM10, TRIM15 (P74S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248255	NM_033229.3(TRIM15):c.220C>G (p.Pro74Ala)	TRIM10, TRIM15 (P74A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358150	NM_033229.3(TRIM15):c.229C>T (p.Pro77Ser)	TRIM15, TRIM10 (P77S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3182232	NM_033229.3(TRIM15):c.262G>A (p.Glu88Lys)	TRIM10, TRIM15 (E88K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485427	NM_033229.3(TRIM15):c.267G>T (p.Lys89Asn)	TRIM10, TRIM15 (K89N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808143	GRCh37/hg19 6p22.1(chr6:29730504-30202199)x3	HCG17, HLA-A +9 more	Copy number gain	not provided	GUncertain significance
Select item 1807671	GRCh37/hg19 6p22.1(chr6:29162783-30236331)x3	GABBR1, HCG17 +23 more	Copy number gain	not provided	GUncertain significance
Select item 974733	NC_000006.11:g.28005012_31683185del	ABCF1, ABHD16A +106 more	Deletion	Megacolon	GLikely pathogenic
Select item 625706	GRCh37/hg19 6p22.1-q14.1(chr6:29455465-81447367)	ERVH-3, ETV7 +427 more	Copy number gain	not provided	GPathogenic
Select item 443497	GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)	AARS2, ABCC10 +1028 more	Copy number gain	See cases	GPathogenic
Select item 443496	GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3	RING1, RIOK1 +1028 more	Copy number gain	See cases	GPathogenic

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Items: 51